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预测和预防急性药物性肝损伤:2010 年有哪些新进展?

Predicting and preventing acute drug-induced liver injury: what's new in 2010?

机构信息

Georgetown University Medical Center, 3800 Reservoir Road, NW, Washington, DC 20007, USA.

出版信息

Expert Opin Drug Metab Toxicol. 2010 Sep;6(9):1047-61. doi: 10.1517/17425255.2010.503706.

Abstract

IMPORTANCE OF THE FIELD

The field of drug-induced liver injury (DILI) continues to expand in terms of global registries and with new agents added every year. Given the need to improve on our current methods of preclinical testing and monitoring for DILI during both clinical trials and in the post-approval setting, there is increasing research aimed at better understanding why injury occurs and who is most susceptible. To this end, the active pursuit of biomarkers that will predict injury prior to its occurrence and genetic testing that can identify individuals at risk of DILI continue to be at the forefront.

AREAS COVERED IN THIS REVIEW

While alanine aminotransferase (ALT) testing remains the workhorse of biochemical monitoring, it only detects hepatic injury after it has occurred and, therefore, is not a true predictor. The utility and shortcomings of ALT and other liver tests are reviewed along with a synopsis of several other candidate biomarkers that are being studied. In addition, we review the recent data supporting testing for genetic predisposition to DILI and how identifying clinical risk factors may translate into better means for preventing DILI.

WHAT THE READER WILL GAIN

We update the basis on which age and gender are considered risk factors for DILI, and review the latest reports detailing the association of several candidate genes and the development of DILI in a susceptible patient. Human leukocyte antigen-B*5701 is closely linked to the hypersensitivity reaction seen with abacavir, and such screening has been successfully incorporated into HIV treatment around the globe and offers the promise that testing for other genetic markers will soon become a routine part of clinical practice. At present, candidate genes conferring specific susceptibility to DILI have been identified for a relatively few agents (e.g., flucloxacillin, amoxicillin-clavulanate, ximelagatran and isoniazid), but many more are under study. Preventing DILI often comes down to avoiding the use of potentially hepatotoxic drugs in certain situations, and we review the clinical scenarios in which this is most relevant.

TAKE HOME MESSAGE

Given the number and range of studies aimed at identifying predictors of DILI, the focus of this review is to summarize what we consider to be the most relevant new information published on the topics of clinical and genetic factors that predispose to DILI, the use of biomarkers as predictors of acute DILI, along with advances in prevention strategies.

摘要

重要性

药物性肝损伤(DILI)领域在全球注册方面不断扩大,每年都有新的药物加入。鉴于需要改进我们目前在临床试验期间和批准后进行 DILI 的临床前测试和监测方法,因此越来越多的研究旨在更好地了解为什么会发生损伤以及谁最容易受到影响。为此,积极寻求可在损伤发生之前预测损伤的生物标志物以及可识别 DILI 风险个体的基因检测继续处于前沿。

涵盖的领域

虽然丙氨酸氨基转移酶(ALT)检测仍然是生化监测的主力,但它仅在发生肝损伤后才检测到,因此不是真正的预测指标。本文回顾了 ALT 和其他肝脏检测的用途和缺点,并简述了正在研究的其他几种候选生物标志物。此外,我们还回顾了支持检测 DILI 遗传易感性的最新数据,以及如何将识别临床风险因素转化为更好的预防 DILI 的方法。

读者将获得什么

我们更新了年龄和性别被视为 DILI 危险因素的依据,并回顾了最新报告,详细说明了几种候选基因与易感患者 DILI 发展的关联。人类白细胞抗原-B*5701 与阿巴卡韦引起的超敏反应密切相关,这种筛查已成功纳入全球 HIV 治疗中,并有望在不久的将来,检测其他遗传标志物将成为临床实践的常规部分。目前,已经确定了少数药物(例如氟氯西林、阿莫西林克拉维酸、西米拉坦和异烟肼)具有特定的 DILI 易感性的候选基因,但更多的基因正在研究中。预防 DILI 通常归结为在某些情况下避免使用潜在的肝毒性药物,我们回顾了最相关的临床情况。

一句话总结

鉴于为数众多且范围广泛的旨在确定 DILI 预测因子的研究,本综述的重点是总结我们认为与易患 DILI 的临床和遗传因素、生物标志物作为急性 DILI 预测因子的用途以及预防策略方面的最新相关信息。

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