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Genetic association studies in drug-induced liver injury.

机译:药物性肝损伤的遗传关联研究。

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摘要

Genetic studies on drug-induced liver injury (DILI) have proved challenging, both because of their rarity and their difficulty in replicating observed effects. However, significant progress has now been achieved by both candidate-gene and genome-wide association studies. These two approaches are considered in detail, together with examples of DILI due to specific drugs where consistent associations have been reported. Particular consideration is given to associations between antituberculosis drug-related liver injury and the "slow acetylator" genotype for N-acetyltransferase 2, amoxicillin/clavulanate-related liver injury, and the human leukocyte antigen (HLA) class II DRB1*1501 allele and flucloxacillin-related injury and the HLA class I B*5701 allele. Although these associations are drug-specific, the possibility that additional, more general susceptibility genes for DILI exist requires further investigation, ideally by genome-wide association studies involving international collaboration. The possibility of interethnic variation in susceptibility to DILI also requires further study.
机译:药物诱发的肝损伤(DILI)的遗传研究已被证明具有挑战性,这既因为其罕见性又难以复制观察到的效应。然而,候选基因和全基因组关联研究现已取得重大进展。详细介绍了这两种方法,以及由于已报道了一致关联的特定药物导致的DILI实例。特别考虑到抗结核药物相关的肝损伤与N-乙酰基转移酶2的“慢乙酰化剂”基因型,阿莫西林/克拉维酸相关的肝损伤和人类白细胞抗原(HLA)II类DRB1 * 1501等位基因和氟氯西林之间的关联相关损伤和HLA IB * 5701类等位基因。尽管这些关联是药物特异性的,但存在更多,更普遍的DILI易感基因的可能性需要进一步研究,最好是通过涉及国际合作的全基因组关联研究。民族间对DILI易感性变化的可能性也需要进一步研究。

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