@article{fd50cd32db604558bbb1757c56ecf8e2,
title = "Persistent liver biochemistry abnormalities are more common in older patients and those with cholestatic drug induced liver injury",
abstract = "OBJECTIVES: The long-term outcomes of patients with drug induced liver injury (DILI) are not well described. The aim of this study was to determine the frequency and severity of persistent liver biochemistry abnormalities in DILI patients followed over 2 years. METHODS: Subjects with evidence of liver injury at 6 months after DILI onset were offered a month 12 and 24 study visit. RESULTS: Amongst the 99 patients with definite, probable, or very likely DILI and available laboratory data at 12 months after DILI onset, 74 (75%) had persistent liver injury (persisters) defined as a serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >1.5×upper limit of normal (ULN) or an alkaline phosphatase >ULN, while 25 (25%) had resolved liver injury (resolvers). On multivariate analysis, month 12 persisters were significantly older (52.6 vs. 43.7 years, P=0.01) and more likely to have a cholestatic lab profile at DILI onset (54 vs. 20%, P<0.01) than resolvers. The month 12 persisters also had significantly poorer SF-36 physical summary scores at DILI onset and throughout follow-up compared with the resolvers (P<0.01). Amongst the 17 subjects with a liver biopsy obtained at a median of 387 days after DILI onset, 9 had chronic cholestasis, 3 had steatohepatitis, and 3 had chronic hepatitis. CONCLUSIONS: In all, 75% of subjects with liver injury at 6 months after DILI onset have laboratory evidence of persistent liver injury during prolonged follow-up. Higher serum alkaline phosphatase levels at presentation and older patient age were independent predictors of persistent liver injury. Subjects with persistent liver injury at 12 months after DILI onset should be carefully monitored and assessed for liver disease progression.",
author = "{DILIN Investigators} and Fontana, {Robert J.} and Hayashi, {Paul H.} and Huiman Barnhart and Kleiner, {David E.} and Reddy, {K. Rajender} and Naga Chalasani and Lee, {William M.} and Andrew Stolz and Thomas Phillips and Jose Serrano and Watkins, {Paul B.}",
note = "Funding Information: Guarantor of the Article: Robert J. Fontana, MD. Specific Author contributions: All of the authors were involved in study concept and design, acquisition of data, analysis and interpretation of data, and critical review of the final draft of the manuscript. Drafting of the manuscript (Robert J. Fontana, Paul H. Hayashi, K. Rajender Reddy, Huiman Barnhart, David E. Kleiner), statistical analyses (Huiman Barnhart, Thomas Phillips), review and finalization (Robert J. Fontana, Paul H. Hayashi, Huiman Barnhart, David E. Kleiner, K. Rajender Reddy, Naga Chalasani, William M. Lee, Andrew Stolz, Jose Serrano, Paul B. Watkins). Financial support: The DILIN Network is structured as a U01 cooperative agreement with funds provided by the National Institute of Diabetes and Digestive and Kidney Diseases under grants: 2U01-DK065176-06 (Duke), 2U01-DK065201-06 (UNC), 2U01-DK065184-06 (Michigan), 2U01-DK065211-06 (Indiana), 5U01DK065193-04 (UConn), 5U01-DK065238-08 (UCSF/CPMC), 1U01-DK083023-01 (UTSW), 1U01-DK083027-01 (TJH/UPenn), 1U01-DK082992-01 (Mayo), 1U01-DK083020-01 (USC). Additional funding is provided by CTSA grants: UL1 RR025761 (Indiana), UL1TR000083 (UNC), UL1 RR024134 (UPenn), UL1 RR024986 (Michigan), UL1 RR024982 (UTSW), UL1 RR024150 (Mayo) and in part by the Intramural Research Program of the NIH, National Cancer Institute. Potential conflicts of interest: Dr Fontana has received research support from Vertex Pharmaceuticals, BMS, Janssen, and Gilead; he has also served as a consultant to Tibotec in the past year. Dr Reddy has received research support from Merck, Gilead, Abbvie, Bristol-MyersSquibb, Janssen, Ikaria, and Genfit and served as an advisor to Merck, Genentech-Roche, Gilead, BMS, Vertex, Janssen, Idenix, and Abbvie. Dr Lee receives research support from BI, BMS, Anadys, Gilead, Vertex, Merck, Roche. Consulting: Lilly, Novartis, GSK. Dr Chalasani has served as a consultant to Merck, Aegerion, BMS, Abbvie, Lilly and Salix over the past 12 months and received financial compensation from these entities. He has received research support from Intercept, Cumberland, Gilead, Enterome and Takeda. Dr{\textquoteright}s Barnhart, Hayashi, Stolz, and Serrano have no conflicts of interest. Publisher Copyright: {\textcopyright} 2015 by the American College of Gastroenterology",
year = "2015",
month = oct,
doi = "10.1038/ajg.2015.283",
language = "English (US)",
volume = "110",
pages = "1450--1459",
journal = "American Journal of Gastroenterology",
issn = "0002-9270",
publisher = "Nature Publishing Group",
number = "10",
}