Slone Epidemiology Center at Boston University, 1010 Commonwealth Avenue, 4th Floor, Boston, MA 02215, USA.
Am J Epidemiol. 2012 Dec 15;176(12):1159-68. doi: 10.1093/aje/kws276. Epub 2012 Nov 15.
Rates of uterine leiomyomata (UL) are 2-3 times higher in African Americans than in European Americans. It is unclear whether inherited factors explain the ethnic disparity. To investigate the presence of risk alleles for UL that are highly differentiated in frequency between African Americans and European Americans, the authors conducted an admixture-based genome-wide scan of 2,453 UL cases confirmed by ultrasound or surgery in the Black Women's Health Study (1997-2009), a national prospective cohort study. Controls (n = 2,102) were women who did not report a UL diagnosis through 2009. Mean percentage of European ancestry was significantly lower among cases (20.00%) than among controls (21.63%; age-adjusted mean difference = -1.76%, 95% confidence interval: -2.40, -1.12; P < 0.0001), and the association was stronger in younger cases. Admixture analyses showed suggestive evidence of association at chromosomes 2, 4, and 10. The authors also genotyped a dense set of tag single nucleotide polymorphisms at different loci associated with UL in Japanese women but failed to replicate the associations. This suggests that genetic variation for UL differs in populations with and without African ancestry. The admixture findings further indicate that no single highly differentiated locus is responsible for the ethnic disparity in UL, raising the possibility that multiple variants jointly contribute to the higher incidence of UL in African Americans.
非裔美国人的子宫肌瘤(UL)发病率比欧洲裔美国人高 2-3 倍。目前尚不清楚遗传因素是否可以解释这种种族差异。为了研究在 UL 中存在风险等位基因,这些等位基因在非洲裔美国人和欧洲裔美国人之间的频率存在高度差异,作者对 2453 例经超声或手术证实的 UL 病例(1997-2009 年)进行了基于混合的全基因组扫描,这些病例来自黑人女性健康研究(Black Women's Health Study),这是一项全国性的前瞻性队列研究。对照组(n=2102)为截至 2009 年未报告 UL 诊断的女性。病例组中欧洲血统的平均百分比明显低于对照组(20.00%比 21.63%;年龄调整后的平均差异=-1.76%,95%置信区间:-2.40,-1.12;P<0.0001),且该关联在年轻病例中更强。混合分析显示,2、4 和 10 号染色体上存在关联的提示性证据。作者还对在日本女性中与 UL 相关的不同位点的一组高密度标签单核苷酸多态性进行了基因分型,但未能复制这些关联。这表明,具有和不具有非洲血统的人群中,UL 的遗传变异是不同的。混合分析的结果进一步表明,没有一个单一的高度分化的位点可以解释 UL 中的种族差异,这增加了多种变异共同导致非洲裔美国人 UL 发病率较高的可能性。