药物遗传学,药物不良反应和公共卫生。

Regine Kollek, Jan van Aken, Gunter Feuerstein, Mechtild Schmedders
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引用次数: 22

摘要

药物不良反应(adr)是一个重大的公共卫生问题。药物治疗前的药物遗传学测试被认为可以大大缓解这个问题。通过系统的文献综述,辅以专家访谈,评估了药物遗传学的发展状况。对三个案例的分析表明,除了硫嘌呤甲基转移酶(TPMT)外,缺乏明确证明药物遗传学检测临床价值的研究。检测可以预防一些不良反应,但目前还不能预防所有不良反应。由于它不能弥补临床监测,药物遗传学可以被视为附加技术,应用于既定方法之外。在德国检验医学学会成员中进行的一项非代表性的探索性调查显示,对检测的需求是有限的,并且没有增加多少,尽管预计将来会有一定的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacogenetics, adverse drug reactions and public health.

Adverse drug reactions (ADRs) are a major public health problem. Pharmacogenetic testing prior to drug treatment is supposed to considerably alleviate this problem. The state of pharmacogenetic development was assessed by a systematic literature review, supplemented by expert interviews. Analysis of three case examples revealed that - with the exception of thiopurine methyltransferase (TPMT) - studies are lacking which unambiguously prove the clinical value of pharmacogenetic testing. Testing can prevent some, but by far not all ADRs. Since it does not compensate for clinical monitoring, pharmacogenetics can be regarded as add-on technology, applied in addition to established methods. A non-representative, explorative survey conducted amongst members of the German Society of Laboratory Medicine revealed that the demand for testing is limited and has not increased much, although a certain increase is expected in the future.

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