Ancestry-Matched and Cross-Ancestry Genetic Risk Scores of Type 2 Diabetes in Pregnant Women and Fetal Growth: A Study in an Ancestrally Diverse Cohort

被引:1
作者
Ouidir, Marion [1 ]
Zeng, Xuehuo [1 ]
Chatterjee, Suvo [1 ]
Zhang, Cuilin [1 ]
Tekola-Ayele, Fasil [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, NIH, Div Populat Hlth Res, Div Intramural Res,Epidemiol Branch, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
GENOME-WIDE ASSOCIATION; BIRTH-WEIGHT; INSULIN; GLUCOSE; SINGLETONS; ORIGINS; OBESITY; HEALTH;
D O I
10.2337/db21-0655
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Maternal genetic variants associated with offspring birth weight and adult type 2 diabetes (T2D) risk loci show some overlap. Whether T2D genetic risk influences longitudinal fetal weight and the gestational timing when these relationships begin is unknown. We investigated the associations of T2D genetic risk scores (GRS) with longitudinal fetal weight and birth weight among 1,513 pregnant women from four ancestral groups. Women had up to five ultrasonography examinations. Ancestry-matched GRS were constructed separately using 380 European- (GRSeur), 104 African- (GRSafr), and 189 East Asian- (GRSeas) related T2D loci discovered in different population groups. Among European Americans, the highest quartile GRSeur was significantly associated with 53.8 g higher fetal weight (95% CI 19.2-88.5) over the pregnancy. The associations began at gestational week 24 and continued through week 40, with a 106.8 g (95% CI 6.5-207.1) increase in birth weight. The findings were similar in analysis further adjusted for maternal glucose challenge test results. No consistent association was found using ancestry-matched or cross-ancestry GRS in non-Europeans. In conclusion, T2D genetic susceptibility may influence fetal growth starting at midsecond trimester among Europeans. Absence of similar associations in non-Europeans urges the need for further genetic T2D studies in diverse ancestries.
引用
收藏
页码:340 / 349
页数:10
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