Showing posts with label Autoimmune Liver Disease. Show all posts
Showing posts with label Autoimmune Liver Disease. Show all posts

May 18, 2013

Coffee Consumption Associated with Reduced Risk of Autoimmunue Liver Disease

A Range of New Research Studies Presented at DDW® 2013

Orlando, FL (May 18, 2013) — Research presented today at Digestive Disease Week® (DDW) explores new discoveries in liver disease research, with findings about the impact of coffee on autoimmune disease and palliative care for cirrhotic patients.

While coffee consumption recently has been associated with reduced risk of fibrosis, a new study found that even a few more cups of java each month also correlate with lower risk for a particular autoimmune liver disease. Researchers at the Mayo Clinic, Rochester, MN, linked coffee consumption with reduced risk of primary sclerosing cholangitis (PSC), a disease of the bile ducts that causes inflammation and subsequent duct obstruction that ultimately can lead to cirrhosis of the liver, liver failure and biliary cancer.

“While rare, PSC has extremely detrimental effects,” said Craig Lammert, MD, instructor of medicine at Mayo Clinic. “We are always looking for ways to mitigate risk, and our first-time finding points to a novel environmental effect that might also help us to determine the cause of this and other devastating autoimmune diseases.”

Funded by grants from the National Institutes of Health and the American Liver Foundation, the study examined the largest cohort of patients with PSC and primary biliary cirrhosis (PBC) in the U.S. as well as a healthy control group. Data showed that coffee consumption was associated with reduced risk of PSC, but not PBC. PSC patients were much more likely to never consume coffee compared with the control group. The control group also spent nearly 20 percent more of their life regularly drinking coffee.

Study highlights need of terminally ill cirrhotic patients

Other DDW research illuminates the need for better palliative care for terminally ill cirrhotic patients who are rejected for a liver transplant. A retrospective cohort review of patients previously assessed or listed for liver transplant by the University of Alberta in Canada found that only 3 percent of patients in the study died while in hospice, a hallmark of palliative care.

“In our study, less than 10 percent of patients had even been referred to palliative care,” said Constantine Karvellas, assistant professor of medicine at the University of Alberta. “We need to be better about ensuring quality of life for these patients.”

Palliative care is specialized medical care for people with serious, often terminal, illnesses. Its goal is to improve patients’ quality of life by concentrating on relief from symptoms, pain and stress.

The patients in Dr. Karvellas’s study had been de-listed or declined for liver transplantation. The most common reason was noncompliance with restrictions on substance use, but other reasons related to cancer and multiple organ dysfunction. Researchers examined patients’ medical trajectory and the symptoms prominent at their end of life and found that more than half had pain and nausea. Others had symptoms of depression, anxiety, breathlessness and anorexia. Eighty percent required repeat hospital admissions and invasive procedures such as paracentesis, in which fluid accumulation is drained from the abdomen.

“Palliative care offers a way to avoid some of these costly procedures and at the same time improve the quality of life for these patients. This data helps to start the conversation on how we can make a positive difference in the lives of many patients and families,” Dr. Karvellas said.

Dr. Lammert will present data from the study “Coffee consumption is associated with reduced risk of primary sclerosing cholangitis but not primary biliary cirrhosis,” abstract 630, on Monday, May 20, at 10 a.m. ET in Room 205A of the Orange County Convention Center.

Dr. Karvellas will present data from the study “Paucity of palliation in cirrhotic patients: a retrospective study and needs assessment,” abstract 796, on Monday, May 20, at 4:30 p.m. ET in Room 202AB of the Orange County Convention Center.

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Digestive Disease Week® (DDW) is the largest international gathering of physicians, researchers and academics in the fields of gastroenterology, hepatology, endoscopy and gastrointestinal surgery. Jointly sponsored by the American Association for the Study of Liver Diseases (AASLD), the American Gastroenterological Association (AGA) Institute, the American Society for Gastrointestinal Endoscopy (ASGE) and the Society for Surgery of the Alimentary Tract (SSAT), DDW takes place May 18 to 21, 2013, at the Orange County Convention Center, Orlando, FL. The meeting showcases more than 5,000 abstracts and hundreds of lectures on the latest advances in GI research, medicine and technology. More information can be found at www.ddw.org.

Follow us on Twitter @DDWMeeting; hashtag #DDW13. Become a fan of DDW on Facebook.

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September 11, 2012

British researchers uncover genetic clues to common autoimmune liver disease

[Date: 2012-09-11]

A team of scientists has used a new technology to uncover three genetic regions associated with primary biliary cirrhosis (PBC), a chronic and progressive disease of the liver.

The aim of the study was to survey more thoroughly regions of the genome known to underlie other autoimmune diseases, to discover if they also play a role in PBC susceptibility.

Scientists used a DNA microchip called Immunochip in their tests: the advantage of Immunochip over genome-wide technologies is that it focuses only on regions of the genome known to be associated with an autoimmune disease, and thus captures more of the genetic variation within these regions. Immunochip can therefore be used to more thoroughly test these key candidate genes for association to a whole-host of immune-related traits, and to identify low-frequency and rare genetic variants associated with disease that would likely be missed by a microarray covering a broader range of genetic regions.

Writing in the journal Nature Genetics, the researchers outline how they identified three genetic regions associated with PBC, increasing the number of known regions associated with the disorder to 25.

By combining the results from this survey with details of gene activity from a database called ENCODE, they were able to identify which cell types are most likely to play a role in PBC.

PBC affects approximately one in a thousand women over the age of 40. The condition is characterised by inflammation in the bile ducts that blocks the flow of bile, damaging the liver cells and causing further inflammation and scarring. In severe cases, this results in the need for a liver transplant.

As there is currently no cure for PBC, treatment is focused on slowing down the progression of the disease and treating any symptoms or complications that may occur. The biological pathways underlying primary biliary cirrhosis are poorly understood, although autoimmunity, where the body attacks its own cells, is known to play a significant role.

Co-senior author of the study Dr Carl Anderson from the Wellcome Trust Sanger Institute comments: 'Previous genetic screens have identified 22 regions of the genome underlying PBC risk, and many of these are known to play a role in other autoimmune diseases, such as multiple sclerosis and type I diabetes. Using the Immunochip we were able to perform a much more thorough screen of the genomic regions previously associated with other autoimmune diseases. This resulted in us identifying a further three regions involved in PBC risk and identifying additional independent signals within some of those we already knew about.'

The hope is that these results could lead to the development of a new therapeutic approach for the treatment of PBC.

For more information, please visit:
Wellcome Trust Sanger Institute:
http://www.sanger.ac.uk/

Category: Miscellaneous
Data Source Provider: Wellcome Trust Sanger Institute
Document Reference: Liu, J. Z. et al., Dense fine-mapping study identifies novel disease loci and implicates coding and non-coding variation in primary biliary cirrhosis risk, Nature Genetics, 2012. doi:10.1038/ng.2395
Subject Index: Medicine, Health; Life Sciences; Scientific Research

RCN: 35009

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