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Ancillary risk information and pharmacogenetic tests: social and policy implications.

机译:辅助风险信息和药物遗传学检测:对社会和政策的影响。

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摘要

Some pharmacogenetic tests may provide ancillary disease risk information. To evaluate evidence and assess the social and policy implications of ancillary disease risk information associated with candidate pharmacogenetic variants, We conducted a literature search and abstract review of disease susceptibility studies for each of 42 gene variants potentially associated with drug response. Twenty-two variants (53%) had suggested association with disease risk in at least two studies, and sixteen (38%) were for diseases other than the pharmacogenetic indication. Seven variants (16%) were associated with risk for at least two different diseases. Pharmacogenetic tests have the potential to provide ancillary disease risk information, and this potential should be considered as pharmacogenetic tests are brought into clinical use. Implications will vary with each test but tests should be evaluated individually within a framework that outlines the potential implications of ancillary information.
机译:一些药物遗传学检测可能会提供辅助疾病风险信息。为了评估证据并评估与候选药物遗传学变异相关的辅助疾病风险信息的社会和政策意义,我们针对可能与药物反应相关的42个基因变异中的每一个,进行了文献检索和对疾病敏感性研究的抽象综述。在至少两项研究中,有22种变体(53%)提示与疾病风险相关,而有16种(38%)与药物遗传学适应症以外的疾病有关。七个变异(16%)与至少两种不同疾病的风险相关。药物遗传学测试具有提供辅助疾病风险信息的潜力,并且当将药物遗传学测试投入临床使用时,应考虑这种潜力。每种测试的含义会有所不同,但应在概述辅助信息潜在含义的框架内对测试进行单独评估。

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