Ma Chaoran, Ericsson Caroline, Carlsson Sigrid V, Lilja Hans, Kibel Adam, Graff Rebecca E, Plym Anna, Giovannucci Edward, Mucci Lorelei A, Preston Mark A, Penney Kathryn L
Channing Division of Network Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Eur Urol Open Sci. 2023 Feb 18;50:27-30. doi: 10.1016/j.euros.2023.01.012. eCollection 2023 Apr.
Men with a low prostate-specific antigen (PSA) level (<1 ng/ml) in midlife may extend the rescreening interval (if aged 40-59 yr) or forgo future PSA screening (if aged >60 yr) owing to their low risk of aggressive prostate cancer (PCa). However, there is a subset of men who develop lethal PCa despite low baseline PSA. We investigated how a PCa polygenic risk score (PRS) in addition to baseline PSA impacts the prediction of lethal PCa among 483 men aged 40-70 yr from the Physicians' Health Study followed over a median of 33 yr. We examined the association of the PRS with the risk of lethal PCa (lethal cases vs controls) using logistic regression adjusted for baseline PSA. The PCa PRS was associated with risk of lethal PCa (odds ratio per 1 standard deviation in PRS [OR] 1.79, 95% confidence interval [CI] 1.28-2.49). The association between the PRS and lethal PCa was stronger for those with PSA <1 ng/ml (OR 2.23, 95% CI 1.19-4.21) than for men with PSA ≥1 ng/ml (OR 1.61, 95% CI 1.07-2.42). Our PCa PRS improved the identification of men with PSA <1 ng/ml at greater risk of future lethal PCa who should consider ongoing PSA testing.
A subset of men develop fatal prostate cancer despite having low prostate-specific antigen (PSA) levels in middle age. A risk score based on multiple genes can help in predicting men who may be at risk of developing lethal prostate cancer and who should be advised to have regular PSA measurements.
中年时前列腺特异性抗原(PSA)水平较低(<1 ng/ml)的男性,由于其患侵袭性前列腺癌(PCa)的风险较低,可能会延长复查间隔时间(如果年龄在40 - 59岁)或放弃未来的PSA筛查(如果年龄>60岁)。然而,有一部分男性尽管基线PSA较低,但仍会发展为致命性PCa。我们研究了除基线PSA外,PCa多基因风险评分(PRS)如何影响来自医师健康研究的483名年龄在40 - 70岁、随访中位时间为33年的男性中致命性PCa的预测。我们使用经基线PSA调整的逻辑回归分析了PRS与致命性PCa风险(致命病例与对照)之间的关联。PCa PRS与致命性PCa风险相关(PRS每增加1个标准差的比值比[OR]为1.79,95%置信区间[CI]为1.28 - 2.49)。对于PSA<1 ng/ml的男性,PRS与致命性PCa之间的关联更强(OR为2.23,95% CI为1.19 - 4.21),而对于PSA≥1 ng/ml的男性,关联较弱(OR为1.61,95% CI为1.07 - 2.42)。我们的PCa PRS改进了对PSA<1 ng/ml且未来发生致命性PCa风险较高的男性的识别,这些男性应考虑持续进行PSA检测。
一部分男性尽管中年时前列腺特异性抗原(PSA)水平较低,但仍会发展为致命性前列腺癌。基于多个基因的风险评分有助于预测可能有发展为致命性前列腺癌风险的男性,以及应建议其定期进行PSA检测的男性。