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联合磁共振成像与多血统多基因风险评分以提高临床显著前列腺癌的识别能力。

Combining magnetic resonance imaging with a multi-ancestry polygenic risk score to improve identification of clinically significant prostate cancer.

机构信息

Department of Urology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

出版信息

JNCI Cancer Spectr. 2024 Feb 29;8(2). doi: 10.1093/jncics/pkae014.

Abstract

Multi-parametric magnetic resonance imaging (mpMRI) has emerged as an important tool for identifying clinically significant prostate cancer. We examined if the addition of a 400-variant multi-ancestry polygenic risk score (PRS) to mpMRI has the potential to improve identification. Based on data from 24 617 men from the Mass General Brigham Biobank, we identified 1243 men who underwent mpMRI. Men in the top PRS quartile were more likely to have clinically significant prostate cancer (47.1% vs 28.6% in the bottom PRS quartile, adjusted relative proportion 1.72 [95% CI = 1.35 to 2.19]). Both among men with a positive and a negative mpMRI, men in the top PRS quartile had the highest frequency of clinically significant cancer. In a constructed scenario for selecting men to undergo biopsy, use of the PRS lowered the frequency of missed clinically significant cancers from 9.1% to 5.9%. Our study provides initial support for using the PRS to improve identification of potentially lethal prostate cancer.

摘要

多参数磁共振成像(mpMRI)已成为识别临床显著前列腺癌的重要工具。我们研究了增加一个包含 400 个变体的多祖源多基因风险评分(PRS)是否有可能提高识别能力。基于来自麻省总医院布列根生物库的 24617 名男性的数据,我们确定了 1243 名接受 mpMRI 的男性。PRS 最高四分位数的男性更有可能患有临床显著的前列腺癌(47.1% vs 最低四分位数的 28.6%,调整后的相对比例为 1.72[95%CI=1.35 至 2.19])。无论是在 mpMRI 阳性还是阴性的男性中,PRS 最高四分位数的男性具有最高的临床显著癌症频率。在构建的选择接受活检的男性的情景中,使用 PRS 将漏诊的临床显著癌症的频率从 9.1%降低至 5.9%。我们的研究初步支持使用 PRS 来提高潜在致命性前列腺癌的识别能力。

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Genetic predisposition to prostate cancer: an update.遗传性前列腺癌易感性:最新研究进展。
Fam Cancer. 2022 Jan;21(1):101-114. doi: 10.1007/s10689-021-00227-3. Epub 2021 Jan 24.

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