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族群的重要性:多基因乳腺癌风险评分是否适用于非白种欧洲血统的女性?

The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?

机构信息

Nightingale/Prevent Breast Cancer Centre, Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK.

Manchester Breast Centre, Manchester Cancer Research Centre, The Christie Hospital, Manchester, UK.

出版信息

Int J Cancer. 2022 Jan 1;150(1):73-79. doi: 10.1002/ijc.33782. Epub 2021 Sep 7.

DOI:10.1002/ijc.33782
PMID:34460111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9290473/
Abstract

Polygenic risk scores (PRS) for disease risk stratification show great promise for application in general populations, but most are based on data from individuals of White European origin. We assessed two well validated PRS (SNP18, SNP143) in the Predicting-Risk-of-Cancer-At-Screening (PROCAS) study in North-West England for breast cancer prediction based on ethnicity. Overall, 9475 women without breast cancer at study entry, including 645 who subsequently developed invasive breast cancer or ductal carcinoma in situ provided DNA. All were genotyped for SNP18 and a subset of 1868 controls were genotyped for SNP143. For White Europeans both PRS discriminated well between individuals with and without cancer. For n = 395 Black (n = 112), Asian (n = 119), mixed (n = 44) or Jewish (n = 120) women without cancer both PRS overestimated breast cancer risk, being most marked for women of Black and Jewish origin (P < .001). SNP143 resulted in a potential mean 40% breast cancer risk overestimation in the combined group of non-White/non-European origin. SNP-PRS that has been normalized based on White European ethnicity for breast cancer should not be used to predict risk in women of other ethnicities. There is an urgent need to develop PRS specific for other ethnicities, in order to widen access of this technology.

摘要

多基因风险评分(PRS)在疾病风险分层方面显示出巨大的应用前景,但大多数 PRS 都是基于白种欧洲人群的数据。我们在英格兰西北部的预测癌症筛查风险(PROCAS)研究中评估了两种经过充分验证的 PRS(SNP18、SNP143),以评估其在种族基础上对乳腺癌的预测能力。共有 9475 名在研究开始时没有乳腺癌的女性(包括 645 名随后发生浸润性乳腺癌或导管原位癌的女性)提供了 DNA。所有女性均进行了 SNP18 基因分型,1868 名对照组中的一部分女性进行了 SNP143 基因分型。对于白种欧洲人,两种 PRS 都能很好地区分有癌症和无癌症的个体。对于 395 名黑人(n=112)、亚洲人(n=119)、混血儿(n=44)或犹太人(n=120)无癌症的女性,两种 PRS 都高估了乳腺癌风险,黑人和犹太裔女性的风险高估最为明显(P<0.001)。在非白种/非欧洲血统的女性中,SNP143 导致潜在的平均 40%的乳腺癌风险高估。基于白种欧洲种族进行乳腺癌校正的 SNP-PRS 不应用于预测其他种族女性的风险。迫切需要开发针对其他种族的 PRS,以扩大这项技术的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0435/9290473/ad2380f5df6e/IJC-150-73-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0435/9290473/ad2380f5df6e/IJC-150-73-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0435/9290473/ad2380f5df6e/IJC-150-73-g001.jpg

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