March 27, 2012

Researchers unravel genetic mechanism of fatty liver disease in obese children

Public release date: 26-Mar-2012

Contact: Karen N. Peart
karen.peart@yale.edu
203-432-1326
Yale University

Obese youths with particular genetic variants may be more prone to fatty liver disease, a leading cause of chronic liver disease in children and adolescents in industrialized countries, according to new findings by Yale School of Medicine researchers.

The study, which focused on three ethnic groups, is published in the March issue of the journal Hepatology.

Led by Nicola Santoro, M.D., associate research scientist in the Department of Pediatrics at Yale School of Medicine, the authors measured the hepatic, or liver, fat content of children using magnetic resonance imaging. The study included 181 Caucasian, 139 African-American and 135 Hispanic children who were, on average, age 13.

"We observed that a common genetic variant known as Patatin-like phospholipase domain containing protein-3 (PNPLA3) working with a regulatory protein called glucokinase (GCKR), was associated with increased triglycerides, very low-density lipoproteins levels, and fatty liver," said Santoro.

Santoro explained that his observations could help unravel the genetic mechanisms that contribute to liver fat metabolism. "This may drive the decisions about future drug targets to treat hypertriglyceridemia and non-alcoholic fatty liver disease," he said.

Childhood obesity is a global health concern. Experts say nonalcoholic fatty liver disease is now the leading cause of chronic liver disease in children and adolescents in industrialized countries.

"Our findings confirm that obese youths with genetic variants in the GCKR and PNPLA3 genes may be more susceptible to fatty liver disease," said Santoro, who is cautious about automatically extending this observation to the overall population.

"Our data refer to a population of obese children and adolescents," he said. "I think that further studies in a larger sample size involving lean subjects and adults may help to further define in more details these associations."

###

Other authors on the study included Clarence K. Zhang, Hongyu Zhao, Andrew J. Pakstis, Grace Kim, Romy Kursawe, Daniel J. Dykas, Allen E. Bale, Cosimo Giannini, Bridget Pierpont, Melissa M. Shaw, Leif Groop, and Sonia Caprio.

The work was also funded, in part, by the Yale Clinical and Translational Science Award grant from the National Center for Research Resources at the National Institutes of Health.

Citation: Hepatology Vol. 55, No. 3 (March 2012)
http://onlinelibrary.wiley.com/doi/10.1002/hep.24806/abstract.

Source

Achillion Pharmaceuticals: Hope, Hype, And Hep C

March 27, 2012

Stephen Simpson

I've followed biotech for a long time now, and I have a hard time thinking of an example of another addressable market like hepatitis C (HCV) where investor interest has just exploded in the space of about a year. Like antisense, monoclonal antibodies, RNAi, genomics, stem cells and every other hot property in biotech, there has been no end of hope, hype, and hucksterism. Although HCV is likely to grow into a very financially significant drug target in the coming years, it's worth wondering just how much of the frenzy today can be justified in long-term valuations.

In particular, I'm curious about Achillion Pharmaceuticals (ACHN) these days. I've watched this stock for a while now and came close to buying on multiple times in the pre-2010 pre-$2 level. I underestimated just how fast this market would heat up, though, and had to re-learn a painful lesson - sometimes, you snooze and you lose.

Achillion jumps out as the only serious HCV play I'm aware of with a market cap below $1 billion (while Idenix (IDIX) is hardly a giant at $1.1 billion). Not only is it relatively small, but it also may be one of the relatively few players with its own home-grown effective combination therapy.

Of course everything Achillion is working on in HCV is still in the clinic and as Gilead (GILD) showed so clearly recently, "surprising" clinical results are not always positive surprises. The end result, then, is that this may be the next Pharmasset or just another biotech destined to flame out.

The Good - Interesting Compounds All Their Own

Achillion has at least two HCV antivirals well worth watching - ACH-1625 and ACH-3102.

ACH-1625 is a potentially pangenotypical NS3 protease inhibitor (PI) that has shown both solid efficacy and encouraging safety in early studies. Showing both strong efficacy and safety thus far, it could perhaps be the backbone for future combination therapies. That said, pangenotypical efficacy is not yet established and the compound still has not gone through a pivotal Phase 3 study.

The good news with antivirals is that, unlikely oncology and anti-inflammatory drugs, efficacy signals in early pilot studies often hold up through pivotal studies. What's more, these studies are relatively easy to enroll and can be completed expeditiously. What that all means for investors is that ACH-1625 could have a relatively quick path to market.

Achillion is also developing ACH-3102, a NS5a inhibitor, and expects to put it in human studies soon. This drug looks like it should be less subject to resistance and the company (as well as bulls) seem more excited about this drug than the more advanced ACH-2928 (also a NS5a inhibitor). Coupled with ACH-1625, this could be a very interesting combo therapy, but it's worth mentioning that almost every drug is interesting to bulls going into Phase 2 studies.

These aren't the only drugs in Achillion's HCV pipeline, and the company does have identified experimental compounds targeting bacterial infections and HIV. It should be noted too that Achillion's HCV pipeline is wholly-owned.

The Bad - Competition, And Expectations, Left Right And Center

Achillion is very definitely not going to be the first company to market with new HCV drugs, and there is apt to be extensive competition in the market. That is not only going to place a premium on the SVR efficacy data and safety profile, but also potentially on the marketing muscle of the company in question.

Since its acquisition of Pharmasset, Gilead was put in the pole position in the race to develop blockbuster HCV drugs. That is, until the company reported Phase 2 data on the superstar-to-be '7977 that showed it is not 100% perfect. Specifically, this Phase 2 study indicated that '7977 may not be effective in null responders (patients who have failed to respond to earlier treatments), and may give new hope to alternate approaches that include a NS5a inhibitor or NS3 protease inhibitor.

That said, a little perspective is in order. Maybe '7977 isn't flawless, but SVR-12 rates of 91% in genotype 1 and 100% in genotypes 2 and 3 in a thus far safe drug is still pretty impressive. Moreover, Gilead is looking at a variety of combination possibilities and while the company would certainly love to have "the one antiviral to rule them all", being a part of a blockbuster combination therapy is not a bad consolation prize.

Along Gilead and Achillion is a host of companies developing therapies and a sea of drugs known more by number than by name.

Bristol-Myers Squibb (BMY) has its NS5a inhibitor daclatasvir well along in studies, a PI ('032), and the NS5b inhibitor it acquired with the Inhibitex deal, as well as other earlier stage compounds. The NS5a inhibitor has shown solid efficacy, and its PI/NS5 combo showed 100% SVR without PEG-interferon or ribavarin.

Of course there are many more. Abbott (ABT) has its own all-oral combination (NS5a and PI), as does Roche (RHHBY.PK), although the efficacy in the Roche compounds has not been as encouraging. Johnson & Johnson (JNJ) has its TMC435 PI that it in-licensed from Medivir, and Boeringher Ingelheim has its PI as well. Indenix has a nucleotide inhibitor and NS5a inhibitor in trials and a non-nuc in preclinical development.

Last and not least are Vertex (VRTX) and Merck (MRK). These companies have brought the two newest HCV drugs to market (Incivek and Victrelis, respectively). Vertex has a PI in trials and two nucleotide inhibitors licensed in from Alios, while Merck's PI has seen a significant setback tied to safety issues.

A Quick Rundown On The Market, Prospects, And Deals

The oft-repeated statistic on HCV says that there are between 130 million and 170 million infected persons around the world. Approximately 4 million of those are in the U.S., with another 5 million the EU. By way of comparison, Brazil is thought to have at least 7 million HCV patients, India at least 10 million, and China 43 million.

Untreated HCV offer leads to severe chronic liver disease (including cirrhosis), but the long-used PEG-interferon and ribavirin therapy (dominated by Roche and Merck) has had success rates of below 50% in long-term usage.

That efficacy underlies a lot of the market expectation on HCV drugs. While the pre-Incivek/Victrelis HCV market was estimated to be about $3 billion (with $2.5 billion of that going to PEG-inteferon), analysts believe better efficacy could drive that figure close to $10 billion in 2016.

Admittedly, that's a large number. It may not be completely out of line, though, if these 90%+ SVR rates hold up in pivotal studies. Offer people with a serious lifelong illness a safer, more effective drug that is also easier to take and you can almost always charge a premium for it. Also, think about it this way - the U.S. and European insurance/payer systems are willing to pay several tens of thousands of dollars for cancer therapies that offer a few extra months of median survival benefit, so there's clearly a willingness to pay for better clinical outcomes.

What's this all mean for Achillion?

I could see ACH-1625 garnering perhaps up to a billion in sales if the early results hold all the way through studies. Moreover, there's the potential to be had from the combo therapy; whether that's in combination with another Achillion drug or a rival compound (like, say, Gilead's '7977). If Achillion could garner $1 billion in sales, that would translate into a fair value of $13 to $18 per share today based upon your forward multiple estimate (6x or 8x).

