Takase Masato, Hozawa Atsushi
Graduate School of Medicine, Tohoku University.
Tohoku Medical Megabank Organization, Tohoku University.
J Atheroscler Thromb. 2025 Sep 1;32(9):1079-1097. doi: 10.5551/jat.RV22039. Epub 2025 Jul 4.
Polygenic risk scores (PRSs), constructed from numerous common single nucleotide polymorphisms (SNPs), have emerged as useful tools for predicting future atherosclerotic cardiovascular disease (ASCVD). PRSs have shown independent associations with ASCVD outcomes and are increasingly being considered to enhance risk stratification and guide primary prevention strategies. However, most evidence to date has been derived from populations of European ancestry, and their generalizability to other populations, including East Asians, remains uncertain. This review summarizes the current epidemiological evidence on the association between PRS and ASCVD outcomes, focusing on findings in Japanese cohorts. We discuss the potential of PRS as a clinical decision support tool, its incremental value over traditional risk factors, and its role in the early identification of high-risk individuals. We also highlight the limited number of prospective studies in the Japanese population, where validation and implementation studies are ongoing. Given the growing accessibility of genetic testing and the potential of PRS to complement conventional risk assessments, further large-scale studies are warranted to evaluate its clinical utility across diverse populations. Expanding ancestry-specific biobanks and improving PRS transferability are essential steps toward the equitable implementation of genomic risk prediction in ASCVD prevention.
多基因风险评分(PRSs)由众多常见单核苷酸多态性(SNPs)构建而成,已成为预测未来动脉粥样硬化性心血管疾病(ASCVD)的有用工具。PRSs已显示出与ASCVD结局的独立关联,并且越来越多地被认为可用于加强风险分层和指导一级预防策略。然而,迄今为止的大多数证据都来自欧洲血统人群,其在包括东亚人在内的其他人群中的可推广性仍不确定。本综述总结了目前关于PRS与ASCVD结局之间关联的流行病学证据,重点关注日本队列中的研究结果。我们讨论了PRS作为临床决策支持工具的潜力、其相对于传统风险因素的增量价值以及其在早期识别高危个体中的作用。我们还强调了日本人群中前瞻性研究数量有限,目前正在进行验证和实施研究。鉴于基因检测的可及性不断提高以及PRS补充传统风险评估的潜力,有必要开展进一步的大规模研究,以评估其在不同人群中的临床效用。扩大特定血统生物样本库并提高PRS的可转移性是在ASCVD预防中公平实施基因组风险预测的关键步骤。