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Drug-Induced Liver Injury: Highlights and Controversies in the Recent Literature

Drug-induced liver injury (DILI) remains an important, yet challenging diagnosis for physicians. Each year, additional drugs are implicated in DILI and this year was no different, with more than 1400 articles published on the subject. This review examines some of the most significant highlights and...

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Autores principales: Clinton, Joseph William, Kiparizoska, Sara, Aggarwal, Soorya, Woo, Stephanie, Davis, William, Lewis, James H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447115/
https://www.ncbi.nlm.nih.gov/pubmed/34533782
http://dx.doi.org/10.1007/s40264-021-01109-4
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author Clinton, Joseph William
Kiparizoska, Sara
Aggarwal, Soorya
Woo, Stephanie
Davis, William
Lewis, James H.
author_facet Clinton, Joseph William
Kiparizoska, Sara
Aggarwal, Soorya
Woo, Stephanie
Davis, William
Lewis, James H.
author_sort Clinton, Joseph William
collection PubMed
description Drug-induced liver injury (DILI) remains an important, yet challenging diagnosis for physicians. Each year, additional drugs are implicated in DILI and this year was no different, with more than 1400 articles published on the subject. This review examines some of the most significant highlights and controversies in DILI-related research over the past year and their implications for clinical practice. Several new drugs were approved by the US Food and Drug Administration including a number of drugs implicated in causing DILI, particularly among the chemotherapeutic classes. The COVID-19 pandemic was also a major focus of attention in 2020 and we discuss some of the notable aspects of COVID-19-related liver injury and its implications for diagnosing DILI. Updates in diagnostic and causality assessments related to DILI such as the Roussel Uclaf Causality Assessment Method are included, mindful that there is still no single biomarker or diagnostic tool to unequivocally diagnose DILI. Glutamate dehydrogenase received renewed attention as being more specific than alanine aminotransferase. There were a few new reports of previously unrecognized hepatotoxins, including immune modulators and novel gene therapy drugs that we highlight. Updates and new developments of previously described hepatotoxins, such as immune checkpoint inhibitors and anti-tuberculosis drugs are reviewed. Finally, novel technologies such as organoid culture systems to better predict DILI preclinically may be coming of age and determinants of hepatocyte loss, such as calculating P(ALT) are poised to improve our current means of estimating DILI severity and the risk of acute liver failure.
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spelling pubmed-84471152021-09-17 Drug-Induced Liver Injury: Highlights and Controversies in the Recent Literature Clinton, Joseph William Kiparizoska, Sara Aggarwal, Soorya Woo, Stephanie Davis, William Lewis, James H. Drug Saf Review Article Drug-induced liver injury (DILI) remains an important, yet challenging diagnosis for physicians. Each year, additional drugs are implicated in DILI and this year was no different, with more than 1400 articles published on the subject. This review examines some of the most significant highlights and controversies in DILI-related research over the past year and their implications for clinical practice. Several new drugs were approved by the US Food and Drug Administration including a number of drugs implicated in causing DILI, particularly among the chemotherapeutic classes. The COVID-19 pandemic was also a major focus of attention in 2020 and we discuss some of the notable aspects of COVID-19-related liver injury and its implications for diagnosing DILI. Updates in diagnostic and causality assessments related to DILI such as the Roussel Uclaf Causality Assessment Method are included, mindful that there is still no single biomarker or diagnostic tool to unequivocally diagnose DILI. Glutamate dehydrogenase received renewed attention as being more specific than alanine aminotransferase. There were a few new reports of previously unrecognized hepatotoxins, including immune modulators and novel gene therapy drugs that we highlight. Updates and new developments of previously described hepatotoxins, such as immune checkpoint inhibitors and anti-tuberculosis drugs are reviewed. Finally, novel technologies such as organoid culture systems to better predict DILI preclinically may be coming of age and determinants of hepatocyte loss, such as calculating P(ALT) are poised to improve our current means of estimating DILI severity and the risk of acute liver failure. Springer International Publishing 2021-09-17 2021 /pmc/articles/PMC8447115/ /pubmed/34533782 http://dx.doi.org/10.1007/s40264-021-01109-4 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Clinton, Joseph William
Kiparizoska, Sara
Aggarwal, Soorya
Woo, Stephanie
Davis, William
Lewis, James H.
Drug-Induced Liver Injury: Highlights and Controversies in the Recent Literature
title Drug-Induced Liver Injury: Highlights and Controversies in the Recent Literature
title_full Drug-Induced Liver Injury: Highlights and Controversies in the Recent Literature
title_fullStr Drug-Induced Liver Injury: Highlights and Controversies in the Recent Literature
title_full_unstemmed Drug-Induced Liver Injury: Highlights and Controversies in the Recent Literature
title_short Drug-Induced Liver Injury: Highlights and Controversies in the Recent Literature
title_sort drug-induced liver injury: highlights and controversies in the recent literature
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447115/
https://www.ncbi.nlm.nih.gov/pubmed/34533782
http://dx.doi.org/10.1007/s40264-021-01109-4
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