I'm sure $1 billion in sales will sound too small to Achillion bulls. Fair enough; if the early results hold up, maybe it's an even bigger blockbuster, but it looks like there are going to be a lot of competing therapies on the market and good marketing is going to deliver sales even in inferior compounds.

It may well be the case, though, that Achillion never makes it to the point where its sales matter. I would be quite surprised to see Achillion partner its drugs, but I think a buyout could well happen. Certainly there have been plenty of chatter on that subject, what with Gilead and Bristol-Myers paying up for HCV compounds (and Roche also making some deals of its own).

So how does the M&A scene break out? I don't think Bristol-Myers would need Achillion, and I don't think Gilead would go that route either unless a '7977/ACH-1625 really showed something special. Johnson & Johnson may think it needs non-PI partner compounds and may not want to pay for the overlap between their PI programs.

That said, I think there are a lot of names left that could be interested. Merck arguably needs a better protease inhibitor, and likewise Roche, Abbott, and Vertex may find that they need better compounds than they presently have. Companies like Sanofi (SNY) and GlaxoSmithKline (GSK) aren't doing much here today, but could find Achillion to be a ready-made HCV platform. Odds are, though, that Achillion holds out a bit for a desperate buyer - not because there's anything wrong with its pipeline, but because a desperate Merck or Roche may pony up a better deal if they feel pressure.

The Bottom Line

Taking a midpoint of that earlier $13-$18 range, I'd say Achillion may be worth about $15.50 a share today. Annoyingly, that's almost spot on with the current consensus number. I do believe there could be more upside as its pipeline matures and rivals run into problems, but I usually want more than 50% undervaluation before buying into a new biotech story.

Disclosure: I am long RHHBY.PK.

Source

March 26, 2012

VICTRELIS™ Now Available for Eligible Patients in British Columbia

PR-Logo-Newswire

PRESS RELEAE

March 26, 2012, 4:42 p.m. EDT

MONTREAL, March 26, 2012 /PRNewswire via COMTEX/ -- Province to reimburse new chronic hepatitis C treatment

BC PharmaCare recently announced the reimbursement of VICTRELIS™ (boceprevir) for eligible British Columbians living with chronic hepatitis C.

Boceprevir is a first-in-class oral hepatitis C virus (HCV) protease inhibitor for the treatment of chronic hepatitis C genotype 1 infection. It is to be used in combination with peginterferon alpha and ribavirin (peg/riba) in adult patients (18 years and older) with compensated liver disease, including cirrhosis, who are previously untreated or who have failed previous therapy.1 When added to peg/riba, boceprevir can significantly increase a patient's chance of clearing the virus from the body.2,3 The treatment was authorized for use in Canada in July 2011.

"This is most welcome news as British Columbia has one of the heaviest burdens of chronic hepatitis C in Canada," says Dr. Eric Yoshida, hepatologist and Professor of Medicine at the University of British Columbia. "Boceprevir represents a major advance in the treatment of this infection. We now have the ability to cure this disease for a majority of patients, and therefore reduce the risk of premature mortality from end-stage cirrhosis and liver cancer. British Columbia is the third province to offer patients with chronic hepatitis C infection public access to this potentially life-saving treatment."

Eligibility criteria for boceprevir can be accessed through the following link: http://www.health.gov.bc.ca/pharmacare/sa/criteria/restricted/boceprevir.html

Hepatitis C in Canada and British Columbia An estimated 250,000 individuals in Canada are infected with HCV and there are 3,200 to 5,000 newly infected individuals each year.4 About 2,500 new cases of HCV are identified in British Columbia each year.5 HCV damages the liver and may lead to serious complications, including death, when left untreated.6 It is the leading cause of liver transplants in Canada.7

About Merck Today's Merck is a global healthcare leader working to help the world be well. Merck is known as MSD outside the United States and Canada. Through our medicines, vaccines, biologic therapies, and consumer and animal products, we work with customers and operate in more than 140 countries to deliver innovative health solutions. We also demonstrate our commitment to increasing access to healthcare through far-reaching policies, programs and partnerships. For more information about our operations in Canada, visit www.merck.ca .

Forward-Looking Statement This news release includes "forward-looking statements" within the meaning of the safe harbor provisions of the United States Private Securities Litigation Reform Act of 1995. Such statements may include, but are not limited to, statements about the benefits of the merger between Merck and Schering-Plough, including future financial and operating results, the combined company's plans, objectives, expectations and intentions and other statements that are not historical facts. Such statements are based upon the current beliefs and expectations of Merck's management and are subject to significant risks and uncertainties. Actual results may differ from those set forth in the forward-looking statements.

The following factors, among others, could cause actual results to differ from those set forth in the forward-looking statements: the possibility that the expected synergies from the merger of Merck and Schering-Plough will not be realized, or will not be realized within the expected time period; the impact of pharmaceutical industry regulation and health care legislation; the risk that the businesses will not be integrated successfully; disruption from the merger making it more difficult to maintain business and operational relationships.

Merck's ability to accurately predict future market conditions; dependence on the effectiveness of Merck's patents and other protections for innovative products; the risk of new and changing regulation and health policies in the United States and internationally and the exposure to litigation and/or regulatory actions.

Merck undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise. Additional factors that could cause results to differ materially from those described in the forward-looking statements can be found in Merck's 2011 Annual Report on Form 10-K and the company's other filings with the Securities and Exchange Commission (SEC) available at the SEC's Internet site ( www.sec.gov ).

TM Trademark of Schering Corporation, a subsidiary of Merck & Co., Inc. Used under license.

1VICTRELIS™, Product Monograph, July 27, 2011, p. 3. 2Poordad, F., et al., for the SPRINT-2 Investigators. Boceprevir for Untreated Chronic HCV Genotype 1 Infection. N Engl J Med 2011; 364:1195-1206, page 1195. 3Bacon, B.R., et al., for the HCV RESPOND-2 Investigators. Boceprevir for Previously Treated Chronic HCV Genotype 1 Infection. N Engl J Med 2011; 364:1207-1217, p. 1207. 4Canadian Institutes of Health Research. About the Hep C Research Initiative. http://www.cihr-irsc.gc.ca/e/38855.html . Accessed November 2, 2011. 5 HealthLinkBC. http://www.healthlinkbc.ca/dietitian/hfile40a.stm . Accessed March 15, 2011. 6Public Health Agency of Canada. http://www.phac-aspc.gc.ca/hepc/pubs/multiling-hepc/index-eng.php . Accessed November 2, 2011. 7Canadian Liver Foundation. http://www.liver.ca/Liver_Disease/ . Accessed November 2, 2011.

SOURCE MERCK

Source

March 25, 2012

Hepatitis C: From Bed to Book

LucindaPorter

Lucinda K. Porter, RN

Thinking about hepatitis C as a journey may be a metaphor that is overused, but it best describes my experience of living with this disease. My journey is from bed to book, how at my lowest, a virus brought me to this amazing life.

For more than 20 years, mental illness gripped me like a straightjacket (and yes, I know all too well, what a straightjacket feels like). In 1988, unable to bear another moment, I made my final suicide attempt. I had multi-organ failure, including liver failure, and told to say my good-byes, as I would not live another 24 hours.

A miracle, the kindness of others, and a blood transfusion gave me back my life. Why it took this much drama to wake me up to life, I don’t know. What I do know is that my life began in 1988 in that hospital bed. Here is where I slowly emerged from mental illness, physical decay, and soul-sickness. Here is where I started to put back my life, cell by cell, moment by moment.

Hepatitis C virus (HCV) was part of the deal, an unintended consequence of the life-saving transfusion. This virus has been a great gift to me. It reminds me to take care of myself. It is like a mantra, whispering, “Don’t drink. Meditate. Eat well. Go to bed early. Have fun. Help others. Be grateful. Trust the process.”

I went to nursing school, later working at a needle exchange site while undergoing interferon treatment. In 1998, I started writing for the Hepatitis C Support Project (www.hcvadvocate.org) and then landed a job as a hepatology nurse at Stanford Medical Center. I lectured across North America, continued to write and underwent peginterferon plus ribavirin treatment in 2003, but relapsed after treatment ended.

I know HCV inside and out; it is my life’s work. HCV binds me to others, and walking through treatment with patients is a deep privilege. This connection inspired me to write a book, Freedom from Hepatitis C. This guide focuses on helping patients through treatment. I wrote it because it seemed the most expedient way to pass along the knowledge I’ve compiled from my personal experience and what I learned from patients.

I know that some people can’t or don’t want to go through HCV treatment. This does not mean giving up. In fact, having HCV is an argument for doing more to take care of ourselves. Freedom from Hepatitis C suggests ways to maximize one’s health while living with this virus.

I fully intend to undergo treatment again. The “let’s get this taken care of” side of me wants to start now, but my medical team advised me to wait to see what is around the bend. Waiting is hard for me, but since I trust my advisors, I will take their advice. Waiting is a good spiritual practice for me.

