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      Drug-induced liver injury.

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          Abstract

          Drug-induced liver injury (DILI) is an adverse reaction to drugs or other xenobiotics that occurs either as a predictable event when an individual is exposed to toxic doses of some compounds or as an unpredictable event with many drugs in common use. Drugs can be harmful to the liver in susceptible individuals owing to genetic and environmental risk factors. These risk factors modify hepatic metabolism and excretion of the DILI-causative agent leading to cellular stress, cell death, activation of an adaptive immune response and a failure to adapt, with progression to overt liver injury. Idiosyncratic DILI is a relative rare hepatic disorder but can be severe and, in some cases, fatal, presenting with a variety of phenotypes, which mimic other hepatic diseases. The diagnosis of DILI relies on the exclusion of other aetiologies of liver disease as specific biomarkers are still lacking. Clinical scales such as CIOMS/RUCAM can support the diagnostic process but need refinement. A number of clinical variables, validated in prospective cohorts, can be used to predict a more severe DILI outcome. Although no pharmacological therapy has been adequately tested in randomized clinical trials, corticosteroids can be useful, particularly in the emergent form of DILI related to immune-checkpoint inhibitors in patients with cancer.

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          Author and article information

          Journal
          Nat Rev Dis Primers
          Nature reviews. Disease primers
          Springer Science and Business Media LLC
          2056-676X
          2056-676X
          Aug 22 2019
          : 5
          : 1
          Affiliations
          [1 ] Unidad de Gestión Clínica de Enfermedades Digestivas, Instituto de Investigación Biomédica de Málaga-IBIMA, Hospital Universitario Virgen de la Victoria, Universidad de Málaga, Malaga, Spain. andrade@uma.es.
          [2 ] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain. andrade@uma.es.
          [3 ] Division of Gastroenterology, Indiana University School of Medicine, Indianapolis, IN, USA.
          [4 ] Department of Gastroenterology, Landspitali University Hospital Reykjavik, University of Iceland, Reykjavík, Iceland.
          [5 ] Faculty of Medicine, University of Iceland, Reykjavík, Iceland.
          [6 ] Gastroenterology, Duke University, Durham, NC, USA.
          [7 ] Gastroenterology, Durham VA Medical Centre, Durham, NC, USA.
          [8 ] Department of Clinical Pharmacology and Toxicology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
          [9 ] Mechanistic Safety, CMO & Patient Safety, Global Drug Development, Novartis Pharma, Basel, Switzerland.
          [10 ] UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USA.
          [11 ] University of North Carolina Institute for Drug Safety Sciences, Research Triangle Park, Chapel Hill, NC, USA.
          [12 ] Department of Gastroenterology and Hepatology, St. John's Medical College Hospital, Bangalore, India.
          [13 ] Patient Safety, AstraZeneca, Gaithersburg, MD, USA.
          [14 ] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain. lucena@uma.es.
          [15 ] Servicio de Farmacología Clínica, Instituto de Investigación Biomédica de Málaga-IBIMA, Hospital Universitario Virgen de la Victoria, UICEC SCReN, Universidad de Málaga, Málaga, Spain. lucena@uma.es.
          [16 ] Division of Gastroenterology and Liver Diseases, Department of Medicine, Keck School of Medicine, Los Angeles, CA, USA.
          [17 ] National Institute for Health Research (NIHR) Nottingham Digestive Diseases Biomedical Research Centre, Nottingham University Hospital NHS Trust and University of Nottingham, Nottingham, UK.
          Article
          10.1038/s41572-019-0105-0
          10.1038/s41572-019-0105-0
          31439850
          9b577592-99d6-4a88-ac23-6c3ef27381d3
          History

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