TY - JOUR
T1 - Features and outcomes of 899 patients with drug-induced liver injury
T2 - The DILIN prospective study
AU - Chalasani, Naga
AU - Bonkovsky, Herbert L.
AU - Fontana, Robert
AU - Lee, William
AU - Stolz, Andrew
AU - Talwalkar, Jayant
AU - Reddy, K. Rajendar
AU - Watkins, Paul B.
AU - Navarro, Victor
AU - Barnhart, Huiman
AU - Gu, Jiezhun
AU - Serrano, Jose
AU - Ahmad, Jawad
AU - Bach, Nancy
AU - Bansal, Meena
AU - Barnhart, Huiman X.
AU - Beavers, Kimberly
AU - Calvo, Francisco O.
AU - Chang, Charissa
AU - Conjeevaram, Hari
AU - Conner, Gregory
AU - Darling, Jama
AU - De Boer, Ynto
AU - Dieterich, Douglas
AU - Dipaola, Frank
AU - Durazo, Francisco A.
AU - Everhart, James E.
AU - Fontana, Robert J.
AU - Ghabril, Marwan S.
AU - Goldstein, David
AU - Gopalreddy, Vani
AU - Grewal, Priya
AU - Hayashi, Paul H.
AU - Hoofnagle, Jay
AU - Kaplowitz, Neil
AU - Liangpunsakul, Suthat
AU - Lichtman, Steven
AU - Liu, Lawrence
AU - Navarro, Victor J.
AU - Odin, Joseph
AU - Rossi, Simona
AU - Russo, Mark
AU - Schiano, Thomas
AU - Sherker, Averell H.
AU - Vuppalanchi, Raj
AU - Zacks, Steven
AU - Balasco, Amanda
AU - Chesney, Kristin
AU - Corne, Audrey
AU - Cummings, Sherrie
AU - Groseclose, Gale
AU - Hammett, Alex
AU - Hooker, Judy
AU - Kesar, Varun
AU - Mao, Sophana
AU - Marks, Kenari
AU - McFadden, Regina
AU - Melgoza, Yolanda
AU - Mikhail, Sherif
AU - Milstein, Susan
AU - Morlan, Wendy
AU - Peacock, Val
AU - Rosado, Nidia
AU - Russell, Tracy
AU - Vega, Maricruz
AU - Verma, Manisha
AU - Walker, Patricia
AU - Yalamanchili, Rachana
AU - McClanahan-Crowder, Michelle
AU - Galan, Katherine
AU - Chau, Tuan
AU - Ragavan, Kowsalya
AU - Rostami, Hoss
AU - Puglisi-Scharenbroich, Carmel
AU - Torrance, Rebecca J.
AU - Van Raaphorst, Rebekah
N1 - Funding Information:
Funding The DILIN ( https://dilin.dcri.duke.edu/ ) is supported by the National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health (NIH) as a Cooperative Agreement (U01s) under grants: U01-DK065176 (Duke), U01-DK065201 (UNC), U01-DK065184 (Michigan), U01-DK065211 (Indiana), U01DK065193 (UConn), U01-DK065238 (UCSF/CPMC), U01-DK083023 (UTSW), U01-DK083027 (TJH/UPenn), U01-DK082992 (Mayo), U01-DK083020 (USC). Additional funding is provided by CTSA Grants: UL1 RR025761 (Indiana), UL1 RR025747 (UNC), UL1 RR024134 (UPenn), UL1 RR024986 (Michigan), UL1 RR024982 (UTSW), UL1 RR024150 (Mayo) and by the Intramural Research Program of the National Cancer Institute, National Institutes of Health (NIH). A complete list of participants in DILIN is given in the Acknowledgments.
Funding Information:
Conflicts of interest These authors disclose the following: Naga P. Chalasani serves as a paid consultant to Abbvie, Salix, Aegerion, Lilly, Mitsubishi Tanabe, Wellpoint, and Boehringer-Ingelheim in the past 12 months and received grant support from Intercept, Cumberland, Gilead, and Galectin. Herbert Bonkovsky has served as a consultant to Alnylam, Clinuvel, Lundbeck, and Recordati in the past 12 months. He has research support from Clinuvel and Vertex. Robert Fontana has received grant support from Gilead and Vertex and served as a paid consultant to Tibotec, Merck and GSK. Paul Watkins served as a paid consultant to Abbvie, Actelion, Amgen, BMS, Boerringer−Ingelheim, Biogen-Idec, BMS, Diaichi-Sankyo, Genzyme, Gilead, GSK, Hoffman-LaRoche, Merck, Janssen, Novartis, Otsuka, Pfizer, Sanolfi-Aventis, and Takeda, in the past 12 months. William Lee served as a consultant to Lilly, Pfizer, and Novartis. He received research support from BMS, GSK, Vertex, and Merck. K. Rajendar Reddy served as a consultant to BMS, Gilead, Abbvie, Merck, Genentech-Roche, Vertex, and Janssen. He has research support from BMS, Abbvie, Gilead, Merck, Genentech-Roche, Vertex, Janssen, and Gen-Fit. Victor Navarro serves on the Data and Safety Monitoring Board for GlaxoSmithKline. The remaining authors disclose no conflicts.