The most radical change that I’ve experienced since 1988 is that I don’t let fear rule me. I still feel fear from time to time, but I deal with it. If I could give one thing to people who have HCV,

it would be this: Don’t let fear stop you from anything—from treatment, from joy, or from living a full life.

Free from Hepatitis C is my belief that just about anyone can endure hepatitis C and its treatment. If I, mentally ill, damaged, and hopeless, can go from bed to book, then so can you. You don’t have to be strong or special, you just have to be supported and informed. You don’t have to be especially brave, you just need to be honest and willing. Help is here, for anyone willing to accept it.

Breakthrough could lead to cure for chronic liver disease

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By Steve Connor

Monday March 05 2012

MEDICAL scientists have taken an important step towards understanding how the diseased liver can repair itself in a breakthrough that could eventually lead to the development of new treatments for chronic liver illnesses, which at present can only be cured by organ transplants.

The researchers have worked out how to stimulate the production of vital liver cells known as hepatocytes which are lost when the liver is attacked by potentially fatal conditions such as cirrhosis or chronic hepatitis.

Liver disease is the fifth biggest killer in Britain and is the only major cause of death that has seen a continual year-on-year increase over the past 40 years – more than twice as many people die of liver disease now compared with 20 years ago.

About 16,000 people in the UK died last year of liver disease, and the number of people on the waiting list for organ transplants has increased from about 300 five years ago to nearly 500 now.

The latest research, published in the journal Nature Medicine, has unravelled the network of complex biochemical signals that trigger the regeneration of cells within the liver, the body's main organ for filtering harmful toxins from the bloodstream.

Although the human liver has remarkable powers of natural regeneration, this often results in the replacement of the wrong kind of liver cells. Instead of hepatocytes, the damaged liver tends to make to many bile duct cells, the scientists said.

The scientists were able to shift the balance towards making more hepatocytes by altering the expression of certain genes at the earliest stages of liver cell development. The discovery could lead to the development of drugs that perform the same function in patients, they said.

Luke Boulter of the Medical Research Council's Centre for Regenerative Medicine at Edinburgh University, and lead author of the study, said that understanding how new liver cells are regenerated is key to finding ways of repairing damaged liver tissue.

"This research helps us to know how to increase numbers of cells that are needed for healthy liver function and could pave the way to finding drugs that help liver repair," Dr Boulter said.

Professor Stuart Forbes, associate director of the Centre for Regenerative Medicine, said such studies are needed to tackle the increase in demand for liver transplants. "But the supply of donated organs is not keeping pace with the demand. If we can find ways to encourage the liver to heal itself then we could ease the pressure on waiting lists."

- Steve Connor

Source

A Mother's Heartbreaking Story About Pediatric AIDS

Suzan Stirling

Ambassador, Elizabeth Glaser Pediatric AIDS Foundation

Posted: 03/23/2012 3:29 pm

My name is Suzan. I'm an ambassador for the Elizabeth Glaser Pediatric AIDS Foundation, where I advocate for people to join the fight of mothers around the world to protect their children from HIV. I'm also the author of The Silence of Mercy Bleu -- a story about a young woman who grows up harboring the secret of AIDS.

When people ask me what propelled me to write a novel about HIV/AIDS, they're often surprised to learn that I am a 26-year survivor of the disease. But unlike my character, Mercy, who grows up with the disease and later strives to have a healthy baby, I didn't learn the truth until it was almost too late.

I met and married the love of my life in 1988, and a couple of years later we decided to start a family. In 1990, our wish came true and we welcomed a beautiful baby girl into our lives. In those early years, everything was perfect.

But then in 1996, shortly after the birth of our second child, something began to go terribly wrong. In the matter of a few months, both of our children became very sick.

Alee, our then 5 year-old daughter, began to rapidly lose weight. At the same time, our newborn baby, Mitch, had to be put on a respirator in the ICU, where he would spend weeks fighting a respiratory virus his young body couldn't fend off.

The doctors were candid -- things weren't looking good. There were numerous tests and long hospital stays, but still we had no answers. It was a parent's worst nightmare. We were losing both of our children and no one could tell us why.

I'll never forget the phone call that saved my children's lives. It was a new doctor. She was quick to the point. She said, "Something in your son's blood work warrants an AIDS test. I suggest your whole family be tested."

I was in complete shock. I just remember thinking, "I'm going to have to watch my children die." I didn't think I was strong enough to handle that.

We took our HIV tests, and tragically, our doctor was dead on. I tested positive for HIV. So did Alee and Mitch. We were very lucky in that my husband was negative.

Almost overnight, my family became just another face of AIDS.

It wasn't hard to trace where I'd contracted the virus. Before I'd met my husband, I'd been engaged to a young man who I was later told had died of cancer, but who I now believe died of AIDS. I had carried the virus for nearly 10 years without ever knowing it.

My husband and I nearly lost Alee and Mitchell that year, but 1996 -- the year we were diagnosed -- was also the same year that protease inhibitors became available. My husband and I would crush the blue pills into pudding, clap and cheer, and somehow our children would manage to swallow the brown, sticky mess.

Daily, we saw improvements. This new medicine, in combination with two others, literally brought our children back to us. It was and still is the most miraculous thing that I have ever witnessed.

People often ask me how HIV has changed me, and I almost want to say, "How has it not changed me?" To be completely honest, you can't go through what I've been through -- any life-threatening illness really -- and not come out a completely changed person. HIV is even more difficult because it's a disease that many people suffer with in silence, myself included, for many years.

There were so many things that my family and I had to work through to get to where we are today. HIV forced me to be a much braver, more open person, and I'm thankful for that.

It's never easy for me to share my story, but I think it's important for me -- especially as a mother -- to do so. Today, with medicines that drive the virus to undetectable levels, there is now more hope than ever of staying healthy and stopping HIV transmission. This means being able to protect your partner from the virus, and being able to have a child born free of HIV.

My husband and I were fortunate. We didn't lose our children. The same can't be said for families in other parts of the world, like Africa where our youngest son Yonas was born.

Every day around the world, one thousand mothers -- many of them unaware that they carry HIV-transmit the virus to their own babies in utero, during labor, or through breastfeeding. Without access to the right medicines, they are helpless to protect their own health and that of their babies. Being a mother with three children who are all positive, yet remarkably healthy, I can only imagine what that feels like.

The hardest part of my having HIV was never that I might die -- the hardest part was that I had given this terrible disease to my children. No mother should have to carry that burden. Not today, not ever. Especially when mother-to-child transmission of HIV is completely preventable. With preventative services, the chances of a mother passing the virus on to her children are extremely low -- less than 2 percent. Those are some pretty terrific odds.

We can stop mothers and their children from dying. Really, we can. I know because I've seen it with my own eyes, with my own family.

It's been 16 years now since my children's health was restored. I will get to see my children grow up, and I know that for a parent, there's no greater gift.

As an ambassador for the Elizabeth Glaser Pediatric AIDS Foundation, I get the privilege of joining in the fight to eliminate pediatric AIDS. The work done by the Foundation and its partners around the world is saving children's lives and sparing families unimaginable heartache.

The Foundation has made huge strides to help mothers like me, and lifesaving medicines are now reaching more people than ever. You can be a part of that progress.

Join the fight of mothers around the world, and help us get closer to a new generation born free of HIV.

Source

March 23, 2012

The Affordable Care Act: Our Second Most Important Tool for Combating HIV and Ending AIDS

Posted: 03/23/2012 7:49 pm

As the nation turns its eyes toward the Supreme Court and its review of the Patient Protection and Affordable Care Act (the "ACA") this coming week, people living with HIV and their advocates will be among those watching carefully and most anxiously awaiting the outcome. For many of the approximately 1.2 million people with HIV in this country, the Court's decisions will directly affect access to quality care and life-saving treatment. Though not by any means the only group with a great deal at stake here, those affected by HIV present an exceptionally strong example of the positive impact the ACA will have, and a particularly compelling argument for the statute's constitutionality.

People living with HIV have been systematically excluded from the health-care insurance and health-care markets. Only 17 percent of people living with HIV have private health insurance, compared with 67 percent of the general population. While some of the remaining 83 percent have insurance through public programs (e.g., Medicare, Medicaid, the VA, etc.), nearly 30 percent are forced to rely exclusively upon the often spotty benefits provided through the overburdened and underfunded Ryan White programs, or to go without care altogether.

The consequences of this patchwork quilt of health care for people living with HIV are devastating: they discover their status later, go longer without lifesaving care and treatment, suffer greater complications and poorer health outcomes, and continue to die at frustratingly high and unnecessary rates. These negative consequences are more pronounced and concentrated in already marginalized populations, such as low-income communities; the gay, bisexual, and transgender communities; and communities of color -- most acutely, the black community.

