Bray Michael J, Edwards Todd L, Wellons Melissa F, Jones Sarah H, Hartmann Katherine E, Velez Edwards Digna R
Vanderbilt Genetics Institute, Vanderbilt University, Nashville, Tennessee.
Vanderbilt Genetics Institute, Vanderbilt University, Nashville, Tennessee; Department of Medicine, Vanderbilt University, Nashville, Tennessee; Vanderbilt Epidemiology Center, Vanderbilt University, Nashville, Tennessee; Institute for Medicine and Public Health, Vanderbilt University, Nashville, Tennessee; Division of Epidemiology, Vanderbilt University, Nashville, Tennessee.
Fertil Steril. 2017 Dec;108(6):1034-1042.e26. doi: 10.1016/j.fertnstert.2017.09.018.
To evaluate the relationship between genetic ancestry and uterine fibroid characteristics.
Cross-sectional study.
Not applicable.
PATIENT(S): A total of 609 African American participants with image- or surgery-confirmed fibroids in a biorepository at Vanderbilt University electronic health record biorepository and the Coronary Artery Risk Development in Young Adults studies were included.
INTERVENTION(S): None.
MAIN OUTCOME MEASURE(S): Outcome measures include fibroid number (single vs. multiple), volume of largest fibroid, and largest fibroid dimension of all fibroid measurements.
RESULT(S): Global ancestry meta-analyses revealed a significant inverse association between percentage of European ancestry and risk of multiple fibroids (odds ratio: 0.78; 95% confidence interval 0.66, 0.93; P=6.05 × 10). Local ancestry meta-analyses revealed five suggestive (P<4.80 × 10) admixture mapping peaks in 2q14.3-2q21.1, 3p14.2-3p14.1, 7q32.2-7q33, 10q21.1, 14q24.2-14q24.3, for number of fibroids and one suggestive admixture mapping peak (P<1.97 × 10) in 10q24.1-10q24.32 for volume of largest fibroid. Single variant association meta-analyses of the strongest associated region from admixture mapping of fibroid number (10q21.1) revealed a strong association at single nucleotide polymorphism variant rs12219990 (odds ratio: 0.41; 95% confidence interval 0.28, 0.60; P=3.82 × 10) that was significant after correction for multiple testing.
CONCLUSION(S): Increasing African ancestry is associated with multiple fibroids but not with fibroid size. Local ancestry analyses identified several novel genomic regions not previously associated with fibroid number and increasing volume. Future studies are needed to explore the genetic impact that ancestry plays into the development of fibroid characteristics.
评估遗传血统与子宫肌瘤特征之间的关系。
横断面研究。
不适用。
共有609名非裔美国参与者,他们在范德比尔特大学电子健康记录生物样本库和青年成人冠状动脉风险发展研究中的生物样本库中患有经影像或手术确诊的肌瘤。
无。
观察指标包括肌瘤数量(单个与多个)、最大肌瘤体积以及所有肌瘤测量中的最大肌瘤尺寸。
全球血统荟萃分析显示,欧洲血统百分比与多发性肌瘤风险之间存在显著负相关(优势比:0.78;95%置信区间0.66,0.93;P = 6.05×10)。局部血统荟萃分析在2q14.3 - 2q21.1、3p14.2 - 3p14.1、7q32.2 - 7q33、10q21.1、14q24.2 - 14q24. 的肌瘤数量方面发现了五个提示性(P < 4.80×10)混合映射峰,在10q24.1 - 10q24.32的最大肌瘤体积方面发现了一个提示性混合映射峰(P < 1.97×10)。对肌瘤数量混合映射中最强关联区域(10q21.1)进行的单变体关联荟萃分析显示,在单核苷酸多态性变体rs12219990处存在强关联(优势比:0.41;95%置信区间0.28,0.60;P = 3.82×10),在进行多重检验校正后具有显著性。
非洲血统增加与多发性肌瘤相关,但与肌瘤大小无关。局部血统分析确定了几个以前与肌瘤数量和体积增加无关的新基因组区域。未来需要开展研究来探索血统对肌瘤特征发展的遗传影响。