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非裔美国人和欧洲裔美国女性的纤维瘤特征的跨种族和种族分层全基因组关联研究。

Transethnic and race-stratified genome-wide association study of fibroid characteristics in African American and European American women.

机构信息

Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, Tennessee.

Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

出版信息

Fertil Steril. 2018 Sep;110(4):737-745.e34. doi: 10.1016/j.fertnstert.2018.04.035.

DOI:10.1016/j.fertnstert.2018.04.035
PMID:30196971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6132266/
Abstract

OBJECTIVE

To identify, through genome-wide association studies, genetic loci that associate with differences in fibroid size and number in a population of African American and European American women.

DESIGN

Cross-sectional study.

SETTING

Not applicable.

PATIENT(S): Using BioVU, a clinical population from the Vanderbilt University Medical Center, and the Coronary Artery Risk Development in Young Adults cohort, a prospective cohort, we identified 1520 women (609 African American and 911 European American) with documented fibroid characteristics.

INTERVENTION(S): None.

MAIN OUTCOME MEASURE(S): Outcome measurements include volume of largest fibroid, largest fibroid dimension, and number of fibroids (single vs. multiple).

RESULT(S): In race-stratified analyses we achieved genome-wide significance at a variant located between MAT2B and TENM2 (rs57542984, β = 0.13; 95% confidence interval 0.09, 0.17) for analyses of largest fibroid dimension in African Americans. The strongest signal for transethnic analyses was at a variant on 1q31.1 located between PLA2G4A and BRINP3 (rs6605005, β = 0.24; 95% confidence interval 0.15, 0.33) for fibroid volume. Results from MetaXcan identified an association between predicted expression of the gene ER degradation enhancing alpha-mannosidase like protein 2 (EDEM2) in the thyroid and number of fibroids (Z score = -4.51).

CONCLUSION(S): This study identified many novel associations between genetic loci and fibroid size and number in both race-stratified and transethnic analyses. Future studies are necessary to further validate our study findings and to better understand the mechanisms underlying these associations.

摘要

目的

通过全基因组关联研究,确定与非裔美国人和欧洲裔美国女性人群中子宫肌瘤大小和数量差异相关的遗传位点。

设计

横断面研究。

环境

不适用。

患者

利用范德比尔特大学医学中心的临床人群 BioVU 和前瞻性队列研究的冠状动脉风险发展在年轻人中,我们确定了 1520 名有记录的子宫肌瘤特征的女性(609 名非裔美国人和 911 名欧洲裔美国人)。

干预措施

无。

主要观察指标

包括最大肌瘤体积、最大肌瘤尺寸和肌瘤数量(单发与多发)的测量结果。

结果

在按种族分层的分析中,我们在位于 MAT2B 和 TENM2 之间的变异体(rs57542984,β=0.13;95%置信区间 0.09,0.17)处达到了全基因组显著性,用于分析非裔美国人的最大肌瘤尺寸。跨种族分析最强的信号位于位于 PLA2G4A 和 BRINP3 之间的 1q31.1 上的变异体(rs6605005,β=0.24;95%置信区间 0.15,0.33),用于分析肌瘤体积。MetaXcan 的结果确定了甲状腺中 EDEM2 基因预测表达与肌瘤数量之间的关联(Z 评分=-4.51)。

结论

本研究在种族分层和跨种族分析中确定了许多遗传位点与子宫肌瘤大小和数量之间的新关联。未来的研究有必要进一步验证我们的研究结果,并更好地理解这些关联的潜在机制。

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