Role of Genetic Polymorphisms in Drug-Induced Liver Injury (DILI)

A major cause of acute liver failure and drug reaction, drug induced liver injury (DILI) usually has a genetic component. This paper discusses the effect of genetic polymorphisms as a risk factor of DILI with reference to different inbred and genetically altered mouse models. Using the administration of hepatotoxic agent like acetaminophen, the study is used to compare the biochemical, morphologic, and gene expression in models among various strains. Data indicate that DBA/2 and Cyp2e1 knockout mice have a much higher liver enzymes and inflammatory gene expression response when compared to the resistant strains such as C57BL/6 and thus, strongly exhibits a genetic influence in DILI response. These inter-strain differences are confirmed as a result of statistical analyses such as ANOVA analysis, correlation and principal component analysis. The results reinforce the importance of genetic predisposition in drug safety and espouse the need to employ pharmacogenetic screening approaches within the preclinical studies as well as in clinical risk evaluation to enhance the efficacy of individualized medicine practices.

Authors

Institutions

Publication Details

Journal
Journal of Pharmacology Genetics and Molecular Biology
Published
2025-08-04
DOI
https://doi.org/10.64062/jpgmb.vol1.issue4.3
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Role of Genetic Polymorphisms in Drug-Induced Liver Injury (DILI)

Rajan Rajabalaya, Sheba R. David, Srikumar Chakravarthi, Mohammad Nazmul Hasan Maziz et al.
Journal of Pharmacology Genetics and Molecular Biology
Drug-Induced Hepatotoxicity and Protection
article

Role of Genetic Polymorphisms in Drug-Induced Liver Injury (DILI)

Rajan Rajabalaya, Sheba R. David, Srikumar Chakravarthi, Mohammad Nazmul Hasan Maziz, S Shanmugasundaram
article en

Abstract

A major cause of acute liver failure and drug reaction, drug induced liver injury (DILI) usually has a genetic component. This paper discusses the effect of genetic polymorphisms as a risk factor of DILI with reference to different inbred and genetically altered mouse models. Using the administration of hepatotoxic agent like acetaminophen, the study is used to compare the biochemical, morphologic, and gene expression in models among various strains. Data indicate that DBA/2 and Cyp2e1 knockout mice have a much higher liver enzymes and inflammatory gene expression response when compared to the resistant strains such as C57BL/6 and thus, strongly exhibits a genetic influence in DILI response. These inter-strain differences are confirmed as a result of statistical analyses such as ANOVA analysis, correlation and principal component analysis. The results reinforce the importance of genetic predisposition in drug safety and espouse the need to employ pharmacogenetic screening approaches within the preclinical studies as well as in clinical risk evaluation to enhance the efficacy of individualized medicine practices.

Journal of Pharmacology Genetics and Molecular Biology
University of Wyoming (US), Universiti Brunei Darussalam (BN), Umma University (KE), Perdana University (MY), Wyoming Department of Education (US), SEGi University (MY)
Openalex Percentile: Top 74%
Drug-Induced Hepatotoxicity and Protection
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Role of Genetic Polymorphisms in Drug-Induced Liver Injury (DILI) — Rajan Rajabalaya, Sheba R. David, et al. · Journal of Pharmacology Genetics and Molecular Biology (2025) | TGRS Research Map | TGRS