We have at our disposal the means to avoid many of these consequences. Antiretroviral medications (ARVs) provide us with the opportunity to seriously impede progression of the disease, especially when it is discovered in a timely fashion, to prevent most of the complications and poor health outcomes associated with an AIDS diagnosis, and to dramatically reduce the number of AIDS-related deaths each year. For those with access to consistent, quality care and treatment, HIV can now be a chronic, manageable condition -- akin to diabetes or high blood pressure.

What's more, quality care and effective treatment for those currently living with HIV will significantly curtail the further spread of HIV. ARVs work by reducing the level of virus in a person's blood to extremely low levels -- and the less virus in the blood, the lower the chances of transmitting the disease. Recent studies show that the already-lower-than-generally-realized risk of contracting HIV sexually is reduced by up to 96 percent when a person's viral load is suppressed to undetectable levels. Not only is near-universal access to quality health care good for people living with HIV, but it is also one of the best prevention tools we have.

The positive effects of the ACA and the near-universal access to health care it will provide to people living with HIV by 2015 are not just theoretical. Massachusetts, where health-care reform similar to the ACA was enacted years ago, experienced a 37-percent reduction in new HIV infections from 2005 to 2008, while the rest of the country experienced an 8-percent increase. And Massachusetts's age-adjusted HIV/AIDS death rate is almost half the national average (2 percent vs. 3.7 percent). These statistics, and the improved circumstances they describe, foretell what the nation can expect when the ACA is fully implemented.

When viewed through the prism of the HIV/AIDS epidemic, the argument for the constitutionality of the ACA's minimum coverage requirement (or "individual mandate") is relatively simple. Congress has the power to address the exclusion of a particular group -- specifically people living with HIV, but more broadly anyone with a pre-existing condition -- from a market that operates in interstate commerce. But the ban on preexisting condition exclusions will not work without the accompanying individual mandate, which requires every American to become a part of the health-care insurance pool regardless of their current health status. For that reason, the individual mandate is a necessary and proper means by which Congress can effectuate its clearly constitutional power to regulate an interstate market under the Commerce Clause.

Full implementation of the ACA is absolutely critical in our battle against HIV/AIDS. Public health authorities are already talking about the "end of AIDS," meaning the ability to prevent a person's progression from HIV-positive to an AIDS diagnosis and the most detrimental effects of the disease. Let's hope the Supreme Court recognizes the constitutionality of the action Congress took when it passed the ACA, which will similarly prevent our nation's broken health-care system from going from bad to worse -- not just for people living with HIV but for all of us.

For a more detailed explanation of the legal arguments discussed above, read the friend-of-the-court brief submitted by Lambda Legal on behalf of 16 HIV advocacy groups, which was subsequently endorsed by 130 more groups.

Source

9 Simple Ways to Boost Your Liver

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Michelle Schoffro Cook June 23, 2011 3:01 pm

The liver is the body’s main fat-digesting and detoxification organ. Every molecule of fat that you eat must pass through your liver, but if your liver is overburdened by its more than 500 other essential activities, it can become sluggish. Here are ways to boost your liver function:

1. Since the liver requires high amounts of vitamins and minerals to perform its many functions, your diet should be high in fruits and vegetables and nutrient-rich foods.

2. Because food additives and preservatives need to be filtered by your liver, your diet should be free of processed foods, artificial food additives, colors, and preservatives to take the load off your liver. Additionally, choose to eat a diet low in refined sugar and synthetic sweeteners.

3. You should definitely be avoiding margarine, shortening, commercial oils (choose unrefined oils from the refrigerator section of your local health food store). Avoid eating animal fat and fried foods as well.

4. Drink between eight to ten glasses of pure, filtered water every day. This is the only way your liver can flush toxins out of your body.

5. Better yet, start every day with a large glass of water with the fresh juice of one-half to one lemon added. Lemon helps bolster you liver’s detoxification abilities.

6. Eat plenty of liver-rebuilding foods, including: carrots, beets, leafy greens, and other green vegetables.

7. Eat lots of garlic, onions and broccoli since these foods contain sulfur that is required to increase the liver’s detoxification ability.

8. Detoxification in the liver requires considerable amounts of nutrients to function properly so be sure to take a high quality multivitamin and mineral supplement. Even a single nutrient deficiency can seriously disrupt natural detoxification processes.

9. While lying flat on your back, you can gently massage the liver/gallbladder area, which is located along the lower rib area on the right side of your body. This helps improve circulation to the area.

Always consult your physician prior to making dietary changes or taking nutritional supplements.

Source

Hepatitis C Treatment for Drug Users

March 23, 2012

The stigma surrounding addiction may discourage Hepatitis C treatment for drug users - but the evidence encourages these individuals to do triple therapy.

By Nicole Cutler, L.Ac.

Across a variety of cultures, the ability to receive quality medical treatment is not uniform. Unfortunate for some with chronic Hepatitis C, access to the latest drugs can be unjustly withheld. Having health insurance coverage, being considered a good candidate for treatment and assumption of a low relapse risk can be determining factors in who gets the most advanced medications for fighting the Hepatitis C virus. Despite being a population particularly inundated by this viral infection of the liver, intravenous drug users are often excluded from the latest approved Hepatitis C drug regimen.

Clinically acknowledged as a disabling disease, drug addiction is found in every socioeconomic class, within every ethnic group and gender. Addicts typically have extremely strong physiological and psychological cravings to use drugs despite their negative effects. The cravings can be as strong as a human's desire for food and water. Society imposes stigma on addicts because many still believe that addiction is a character flaw or weakness that is incurable. Despite addiction being a treatable disease, the stigma against addicts remains deeply rooted.

Click here to continue reading full article …

AASLD Grant Supports Hepatitis Projects in Mongolia

AASLD News: March 22, 2012

AASLD recently provided a grant in support of the Flagstaff International Relief Effort’s (FIRE) hepatitis related projects in Mongolia.

FIRE is dedicated to providing resources and support to individuals and communities in need, from poverty, political instability, or natural disasters. Their programs are currently focused in Mongolia, an area of the world that a recent article in the Lancet concluded "…has the world's highest rate of liver cancer (deaths) - six times the global average - and the number is increasing..." According to the World Health Organization, "…one of every ten deaths in the country is due to HCC (hepatocellular carcinoma or liver cancer) or its frequent precursor, cirrhosis. In the absence of a solid understanding of this epidemiology, the country's hepatitis C prevalence continues to rise…" Seldom do we hear about these silent tragedies. One of FIRE's missions is to get the message out to the world and to make a change.
With funding from AASLD and other organizations, FIRE has since August been able to:

  • Test 400 health care workers for hepatitis B
  • Send 300 samples to NIH for testing and epidemiological study of hepatitis B, C and D
  • Facilitate the vaccination of 400 selected health care workers for hepatitis B
  • Facilitate the distribution of 20,000 sharps containers

FIRE’s goals for the spring and summer of 2012 are to:

  • Complete a training video for health care workers on health safety practices and hepatitis prevention
  • Facilitate the distribution of 40,000 sharps containers
  • Train 200 health care workers on hepatitis prevention
  • Send 500 blood samples to NIH to conduct testing and epidemiological study of hepatitis B, C, and D
  • Continue the development of a new project with the National Cancer Institute (NCI), a division of NIH, addressing liver cancer

To learn more about FIRE’s hepatitis related projects in Mongolia visit www.fireprojects.org

Source

Studies see link between HIV and abuse among women

ba-hiv22_SFC0108483825_part6

Steptoe now sees her medication regimen as prolonging her life

Liz Hafalia / The Chronicle

Erin Allday

Friday, March 23, 2012

Diagnosed with HIV in the late 1980s, Cassandra Steptoe didn't tell anyone for years, and she didn't get any treatment.

She was depressed and hopeless after a lifetime of physical and sexual abuse. She assumed the infection would kill her. But, somehow, she survived - not just the HIV infection, but far more.

During the past decade, she's received help overcoming the trauma from the years of abuse, and in turn, she's finally faced her HIV diagnosis. And she is far healthier for it, she says.

"I'm a stronger person, a better person, than I was before," said Steptoe, who started treatment in 2003 at the Women's HIV Program at UCSF. "Now when I look at my pills, it's like another day of life."

Steptoe's story - especially her history of trauma and abuse - is hardly unique among women with HIV and AIDS, say doctors and public health experts. In fact, trauma and post-traumatic stress syndrome are closely tied both to the risk of becoming infected with HIV and lower rates of successful treatment, according to two recent UCSF studies.

Address the trauma

And health care providers could better serve many of their female HIV patients if they tackled trauma at the same time as the infection, said Dr. Edward Machtinger, director of the Women's HIV Program and lead author of the studies.

"Screening and responding to trauma needs to be a core element of health care for HIV-positive women, alongside medication and CD4 counts and viral load," Machtinger said.

Machtinger's studies were published this month in the journal AIDS and Behavior. The first study, an analysis of 29 previous reports, found that HIV-positive women were two to six times more likely to have suffered trauma or post-traumatic stress than women without HIV.

