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多基因风险评分用于识别 CVD 风险并制定个体化治疗方案:是希望还是炒作?

Polygenic Risk Scores to Identify CVD Risk and Tailor Therapy: Hope or Hype?

机构信息

Center for Prevention of Cardiovascular Disease, Section on Cardiovascular Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA.

出版信息

Curr Atheroscler Rep. 2021 Jun 28;23(9):47. doi: 10.1007/s11883-021-00950-3.

Abstract

PURPOSE OF REVIEW

The purpose of this review is to understand the conceptual basis and implications of polygenic risk scores (PRS) in assessing risk of future coronary artery disease (CAD).

RECENT FINDINGS

Genetic information from the USA and beyond has been pooled together to create population-based biobanks, composed of millions of genotyped individuals, which have helped further our understanding of the relationship between single nucleotide polymorphisms (SNPs) and CAD. Contemporary PRS composed of millions of SNPs now serve as the gold standard and have been evaluated in several cohort studies to predict risk of CAD and potentially help guide pharmacotherapy. The development of PRS has enhanced our understanding of the relationship between genes and disease, thereby facilitating CAD risk prediction. While certain constraints currently limit their utility in clinical practice, further refinement of this tool will enable clinicians to more fully understand genetic risk and improve preventive care.

摘要

目的综述

本文旨在了解多基因风险评分(PRS)在评估未来冠状动脉疾病(CAD)风险方面的概念基础和意义。

最近的发现

来自美国和其他地区的遗传信息已经被汇集在一起,创建了基于人群的生物库,其中包含数百万个基因分型个体,这有助于我们进一步了解单核苷酸多态性(SNP)与 CAD 之间的关系。由数百万个 SNP 组成的当代 PRS 现在是黄金标准,并已在多项队列研究中进行了评估,以预测 CAD 的风险,并可能有助于指导药物治疗。PRS 的发展增强了我们对基因与疾病之间关系的理解,从而有助于 CAD 风险预测。虽然目前某些限制限制了它们在临床实践中的应用,但进一步完善这一工具将使临床医生能够更全面地了解遗传风险并改善预防保健。

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