Department of Bioinformatics and Biostatistics, School of Life Science and Technology, Shanghai Jiao Tong University, Shanghai, China.
Department of Nutritional Sciences, University of Michigan School of Public Health, Ann Arbor, MI, USA.
J Hum Genet. 2022 Jun;67(6):331-338. doi: 10.1038/s10038-022-01010-7. Epub 2022 Jan 12.
Prevalence of obesity, type 2 diabetes (T2D), and being born with low birth weight are much higher in African American women compared to U.S. white women. Genetic factors may contribute to the excess risk of these conditions. We conducted admixture mapping of body mass index (BMI) at age 18, adult BMI, and adult waist circumference and waist-to-hip ratio adjusted for BMI using 2918 ancestral informative markers in 2596 participants of the Black Women's Health Study. We also searched for evidence of shared African genetic ancestry components among the four examined anthropometric traits and among birth weight and T2D. We found that global percent African ancestry was associated with higher adult BMI. We also found that African ancestry at 9q34 was associated with lower BMI at age 18. Our shared ancestry analysis identified ten genomic regions with local African ancestry associated with multiple traits. Seven out of these ten genomic loci were related to T2D risk. Of special interest is the 12q14-21 region where local African ancestry was associated with low birth weight, low BMI, high BMI-adjusted waist-to-hip ratio, and high T2D risk. Findings in the 12q14-21 genomic locus are consistent with the fetal insulin hypothesis that postulates that low birth weight and T2D have a common genetic basis, and they support the hypothesis of a shared African genetic ancestry component linking low birth weight and T2D in African Americans. Future studies should identify the actual genetic variants responsible for the clustering of these conditions in African Americans.
与美国白人女性相比,非裔美国女性的肥胖症、2 型糖尿病(T2D)和低出生体重的患病率要高得多。遗传因素可能导致这些疾病的风险增加。我们使用 2596 名黑人妇女健康研究参与者的 2918 个祖先信息标记,对 18 岁时的体重指数(BMI)、成年 BMI 和成年腰围以及调整 BMI 的腰围与臀围比进行了混合映射。我们还搜索了四个被检查的人体测量特征以及出生体重和 T2D 之间的非洲遗传祖先成分的共享证据。我们发现,全球非洲血统百分比与成年 BMI 较高有关。我们还发现,9q34 处的非洲血统与 18 岁时的 BMI 较低有关。我们的共享祖先分析确定了十个与多个特征相关的具有局部非洲祖先的基因组区域。这十个基因组位点中的七个与 T2D 风险有关。特别值得注意的是 12q14-21 区域,其中局部非洲血统与低出生体重、低 BMI、高 BMI 调整后的腰围与臀围比和高 T2D 风险有关。12q14-21 基因组位置的发现与胎儿胰岛素假说一致,该假说认为低出生体重和 T2D 具有共同的遗传基础,并支持低出生体重和 T2D 在非裔美国人中具有共同的非洲遗传祖先成分的假说。未来的研究应该确定导致这些非裔美国人的这些疾病聚集的实际遗传变异。