According to the study, roughly 30 percent of women with HIV have PTSD - six times the rate of PTSD in the general population of women. More than 60 percent of HIV-positive women have experienced sexual abuse in their lives, compared with 12 percent of women overall, and 55 percent of women with HIV have been a victim of domestic violence, compared with 25 percent of women overall.

The second study looked at patients in UCSF's Women's HIV Program. Based on surveys given to 113 patients, women who had suffered a recent trauma were four times more likely than women who hadn't suffered a trauma to have detectable levels of virus in their blood - meaning that their drug treatment wasn't working.

Those women were also nearly four times more likely than their peers to have unprotected sex with someone who wasn't infected with HIV - or whose status was unknown.

"It appears to us that trauma fuels the HIV epidemic among women," Machtinger said.

A common thread

Health care providers who work with HIV-positive women said physical and sexual abuse is without question common. And when women have experienced a very recent trauma or are in an abusive relationship, the effect on their HIV treatment can be disastrous.

These women may suffer depression or self-esteem issues that make it difficult for them to seek treatment, health care providers said. Or women in an abusive relationship may have partners who won't let them see doctors or pick up their medications.

In many cases, women haven't told their partners that they are HIV-positive, which makes it more difficult to get treatment, said Mary Lawrence Hicks, a nurse practitioner at San Francisco General Hospital who works in the women's HIV clinic there.

"These (HIV) meds must be taken at least on a once-a-day basis, and that's hard for anyone to maintain," Hick said. "But with the chaotic lifestyles that some folks end up in when there's a lot of trauma, it's very, very difficult."

Like many health care providers who treat HIV patients, Hicks said that working with HIV-positive women requires as much focus on mental health care as traditional medical treatment. Many women-centered HIV clinics have social workers and psychiatrists on staff.

"We can't just say here's the prescription and I'll see you in six months," said Dr. Deborah Cohan, director of the Bay Area Perinatal AIDS Center at San Francisco General Hospital. "That's not a realistic way of taking care of these women, because their lives are much more complicated than that."

Road to recovery

For Steptoe, confronting her past trauma was one of the first steps she needed to take toward treating her HIV. She's lucky, she said, that she lived so long without medical care, even as she watched other women die of AIDS.

After moving to San Francisco in 2001, Steptoe went to UCSF for treatment and met Machtinger. He got her started on antiretroviral drugs and pushed her toward counseling programs. Her self-esteem has skyrocketed, she said.

She's now living with her granddaughter and taking care of them both. Her HIV is under control, and she said she's never felt healthier.

"I want to tell other women, we don't have to be beaten up on or have low self-esteem and no value or respect about our bodies," Steptoe said. "I'm on the right path now."

Erin Allday is a San Francisco Chronicle staff writer. eallday@sfchronicle.com

Source

Investigating the Serotonin-Liver Relationship

March 23rd, 2012

Serotonin, the hormone known to make people happy, may also be deeply involved in liver fibrosis.

By Nicole Cutler, L.Ac.

The human body is a complexity, involving countless amazing feats at every moment. Nowhere is this seemingly miraculous series of events more pronounced than in the liver. An organ subjected to repeated abuse, the liver maintains a remarkable ability to regenerate itself upon incurring cellular damage. A new study published in a peer-reviewed journal has found that a hormone known predominantly for its link to emotional well-being also appears to play a role in liver cell regeneration.

Especially in the presence of the Hepatitis B or C virus, alcoholism, a fatty liver or an autoimmune disease, sometimes the balance required to repair liver cells gets disrupted. This disruption impairs the liver’s regenerative abilities so that it can no longer keep up with relentless liver cell injury – and scars form. The propensity to scar more than repair the cellular damage describes the course of chronic liver disease – and British researchers believe that a well-known hormone could be the key to regaining balance.

Click here to continue reading full article …

March 23, 2012, 8:00 a.m. EDT Nordion to Launch Improved Physician Tools for TheraSphere® Liver Cancer Treatment at SIR Annual Scientific Meeting 2012

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PRESS RELEASE

March 23, 2012, 8:00 a.m. EDT

OTTAWA, March 23, 2012 /PRNewswire via COMTEX/ -- Company will also present expert speakers and introduce new iPad app

Nordion Inc. ,a leading provider of products and services for the prevention, diagnosis and treatment of disease, will be attending the Society for Interventional Radiologists (SIR) Annual Scientific Meeting 2012, taking place March 24-29 in San Francisco. The company will introduce several new or updated physician education tools and resources for TheraSphere®, Nordion's Y-90 microsphere treatment for liver cancer.

"With more than 5,000 physicians, scientists and healthcare professionals in attendance, SIR represents one of the most important annual medical meetings Nordion attends," says Peter Covitz, Nordion Senior Vice President, Innovation. "SIR provides an opportunity to connect directly with our key users, share the latest information about TheraSphere, listen to feedback, and respond to questions firsthand."

Nordion representatives will be at Booth #1234 to talk about TheraSphere. The company will host two "Eat and Be Educated" learning sessions at the booth:

Sunday, March 25, 12:15pm How TheraSphere Y-90 Glass Microspheres Fits in Our Treatment Algorithm Matthew Johnson, MD Professor of Radiology and Surgery Indiana University School of Medicine Indianapolis, IN

Tuesday March 27, 12:15pm TheraSphere Multi-Vessel Delivery Siddharth Padia, MD Assistant Professor, Interventional Radiologist University of Washington - Harbourview Medical Center Seattle, WA

Each session will be followed by a Nordion presentation on how to start a TheraSphere program.

Other Nordion TheraSphere activities at SIR include:

Launch of the:

New custom dose feature in Europe and Canada*

Updated Treatment Window Illustrator tool to assist physicians with dose selection

New animated video demonstrating how TheraSphere works

Preview of the upcoming TheraSphere iPad app

Participation in SIR's Residents in Training program

* Nordion has filed a request with the Food and Drug Administration for approval of the custom dose feature in the United States.

About TheraSphere TheraSphere is a liver cancer therapy that consists of millions of small glass beads (20 to 30 micrometers in diameter) containing radioactive yttrium-90 (Y-90). The product is injected by physicians into the artery of the patient's liver through a catheter, which allows the treatment to be delivered directly to the tumour via blood flow.

In the US, TheraSphere is used to treat patients with unresectable hepatocellular carcinoma (HCC), the most common form of primary liver cancer, and can be used as a bridge to surgery or transplantation in these patients. It is also indicated for the treatment of HCC patients with portal vein thrombosis (PVT). TheraSphere is approved by the U.S. Food and Drug Administration (FDA) under a Humanitarian Device Exemption (HDE). HDE approvals are based on demonstrated safety and probable clinical benefit. However, effectiveness of the indication for use has not been established.

TheraSphere® is used in the European Union and in Canada for the treatment of hepatic neoplasia in patients who have appropriately positioned arterial catheters.

Common side effects include mild to moderate fatigue, pain and nausea for about a week. Physicians describe these symptoms as similar to those of the flu. Some patients experience some loss of appetite and temporary changes in several blood tests. For details on rare or more severe side effects, please refer to the TheraSphere package insert/instructions for use at www.nordion.com/therasphere .

About Nordion Inc. Nordion Inc. is a global health science company that provides market-leading products used for the prevention, diagnosis and treatment of disease. We are a leading provider of medical isotopes, targeted therapies and sterilization technologies that benefit the lives of millions of people in more than 60 countries around the world. Our products are used daily by pharmaceutical and biotechnology companies, medical-device manufacturers, hospitals, clinics and research laboratories. Nordion has more than 500 highly skilled employees in three locations. Find out more at www.nordion.com  and follow us at http://twitter.com/NordionInc  .

SOURCE Nordion Inc.

Source

Largest Comparative Study of Radioembolisation Shows SIR-Spheres Microspheres Significantly Improves Survival for Cancer Patients with Inoperable Liver Tumours

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PRESS RELEASE

March 23, 2012, 10:00 a.m. EDT

ORLANDO, March 23, 2012 /PRNewswire via COMTEX/ -- New Australian Data Provides Further Evidence of Survival Benefit for Radioembolisation

Findings from the largest comparative multi-centre study performed to date using radioembolisation report a significantly prolonged survival benefit following SIR-Spheres microspheres in patients with treatment-refractory liver tumours from colorectal and other cancers. The results of the study were presented today at the 65th Annual Cancer Symposium of the Society of Surgical Oncology, by Associate Professor Lourens Bester, Director of Radiology at St Vincent's Hospital, Sydney.[1]

Radioembolisation, which is also called Selective Internal Radiation Therapy or SIRT, is a novel approach to treating liver tumours using microspheres labelled with radioactive yttrium-90 (90Y). The microspheres are implanted by interventional radiologists to selectively target the tumours with radiation while sparing the remaining healthy liver tissue.

Prof. Bester and his colleagues evaluated 463 patients with chemotherapy refractory liver-dominant tumours and found that "radioembolisation is associated with a significantly improved and clinically meaningful survival benefit. Whilst confounding factors may play a role, offering this treatment may confer the best prognosis for these patients," he said.

