Coignet Marie V, Zirpoli Gary Robert, Roberts Michelle R, Khoury Thaer, Bandera Elisa V, Zhu Qianqian, Yao Song
Department of Cancer Prevention and Control, Roswell Park Cancer Institute, Buffalo, NY, United States of America.
Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States of America.
PLoS One. 2017 Oct 26;12(10):e0187205. doi: 10.1371/journal.pone.0187205. eCollection 2017.
Reproductive aging phenotypes, including age at menarche (AM) and age at natural menopause (ANM), are well-established risk factors for breast cancer. In recent years, many genetic variants have been identified in association with AM and ANM in genome-wide association studies among European populations. Using data from the Women's Circle of Health Study (WCHS) of 1,307 European-American (EA) and 1,365 African-American (AA) breast cancer cases and controls, we aimed to replicate 53 earlier GWAS variants for AM and ANM in AA and EA groups and to perform analyses on total and net reproductive lifespan (TRLS; NRLS). Breast cancer risk was also examined in relation to a polygenic risk score (PRS) for each of the reproductive aging phenotypes. We replicated a number of variants in EA women, including rs7759938 in LIN28B for AM and rs16991615 in MCM8 for ANM; whereas in the AA group, only one SNP (rs2947411 in TMEM18) for AM was directionally consistent and nominally significant. In analysis of TRLS and NRLS, several SNPs were significant, including rs466639 in RXRG that was associated with both phenotypes in both AA and EA groups. None of the PRS was associated with breast cancer risk. Given the paucity of data available among AA populations, our study contributes to the literature of genetics of reproductive aging in AA women and highlights the importance of cross population replication of GWAS variants.
生殖衰老表型,包括初潮年龄(AM)和自然绝经年龄(ANM),是乳腺癌公认的风险因素。近年来,在欧洲人群的全基因组关联研究中,已鉴定出许多与AM和ANM相关的基因变异。利用来自健康女性圈研究(WCHS)的1307名欧美(EA)和1365名非裔美国(AA)乳腺癌病例及对照的数据,我们旨在在AA和EA组中复制53个先前针对AM和ANM的全基因组关联研究(GWAS)变异,并对总生殖寿命和净生殖寿命(TRLS;NRLS)进行分析。还针对每种生殖衰老表型的多基因风险评分(PRS)检查了乳腺癌风险。我们在EA女性中复制了多个变异,包括LIN28B基因中的rs7759938与AM相关,MCM8基因中的rs16991615与ANM相关;而在AA组中,只有一个与AM相关的单核苷酸多态性(TMEM18基因中的rs2947411)在方向上一致且具有名义上的显著性。在TRLS和NRLS分析中,有几个单核苷酸多态性是显著的,包括RXRG基因中的rs466639,它在AA和EA组中均与两种表型相关。没有一个PRS与乳腺癌风险相关。鉴于AA人群中可用数据的匮乏,我们的研究为AA女性生殖衰老遗传学文献做出了贡献,并强调了GWAS变异跨人群复制的重要性。