Authors: Cross, T. J. S.; Calvaruso, V.1; Foxton, M. R.2; Manousou, P.1; Quaglia, A.2; Grillo, F.1; Dhillon, A. P.1; Nolan, J.2; Chang, T. P.1; O'Grady, J.2; Heneghan, M. A.2; O'Beirne, J. P.1; Burroughs, A. K.1; Harrison, P. M.3
Source: Journal of Viral Hepatitis, Volume 17, Number 9, September 2010 , pp. 640-649(10)
Recurrent hepatitis C is a common cause of graft loss in patients undergoing liver transplantation, and serial protocol liver biopsies have been used to identify patients at risk of graft loss from rapid fibrosis progression. The aim of this study was to derive a simple noninvasive index to predict fibrosis in patients with recurrent hepatitis C post-transplant. A retrospective study was performed assessing serial liver biopsies for post-transplant chronic hepatitis C infection. One hundred eighty-five patients were included in the analysis; median age 53 years (interquartile range 48-59) and 140 (76%) were male. Liver histology showed 53 (29%) had Ishak fibrosis stages F0/F1, 31 (17%) had F2, 29 (16%) had F3, 19 (10%) had F4 and 53 (29%) had F5/F6. The London Transplant Centres' (LTC) score was derived combining aspartate aminotransferase (AST IU/L), time from liver transplant (TFLT months), international normalized ratio and platelets. Diagnostic accuracy of the LTC score was assessed using area under receiver-operating characteristic (ROC) curves. The area under the ROC curve for moderate fibrosis (F ≥ 2) was 0.78 (95% CI, 0.70-0.86; P < 0.0001), for advanced fibrosis (F4-6) was 0.80 (95% CI, 0.72-0.87; P < 0.0001) and for cirrhosis was 0.80 (95% CI, 0.72-0.88; P < 0.0001). An optimal cut-off value of 6.3 distinguished patients with no or mild fibrosis (F ≤ 1) odds ratio 10.8 (95% CI, 5.1-22.9); P < 0.0001), sensitivity 88%, specificity 60%, negative predictive value 67% and positive predictive value 84%. The LTC score can identify patients with Hepatitis C virus recurrence following liver transplant with a low risk of significant fibrosis, thus avoiding the need for protocol biopsy.
Keywords: fibrosis; hepatitis C; liver transplantation; noninvasive marker
Document Type: Research article
Affiliations: 1: Department of Hepatology and Liver Transplantation, The Royal Free Hospital, Pond Street, London, UK 2: Institute of Liver Studies, King's College Hospital, Denmark Hill, London, UK 3: Division of Gene and Cell-based Therapy, Department of Liver Studies and Transplantation, King's College London, Denmark Hill Campus, Bessemer Road, London, UK