Among the 251 patients with colorectal liver metastases, median survival in the 220 patients treated with SIR-Spheres microspheres was 11.6 months, compared to only 6.6 months for the 31 patients who received standard or best supportive care (p=0.021). In 212 patients with liver tumours from other cancers, including cholangiocarcinoma (41), neuroendocrine (40), hepatocellular carcinoma (27), pancreatic (13) breast (11), gastric (9) and other cancers (71), median survival was 9.5 months in the 180 patients treated with SIR-Spheres microspheres versus 2.6 months in 32 patients who received standard or best supportive care (p=0.013).

"The significant improvement in overall survival in this study confirm the benefits demonstrated in two previous but smaller comparative studies that were performed in patients with treatment-refractory colorectal liver metastases, notably the multi-centre phase III randomised controlled trial conducted by Hendlisz and colleagues in Belgium, and the matched-pair analysis by Seidensticker and colleagues from Magdeburg, Germany, that reported median survivals of 10.0 and 8.3 months, respectively," Prof. Bester added.[2,3]

Two large international randomised controlled trials are currently underway to evaluate the effectiveness of adding radioembolisation using SIR-Spheres microspheres to first-line chemotherapy in order to assess whether this treatment should be used as an early intervention in the treatment of patients with colorectal cancer liver metastases. In addition, three large randomised controlled trials are evaluating radioembolisation using SIR-Spheres microspheres in hepatocellular carcinoma.

About the study

The aim of the study conducted at St Vincent's Hospital was to compare the outcomes of patients with liver tumours treated using radioembolisation with patients receiving standard or best supportive care alone in the setting of treatment-refractory disease.

All patients had chemotherapy refractory liver-dominant tumours with radiologically confirmed progression, and were no longer qualified for other treatment modalities such as resection, ablation or chemoembolisation.

The study excluded any patient with extensive extrahepatic metastases, symptoms that confined them to bed for more than 50% of the waking hours (ECOG performance status >2), excessive liver tumour burden (>75% of liver replaced by tumour) and/or compromised residual liver function.

Of the 463 patients who underwent initial evaluation for radioembolisation, 63 patients were considered unsuitable, due either to (a) hepatic arterial anatomy that could not be corrected and which could otherwise have led to complications, (b) extensive hepatopulmonary shunting between the liver and lungs, which raised the potential for excess radiation exposure to the lungs (>30 Gy), or (c) reasons relating to patient consent, such as a preference for another treatment option.

"The patients who were unsuitable for radioembolisation were referred back to their treating physician for conservative treatment or continued supportive care," explained Prof Bester. "This group was unlikely to represent patients with more advanced disease and was consequently used as a standard-care comparison cohort."

About Colorectal Cancer

In 2008, 153,000 people in the United States of America and 333,000 in the European Union were diagnosed with colorectal cancer.[4] Around half of these patients will develop metastases that have spread from the original site of the disease, predominately to the liver. Up to 90% of these patients ultimately die from liver failure due to the spread of the disease.

References:

Saxena A, Chua TC, Meteling B et al. Radioembolization with yttrium-90 microspheres is associated with a significantly improved survival compared to conservative therapy after treatment of unresectable hepatic tumors: A large single center experience of 537 patients. 65th Annual Cancer Symposium of the Society of Surgical Oncology, Asia-Pacific Journal of Clinical Oncology 2012; 7 (Supplement s4): Abstract 212.

Hendlisz A, Van den Eynde M, Peeters M et al. Phase III trial comparing protracted intravenous fluorouracil infusion alone or with yttrium-90 resin microspheres radioembolization for liver-limited metastatic colorectal cancer refractory to standard chemotherapy. Journal of Clinical Oncology 2010; 28: 3687-3694.

Seidensticker R, Denecke T, Kraus P et al. Matched-pair comparison of radioembolization plus best supportive care versus best supportive care alone for chemotherapy refractory liver-dominant colorectal metastases. Cardiovascular and Interventional Radiology 2011; ePub doi: 10.1007/s00270-011-0234-7.

International Agency for Research on Cancer. GLOBOCAN 2008: Colorectal Cancer Incidence and Mortality Worldwide in 2008. http://globocan.iarc.fr/factsheets/cancers/colorectal.asp accessed 12/8/2011.

SOURCE St Vincent's Hospital Sydney Limited

Source

Video: Discovery Provides Blueprint for New Drugs That Can Inhibit Hepatitis C Virus



Chemists at the University of California, San Diego have produced the first high resolution structure of a molecule that when attached to the genetic material of the hepatitis C virus prevents it from reproducing. http://ucsdnews.ucsd.edu/pressreleases/discovery_provides_blueprint_for_new_d...

Also See: Discovery provides blueprint for new drugs that can inhibit hepatitis C virus on this blog.

March 22, 2012

How HIV remains a puzzle

skodonnell_-_HIVAIDS

"Even in early infection when the virus population is low, HIV rapidly evolves to evade immune defences and treatments." Image: skodonnell/iStockphoto

The University of Adelaide

Friday, 23 March 2012

New research from the University of Adelaide shows why the development of a cure and new treatments for HIV have been so difficult for scientists to crack.

Dr Jack da Silva from the University's School of Molecular & Biomedical Science has used computer simulations to discover that even in early infection when the virus population is low, HIV rapidly evolves to evade immune defences and treatments.

These results - published in this month's issue of the prestigious journal GENETICS - challenge the commonly held belief that evolution of the virus under these circumstances is very slow.

"I believe the search for a cure for AIDS has failed so far because we do not fully understand how HIV evolves," Dr da Silva said.

To make this discovery, Dr da Silva used computer simulations to determine whether, under realistic conditions, the virus could evolve rapidly if an infection started from a single virus.

This was done by constructing a model of the virus population, then simulating the killing of virus-infected cells by the immune system, along with mutation, recombination (the process by which genetic material is broken and joined to other genetic material), and random genetic changes.

Results show that for realistic rates of cell killing, mutation and recombination, and a realistic population size, the virus could evolve very rapidly even if the initial population size is one.

"At low population levels, viruses have reduced genetic variation and therefore it should be harder for them to evolve rapidly. However, it appears that the evolution of HIV goes against conventional wisdom," Dr da Silva said.

"We now need further insight into the precise genetic mechanisms that enable the virus to so readily adapt to all the challenges we throw at it. Such knowledge will, hopefully, lead to novel strategies for vaccines and other control measures."

Mark Johnston, Editor-in-Chief of GENETICS, said: "Now that we know HIV rapidly evolves, even when its population size is small, we may be able to interfere with its ability to evolve so we can get the most out of the treatments that are developed."

The full report from Dr Jack da Silva can be read online.

Source

Liver cancer patients less likely to die on wait list than candidates without carcinomas

Public release date: 22-Mar-2012

Contact: Dawn Peters
healthnews@wiley.com
781-388-8408
Wiley-Blackwell

Experts call for evaluation of current criteria for allocating organs for transplantation

New research shows increasing disparity in mortality among candidates with and without hepatocellular carcinoma (HCC) who are on the waiting list for liver transplantation. The study available in the April issue of Liver Transplantation, a journal published by Wiley-Blackwell on behalf of the American Association for the Study of Liver Diseases, found that liver cancer patients are less likely to die on the wait list than non-HCC candidates, prompting transplantation specialists to suggest a reevaluation of current allotment criteria for those with HCC.

In 2002, the United Network for Organ Sharing (UNOS) implemented the Model for End Stage Liver Disease (MELD) scoring system to prioritize candidates on the waiting list for liver transplantation in the U.S. While MELD accurately predicts 90-day waitlist mortality, there are some candidates with extensive disease symptoms, such as those with HCC, who need additional prioritizing criteria to assess clinical risk. These candidates receive MELD exception points, of which HCC patients on the wait list could gain 22 points based on increased mortality risk, meaning HCC patients may be transplanted before other patients at greater risk of death.

"With the scarcity of available livers for transplantation, it is vital that allocation criteria ensure those candidates at greatest mortality risk are first to receive a life-saving organ," said Dr. David Goldberg with the University of Pennsylvania and lead author of the current study. "Our study investigated appropriate designation of exception points for transplant candidates with HCC, comparing mortality risk to those with similar MELD scores, but without liver cancer."

The team analyzed data from the Organ Procurement and Transplantation Network (OPTN) UNOS database, including candidates eighteen years of age and older who were on the waiting list for liver transplantation between January 2005 and May 2009. The HCC group was comprised of 6,246 candidates who received exception points for stage two (T2) liver cancer. These candidates were more likely to be older, male and Caucasian or Asian compared to those without liver cancer. In the non-HCC cohort, candidates were categorized by MELD score with 2,564 candidates with a score of 21-23; 4,655 with 24-26; and 2,737 with MELD 27-29.

