人类白细胞抗原
遗传倾向
药品
遗传关联
等位基因
药物开发
肝损伤
候选基因
机制(生物学)
全基因组关联研究
生物信息学
医学
生物
基因
遗传学
单核苷酸多态性
基因型
药理学
哲学
认识论
抗原
作者
Camilla Stephens,M. Isabel Lucena,Raúl J. Andrade
标识
DOI:10.1080/17425255.2021.1854726
摘要
Introduction: Idiosyncratic drug-induced liver injury (DILI) is a challenging condition with widespread implications. The underlying mechanism of DILI is not yet fully elucidated, but genetic predispositions are believed to contribute to DILI susceptibility. The identification of genetic risk factors has been a goal in DILI research for more than two decades. Areas covered: Here we provide an overview of genetic studies in DILI performed to date and outline polymorphisms identified to have a potential role in DILI development. This review covers both earlier candidate gene studies and more recent genome-wide association studies. The clinical applications of these findings are also discussed. Expert opinion: Various polymorphisms have been identified as associated with DILI susceptibility, but all of these have not been confirmed in independent studies or contradictive findings are available. Genome-wide significant associations between distinct HLA risk alleles and DILI due to specific causative agents strengthen the hypothesis that DILI is partially immune-mediated. These HLA alleles generally have low positive predictive value and are therefore not useful in preemptive tests to reduce DILI incidences, but can aid DILI diagnosis and clinical decision-making.
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