心血管精准医学——药物基因组学视角

Cambridge prisms, Precision medicine Pub Date : 2023-06-29 eCollection Date: 2023-01-01 DOI:10.1017/pcm.2023.17
Sandosh Padmanabhan, Clea du Toit, Anna F Dominiczak
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引用次数: 0

摘要

精准医学设想将个人的临床和生物学特征从实验室测试、成像、高通量组学和健康记录中整合起来,以推动个性化的诊断和治疗方法,提高成功率。根据目前的一刀切治疗策略,只有多达一半的患者对处方药物有反应,因此显然需要一种更加个性化的方法。通过精准医疗改变医疗保健的途径之一是药物基因组学(PGx)。据估计,约95%的人口携带一种或多种可操作的药物遗传变异,超过75%的50岁以上的成年人正在服用已知与PGx相关的处方。虽然在临床实践中有令人信服的药物基因组学实施的例子,但心血管PGx的情况仍在发展。在这篇综述中,我们将总结PGx在心血管疾病中的现状,并着眼于PGx在临床实践中实施的关键推动因素和障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiovascular precision medicine - A pharmacogenomic perspective.

Precision medicine envisages the integration of an individual's clinical and biological features obtained from laboratory tests, imaging, high-throughput omics and health records, to drive a personalised approach to diagnosis and treatment with a higher chance of success. As only up to half of patients respond to medication prescribed following the current one-size-fits-all treatment strategy, the need for a more personalised approach is evident. One of the routes to transforming healthcare through precision medicine is pharmacogenomics (PGx). Around 95% of the population is estimated to carry one or more actionable pharmacogenetic variants and over 75% of adults over 50 years old are on a prescription with a known PGx association. Whilst there are compelling examples of pharmacogenomic implementation in clinical practice, the case for cardiovascular PGx is still evolving. In this review, we shall summarise the current status of PGx in cardiovascular diseases and look at the key enablers and barriers to PGx implementation in clinical practice.

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