多基因风险评分的临床实用性:2023年的关键评估。

IF 1.5 Q4 GENETICS & HEREDITY Journal of Community Genetics Pub Date : 2023-10-01 Epub Date: 2023-05-03 DOI:10.1007/s12687-023-00645-z
Sebastian Koch, Jörg Schmidtke, Michael Krawczak, Amke Caliebe
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引用次数: 4

摘要

自2009年首次出现在精神分裂症和双相情感障碍的背景下以来,多基因风险评分(PRS)已被描述用于大量常见的复杂疾病。然而,PRS在疾病风险评估或治疗决策中的临床应用可能是有限的,因为PRS通常只考虑一种特征的可遗传成分,而忽略了环境和生活方式的病因作用。我们调查了各种疾病的PRS的现状,包括乳腺癌症、糖尿病、癌症、冠状动脉疾病和帕金森病,并特别关注它们与PRS结合对临床评分的潜在改善。我们观察到,正如预期的那样,单独使用PRS的诊断和预后表现一直很低。此外,将PRS与临床评分相结合,充其量可以适度改善任一风险标志物的功效。尽管科学文献中报道了大量PRS,但对其临床效用的前瞻性研究,特别是与PRS相关的标准筛查或治疗程序的改进,仍然很少。总之,基于PRS的现有诊断或治疗方案的扩展对个体患者或整个医疗保健系统的益处仍然难以判断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Clinical utility of polygenic risk scores: a critical 2023 appraisal.

Since their first appearance in the context of schizophrenia and bipolar disorder in 2009, polygenic risk scores (PRSs) have been described for a large number of common complex diseases. However, the clinical utility of PRSs in disease risk assessment or therapeutic decision making is likely limited because PRSs usually only account for the heritable component of a trait and ignore the etiological role of environment and lifestyle. We surveyed the current state of PRSs for various diseases, including breast cancer, diabetes, prostate cancer, coronary artery disease, and Parkinson disease, with an extra focus upon the potential improvement of clinical scores by their combination with PRSs. We observed that the diagnostic and prognostic performance of PRSs alone is consistently low, as expected. Moreover, combining a PRS with a clinical score at best led to moderate improvement of the power of either risk marker. Despite the large number of PRSs reported in the scientific literature, prospective studies of their clinical utility, particularly of the PRS-associated improvement of standard screening or therapeutic procedures, are still rare. In conclusion, the benefit to individual patients or the health care system in general of PRS-based extensions of existing diagnostic or treatment regimens is still difficult to judge.

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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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