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Review
. 2019 Aug 18:2019:8764093.
doi: 10.1155/2019/8764093. eCollection 2019.

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

Affiliations
Review

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

Xu Li et al. Biomed Res Int. .

Abstract

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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Conflict of interest statement

The authors declare that there are no conflicts of interest associated with the publication of this manuscript.

References

    1. Han D., Shinohara M., Ybanez M. D., Saberi B., Kaplowitz N. Handbook of Experimental Pharmacology. 2010. Signal transduction pathways involved in drug-induced liver injury; pp. 267–310. - PubMed
    1. Krauskopf J., Caiment F., Claessen S. M., et al. Application of high-throughput sequencing to circulating microRNAs reveals novel biomarkers for drug-induced liver injury. Toxicological Sciences. 2015;143(2):268–276. doi: 10.1093/toxsci/kfu232. - DOI - PubMed
    1. Hunt C. M., Papay J. I., Stanulovic V., Regev A. Drug rechallenge following drug-induced liver injury. Hepatology. 2017;66:646–654. doi: 10.1002/hep.29152. - DOI - PubMed
    1. Stirnimann G., Kessebohm K., Lauterburg B. Liver injury caused by drugs: an update. Swiss Medical Weekly. 2010;140 doi: 10.4414/smw.2010.13080.13080 - DOI - PubMed
    1. Lee S. J., Lee Y. J., Park K. K. The pathogenesis of drug-induced liver injury. Expert Review of Gastroenterology & Hepatology. 2016:1175–1185. doi: 10.1080/17474124.2016.1196133. - DOI - PubMed