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Metabolic Comorbidities and Risk of Development and Severity of Drug-Induced Liver Injury

The incidence and rates of diagnosis of drug-induced liver injury (DILI) have been increasing in recent years as findings from basic research and the examination of clinical databases reveal information about the clinical course, etiology, and prognosis of this complex disease. The prevalence of met...

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Detalles Bibliográficos
Autores principales: Li, Xu, Gao, Pujun, Niu, Junqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720367/
https://www.ncbi.nlm.nih.gov/pubmed/31531370
http://dx.doi.org/10.1155/2019/8764093
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author Li, Xu
Gao, Pujun
Niu, Junqi
author_facet Li, Xu
Gao, Pujun
Niu, Junqi
author_sort Li, Xu
collection PubMed
description The incidence and rates of diagnosis of drug-induced liver injury (DILI) have been increasing in recent years as findings from basic research and the examination of clinical databases reveal information about the clinical course, etiology, and prognosis of this complex disease. The prevalence of metabolic comorbidities (e.g., diabetes mellitus, fatty liver, obesity, and metabolic syndrome (MetS)) has been increasing during the same period. The results of preclinical and clinical research studies indicate that characteristics of metabolic comorbidities are also factors that affect DILI phenotype and progression. The objective of this review is to present the evidence for DILI and hepatotoxicity mechanisms, incidence, and outcomes in patients with MetS and nonalcoholic fatty liver disease. Moreover, we also summarize the relationships between drugs used to treat metabolic comorbidities and DILI.
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spelling pubmed-67203672019-09-17 Metabolic Comorbidities and Risk of Development and Severity of Drug-Induced Liver Injury Li, Xu Gao, Pujun Niu, Junqi Biomed Res Int Review Article The incidence and rates of diagnosis of drug-induced liver injury (DILI) have been increasing in recent years as findings from basic research and the examination of clinical databases reveal information about the clinical course, etiology, and prognosis of this complex disease. The prevalence of metabolic comorbidities (e.g., diabetes mellitus, fatty liver, obesity, and metabolic syndrome (MetS)) has been increasing during the same period. The results of preclinical and clinical research studies indicate that characteristics of metabolic comorbidities are also factors that affect DILI phenotype and progression. The objective of this review is to present the evidence for DILI and hepatotoxicity mechanisms, incidence, and outcomes in patients with MetS and nonalcoholic fatty liver disease. Moreover, we also summarize the relationships between drugs used to treat metabolic comorbidities and DILI. Hindawi 2019-08-18 /pmc/articles/PMC6720367/ /pubmed/31531370 http://dx.doi.org/10.1155/2019/8764093 Text en Copyright © 2019 Xu Li et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Li, Xu
Gao, Pujun
Niu, Junqi
Metabolic Comorbidities and Risk of Development and Severity of Drug-Induced Liver Injury
title Metabolic Comorbidities and Risk of Development and Severity of Drug-Induced Liver Injury
title_full Metabolic Comorbidities and Risk of Development and Severity of Drug-Induced Liver Injury
title_fullStr Metabolic Comorbidities and Risk of Development and Severity of Drug-Induced Liver Injury
title_full_unstemmed Metabolic Comorbidities and Risk of Development and Severity of Drug-Induced Liver Injury
title_short Metabolic Comorbidities and Risk of Development and Severity of Drug-Induced Liver Injury
title_sort metabolic comorbidities and risk of development and severity of drug-induced liver injury
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720367/
https://www.ncbi.nlm.nih.gov/pubmed/31531370
http://dx.doi.org/10.1155/2019/8764093
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