Analysis shows that within 90 days of listing 4.2% of HCC candidates were removed from the wait list for death or clinical deterioration compared to 11% of non-HCC candidates with MELD scores 21-23. For HCC candidates with 25 exception points (3-6 months wait-time) versus non-HCC candidates with MELD scores 24-26, close to 5% and 17% were removed from the waiting list, respectively. Of the HCC candidates with 28 exception points (6-9 months wait-time) 3% were removed for death or clinical deterioration compared to 24% of non-HCC candidates with MELD scores of 27-29.

Researchers determined that over time the risk of waitlist mortality or clinical decline was unchanged for HCC candidates, but increased significantly for non-HCC candidates. Dr. Goldberg concludes, "Our data suggest HCC candidates have substantially lower odds of waitlist removal for death or deterioration than non-HCC candidates, and strongly indicates that exception points currently allotted for HCC should be lowered."

In a related editorial also published this month in Liver Transplantation, Dr. Patrick Northup from the University of Virginia agrees and writes, "The Goldberg et al. study adds strength to the argument that the 'sickest first' policy may not be well served by the current allocation methods for HCC under the MELD system." He proposes that the transplantation community strive to develop a more fluid allocation system that is responsive to new medical evidence. "The allocation system should be managed as a whole, rather than as isolated pieces, to ensure patients on the waitlist are prioritized based on the desire to minimize waitlist mortality."

###

This study and editorial is published in Liver Transplantation. Media wishing to receive a PDF of the articles may contact healthnews@wiley.com.

Full citations: "Increasing Disparity in Waitlist Mortality Rates with Increased MELD Scores for Candidates with versus without Hepatocellular Carcinoma." David Goldberg, Benjamin French, Peter Abt, Sandy Feng, Andrew M. Cameron. Liver Transplantation; (DOI: 10.1002/lt.23394) Published online: January 23, 2012; Print Issue Date: April 2012. http://onlinelibrary.wiley.com/doi/10.1002/lt.23394/abstract.

Editorial: "HCC and MELD Exceptions: The More We Understand, The More Challenging the Allocation Gets." Patrick G. Northup and Carl L. Berg. Liver Transplantation; (DOI: 10.1002/lt.23409) Published online: Februar 10, 2012; Print Issue Date: April 2012. http://onlinelibrary.wiley.com/doi/10.1002/lt.23409/abstract.

Author Contact: To arrange an interview with Dr. Goldberg, please contact Katie Delach with PENN Medicine at katie.delach@uphs.upenn.edu or 215-349-5964. Media wishing to speak with Dr. Northup may contact Jason Ellis with the University of Virginia at jasonellis@virginia.edu or 434-924-5679.

About the Journal

Liver Transplantation is published by Wiley-Blackwell on behalf of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society. Since the first application of liver transplantation in a clinical situation was reported more than twenty years ago, there has been a great deal of growth in this field and more is anticipated. As an official publication of the AALSD and the ILTS, Liver Transplantation delivers current, peer-reviewed articles on surgical techniques, clinical investigations and drug research — the information necessary to keep abreast of this evolving specialty. For more information, please visit Liver Transplantation.

About Wiley-Blackwell

Wiley-Blackwell is the international scientific, technical, medical, and scholarly publishing business of John Wiley & Sons, with strengths in every major academic and professional field and partnerships with many of the world's leading societies. Wiley-Blackwell publishes nearly 1,500 peer-reviewed journals and 1,500+ new books annually in print and online, as well as databases, major reference works and laboratory protocols. For more information, please visit www.wileyblackwell.com or our new online platform, Wiley Online Library (wileyonlinelibrary.com), one of the world's most extensive multidisciplinary collections of online resources, covering life, health, social and physical sciences, and humanities.

Source

NASTAD: HIV and Viral Hepatitis Policy Watch

Volume 15, March 16, 2012

The Policy Watch provides timely updates and resources on Hill and Administration activities impacting HIV and viral hepatitis programs. Please go to NASTAD's website at www.NASTAD.org for more information.

Congress

FY2013 Budget Resolutions

The House and Senate are currently working on developing budget resolutions for FY2013. The budget resolutions serve as a spending blueprint for all government expenditures, including appropriations. The Budget Control Act set the FY2013 budget level at $1.047 trillion. Despite this level being signed into law, House Republicans are debating lowering the FY2013 spending cap below this level. These additional cuts would impact appropriations as there would be less money for the Labor, Health, and Human Services Appropriations bill which supports HIV and viral hepatitis programs. NASTAD will provide updates as they become available.

FY2013 Appropriations

Representatives Mike Honda (D-CA), Hank Johnson (D-GA) and Judy Chu (D-CA) are circulating a "Dear Colleague" urging Members of Congress to sign on to their letter asking the House Appropriations Committee to support increased funding for the Division of Viral Hepatitis (DVH) at the Centers for Disease Control and Prevention (CDC). The letter reiterates Congress' need to scale-up the viral hepatitis epidemic response in light of rising mortality rates attributable to viral hepatitis in the U.S. over the last decade. According to the letter, "[now] is not the time to be flat-funding this program."

Representative Bill Pascrell, Jr. (D - NJ) is circulating a "Dear Colleague" letter asking for increases in funding for domestic HIV/AIDS programs. The letter emphasizes the need for investments in CDC's HIV prevention program and Ryan White programs.

Additionally, NASTAD has signed on to letters supporting increased funding for domestic programs. The Sexuality Education Coalition letter requests increases for the CDC Division of Adolescent and School Health, including the restoration of funding cut in FY2012, and other sexuality education programs.

Medicaid Block

Grant House Republicans are expected to include a measure to cut and block grant the Medicaid program in their budget proposal. If successful, this effort would dismantle the current federal funding formula for Medicaid allocations and provide a set amount of resources to states, which may be less than they receive now. This proposal was included in the House FY2012 Budget , but was rejected by the Senate. NASTAD, along with the HIV Health Care Access Work Group, is watching this issue closely.

Congressional Inquiry on the 340B Program

Four Members of Congress have sent letters to several organizations including the Safety Net Hospitals for Pharmaceutical Access (SNHPA), which convenes the 340B Coalition, requesting information provided to their membership on specific aspects of the 340B program such as patient definition, contract pharmacies and additional documentation of SNHPA's interaction with their membership. The press release and the letters can be found on Senator Chuck Grassley's (R-IA) website. The 340B program is routinely under Congressional scrutiny, especially after a June Office of Inspector General report found that the program lacked adequate oversight. During the debate on health reform, Republicans advocated terminating the 340B program. NASTAD will continue to monitor Congressional actions related to this vital program.

CDC Hepatitis C Testing Guidelines

Representative Hank Johnson (D-GA) and a bipartisan group of 25 Members of Congress sent a letter to CDC urging the timely release of new testing guidelines for hepatitis C (HCV). The proposed age-based screening guidelines will identify many more Americans with HCV and enable them to access care and treatment, thereby reducing deaths and health care costs associated with the virus.

Administration

Director of the Office of National AIDS Policy (ONAP)

On March 14, the White House named Dr. Grant Colfax as the new director of ONAP. Dr. Colfax currently serves as Director of the HIV Prevention Section in the San Francisco Department of Public Health.

White House LGBT Conference on Housing & Homelessness

On Friday, March 9, 2012, the White House and the U.S. Department of Housing & Urban Development (HUD) held a conference at Wayne State University in Detroit to discuss housing and homelessness issues facing lesbian, gay, bisexual and transgender (LGBT) Americans. The conference drew approximately 125 people, and HUD Secretary Shaun Donovan gave the keynote address reaffirming the Obama administration's commitment to addressing issues with relevance to the LGBT community. Raphael Bostic, Assistant Secretary for Policy Development and Research at HUD, facilitated a workshop on engaging transgender people, LGBT elders and people living with HIV/AIDS. The session focused on keeping homelessness "on the radar screen" among LGBT advocates as attention moves towards implementing the National HIV/AIDS Strategy (NHAS).

2012 White House Policy Briefing for Black LGBT Emerging Leaders

On Friday, February 24, 2012, the White House, in collaboration with the National Black Justice Coalition and the Human Rights Campaign, held a policy briefing for Black LGBT emerging leaders. The 150 participants heard from prominent national Black leaders ranging in topics from safe schools/bullying prevention, HIV/AIDS, faith outreach, and youth entrepreneurship. The HIV/AIDS session, led by Gregorio Millett from the CDC, provided an opportunity for community members to ask questions concerning the shifting landscape of HIV prevention at the federal level and what this means for Black LGBT young people. There was a focus on financial resources and how organizations receiving funding for the population can be held accountable for effective outreach and engagement among Black LGBT communities.

Federal Partners Update

HHS Southern Initiative

HHS is poised to release a demonstration project (using the Secretary's Minority AIDS Initiative funds) to target a set of jurisdictions outside of the 12 cities project. The three year program will focus on reducing health disparities among racial and ethnic minorities in the south, with a particular focus on mortality rates. CDC will disseminate the $14.5 million per year for three years to health departments with a required 25 percent or more of funding to be passed to Community Based Organizations (CBOs). An FOA is in the works and NASTAD will provide more information as it becomes available.