Publisher Copyright:
© 2015 AGA Institute.
PY - 2015/6/1
Y1 - 2015/6/1
N2 - Background & Aims The Drug-Induced Liver Injury Network is conducting a prospective study of patients with DILI in the United States. We present characteristics and subgroup analyses from the first 1257 patients enrolled in the study. Methods In an observational longitudinal study, we began collecting data on eligible individuals with suspected DILI in 2004, following them for 6 months or longer. Subjects were evaluated systematically for other etiologies, causes, and severity of DILI. Results Among 1257 enrolled subjects with suspected DILI, the causality was assessed in 1091 patients, and 899 were considered to have definite, highly likely, or probable DILI. Ten percent of patients died or underwent liver transplantation, and 17% had chronic liver injury. In the 89 patients (10%) with pre-existing liver disease, DILI appeared to be more severe than in those without (difference not statistically significant; P =.09) and mortality was significantly higher (16% vs 5.2%; P <.001). Azithromycin was the implicated agent in a higher proportion of patients with pre-existing liver disease compared with those without liver disease (6.7% vs 1.5%; P =.006). Forty-one cases with latency ≤7 days were caused predominantly by antimicrobial agents (71%). Two most common causes for 60 DILI cases with latency >365 days were nitrofurantoin (25%) or minocycline (17%). There were no differences in outcomes of patients with short vs long latency of DILI. Compared with individuals younger than 65 years, individuals 65 years or older (n = 149) were more likely to have cholestatic injury, although mortality and rate of liver transplantation did not differ. Nine patients (1%) had concomitant severe skin reactions; implicated agents were lamotrigine, azithromycin, carbamazepine, moxifloxacin, cephalexin, diclofenac, and nitrofurantoin. Four of these patients died. Conclusions Mortality from DILI is significantly higher in individuals with pre-existing liver disease or concomitant severe skin reactions compared with patients without. Additional studies are needed to confirm the association between azithromycin and increased DILI in patients with chronic liver disease. Older age and short or long latencies are not associated with DILI mortality.
AB - Background & Aims The Drug-Induced Liver Injury Network is conducting a prospective study of patients with DILI in the United States. We present characteristics and subgroup analyses from the first 1257 patients enrolled in the study. Methods In an observational longitudinal study, we began collecting data on eligible individuals with suspected DILI in 2004, following them for 6 months or longer. Subjects were evaluated systematically for other etiologies, causes, and severity of DILI. Results Among 1257 enrolled subjects with suspected DILI, the causality was assessed in 1091 patients, and 899 were considered to have definite, highly likely, or probable DILI. Ten percent of patients died or underwent liver transplantation, and 17% had chronic liver injury. In the 89 patients (10%) with pre-existing liver disease, DILI appeared to be more severe than in those without (difference not statistically significant; P =.09) and mortality was significantly higher (16% vs 5.2%; P <.001). Azithromycin was the implicated agent in a higher proportion of patients with pre-existing liver disease compared with those without liver disease (6.7% vs 1.5%; P =.006). Forty-one cases with latency ≤7 days were caused predominantly by antimicrobial agents (71%). Two most common causes for 60 DILI cases with latency >365 days were nitrofurantoin (25%) or minocycline (17%). There were no differences in outcomes of patients with short vs long latency of DILI. Compared with individuals younger than 65 years, individuals 65 years or older (n = 149) were more likely to have cholestatic injury, although mortality and rate of liver transplantation did not differ. Nine patients (1%) had concomitant severe skin reactions; implicated agents were lamotrigine, azithromycin, carbamazepine, moxifloxacin, cephalexin, diclofenac, and nitrofurantoin. Four of these patients died. Conclusions Mortality from DILI is significantly higher in individuals with pre-existing liver disease or concomitant severe skin reactions compared with patients without. Additional studies are needed to confirm the association between azithromycin and increased DILI in patients with chronic liver disease. Older age and short or long latencies are not associated with DILI mortality.
KW - DILI
KW - DILIN
KW - Idiosyncratic
KW - Medication
KW - Toxicity
UR - http://www.scopus.com/inward/record.url?scp=84930017409&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84930017409&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2015.03.006
DO - 10.1053/j.gastro.2015.03.006
M3 - Article
C2 - 25754159
AN - SCOPUS:84930017409
SN - 0016-5085
VL - 148
SP - 1340-1352.e7
JO - Gastroenterology
JF - Gastroenterology
IS - 7
ER -