Indicators Update

A memo from HHS Secretary Sebelius directing the heads of Substance Abuse and Mental Health Services Administration (SAMHSA), CDC, Health Resources and Services Administration (HRSA), Office of Minority Health (OMH) and Office on Women's Health (OWH) to adopt a common set of indicators across HHS and streamline the number of grantee data requirements is currently in clearance at HHS. Agencies would have 90 days to finalize standard core metrics. In the subsequent 90 days, HHS would work to develop a plan to operationalize those core indicators and have them fully implemented by the beginning of FY2014. The plan also calls for a 20-25 percent reduction of indicators required for grantees. Andrew Forsyth of the Office of HIV/AIDS Policy presented on this plan at the Presidential Advisory Council on HIV/AIDS (PACHA) meeting on February 29, 2012.

Prevention FOA- Category C

The CDC awarded Category C (demonstration projects) as part of the new health department cooperative agreement, PS 12-1201Comprehensive HIV Prevention Programs for Health Department. Forty nine jurisdictions submitted 71 proposals with 30 jurisdictions receiving funding for a total of $20 million (taken from Category A). Four jurisdictions were awarded between $1 and $2 million; 8 jurisdictions were awarded between $500,000 and $1 million; and 18 jurisdictions were awarded less than $500,000.

NASTAD recently completed a funding memo and analysis of the Category A, core prevention services and Category B, expanded testing awards for PS12-1201.

HHS Viral Hepatitis Testing Consultation

The HHS Office of the Assistant Secretary for Health (ASH) held a consultation on viral hepatitis testing on February 23, 2012 at the Hall of the States. The day-long consultation featured a broad variety of discussions, including challenges to testing, state and local approaches, targeting specific populations as well as discussions with HHS agencies (e.g., SAMHSA) and other key stakeholders (e.g., the Veterans Administration and Departments of Corrections). The consultation was widely attended by federal, non-governmental, advocacy and industry partners, as well as Adult Viral Hepatitis Prevention Coordinators (AVHPCs) and other state health department staff. A meeting summary will be sent out upon availability.

Noteworthy

HAP/NVHR 2012 Viral Hepatitis Policy Summit

The Hepatitis Appropriations Partnership (HAP), which NASTAD convenes, partnered with the National Viral Hepatitis Roundtable (NVHR) for the second year in a row to hold the 2012 Viral Hepatitis Policy Summit. This year's meeting, which is an expansion of the HAP annual face-to-face meeting held in previous years, featured conversations with federal partners from the HHS, CDC, SAMHSA and the Office of Management and Budget (OMB)as well as viral hepatitis Congressional champions. The purpose of the summit was to continue Congressional advocacy while ramping up policy efforts with the Administration.

National Day of Action for Syringe Exchange

With the return of the federal funding ban on Syringe Exchange Programs (SEPs), the Harm Reduction Coalition and their allies are organizing a National Day of Action for Syringe Exchange on March 21, 2012. The day of action will include meetings with Members of Congress, media events to highlight policy and public health issues and a National Call-in Day to highlight opposition to the ban.

Healthcare Reform Monitoring Report

NASTAD partner, Harvard Law School's Treatment Access Expansion Project (TAEP), developed a Healthcare Reform Monitoring Report, which focuses on aspects of Affordable Care Act (ACA) implementation. This can serve as a resource for health department planning for ACA implementation.

Sign-on Letters

NASTAD recently signed on to a letter to the Agency for Healthcare Research and Quality (AHRQ) regarding testing reimbursements.

NASTAD recently signed on to a letter to President Obama in regards to elevating the global and national response to the HIV pandemic by prioritizing the human rights of all persons at risk of and living with HIV.

Legislation of Interest Grid

Here is an updated legislation of interest grid for the most recent HIV, STD and viral hepatitis legislation that we are tracking.

National Alliance of State and Territorial AIDS Directors 444 North Capitol Street, NW • Suite 339 • Washington D.C. 20001 • ph: (202) 434-8090 www.NASTAD.org • em: nastad@nastad.org

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UPDATED EASL Abstracts Embargo Policy

UPDATED International Liver Congress TM 2012 EMBARGO POLICY

International Liver Congress™ 2012 abstracts will be made publicly available on the congress website two weeks in advance of the congress - Wednesday, 04 April 2012. Abstracts posted online on Wednesday, 04 April 2012 are NOT under embargo.

Abstracts selected to be highlighted during official EASL Press Office activities or in official EASL Press Office materials will be made publicly available on the congress website at 1800 (CET) on the day of their presentation at the congress. Abstracts selected to be highlighted during official EASL Press Office activities or in official EASL Press Office materials are under embargo until the date and time of their presentation at the congress.

On Wednesday, 04 April 2012 industry may issue a press release announcing that their abstract has been selected for inclusion in official EASL Press Office activities or in official EASL Press Office materials (abstract title only). Industry must not issue press releases ‑ even under embargo ‑ covering the data contained in abstracts selected to be highlighted during official EASL Press Office activities or in official EASL Press Office materials until the individual embargo for each data set lifts.

Media must not issue coverage of the data contained in abstracts selected to be highlighted during official EASL Press Office activities or in official EASL Press Office materials until the individual embargo for each data set lifts.

Journalists, industry, investigators and/or study sponsors must abide by the embargo times set by EASL.

Violation of the embargo will be taken seriously. Individuals and/or sponsors who violate EASL's embargo policies may face sanctions relating to current and future abstract submissions, presentations and visibility at EASL Congresses. The EASL Governing Board is at liberty to ban attendance and/or retract data.

Copyright for abstracts (both oral and poster) on the website and as made available during The International Liver Congress™ 2012 resides with the respective authors. No reproduction, re-use or transcription for any commercial purpose or use of the content is permitted without the written permission of the authors. Permission for re-use must be obtained directly from the author.

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Liver disease deaths reach record levels in England

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Many of the deaths from liver disease were alcohol related

By Helen Briggs Health editor, BBC News website

Deaths from liver disease in England have reached record levels, rising by 25% in less than a decade, according to new NHS figures.

Heavy drinking, obesity and hepatitis are believed to be behind the rise.

The report by the National End of Life Care Intelligence Network said more deaths were in men, with the highest number of fatalities in the North West.

The number of people who died from liver disease rose from 9,231 in 2001 to 11,575 in 2009, it said.

Other major causes of death, such as heart disease, are declining.

Prof Martin Lombard, national clinical director for liver disease, said: "This report makes for stark reading about the needs of people dying with liver disease.

"Over 70% end up dying in hospital and this report is timely in helping us understand the challenges in managing end-of-life care for this group of people.

"The key drivers for increasing numbers of deaths from liver disease are all preventable, such as alcohol, obesity, hepatitis C and hepatitis B. We must focus our efforts and tackle this problem sooner rather than later."

Several recent reports have warned of rising deaths from liver disease, particularly in the young.

Regional breakdown

  • The age standardised mortality rates per 100,000 people in England were highest in the North West (24), the North East (22) and London (20); and lowest in the East (13), South West (14) and South East (15)

More men

The latest report follows figures published last December which showed a 60% rise in alcoholic liver disease in young people over seven years.

The National End of Life Care Intelligence Network, which analyses death rates and costs of care, looked at statistics for deaths from liver disease across England between 2001 and 2009.

They found most liver deaths were in people under 70, while one in 10 deaths of all people in their 40s were from liver conditions.

Men were disproportionately affected, especially when deaths from liver disease were due to heavy drinking, said the report.

Prof Julia Verne, lead author of the report and clinical lead for the National End of Life Care Intelligence Network, said: "It is crucial that commissioners and providers of health and social care services know the prevalence of liver disease in their local areas, so that more people can receive the care they need to allow them to die in the place of their choosing."

A Department of Health spokesman said: "These figures are a stark reminder of the preventable damage that eating too much and drinking too much alcohol can do.

"Urgent action is needed to halt this trend. Our upcoming liver strategy will set out our plans on this issue, drawing on our plans to tackle problem drinking and obesity."

Andrew Langford, chief executive of the British Liver Trust, said: "This report clearly highlights that liver patients have been, and continue to be, failed by our healthcare system.

"Liver disease has remained the poor relation in comparison to other big killers such as cancer and heart disease, yet liver disease is the only big killer on the rise."

The chief executive of Alcohol Concern, Eric Appleby, said: "This report shows that loss of life through alcoholic liver disease remains as big a problem as ever, with a worrying tendency for those with the highest deprivation to suffer most, leading to a distinct north/south divide.

"Minimum pricing of alcohol should do much to impact on the levels of drinking that lead to alcoholic liver disease, but health service commissioners must prioritise the disease at the local level too, focusing on ways to catch problem drinking early and so help to reduce the huge social and economic cost of the current death rate."

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