GLP-1R Polymorphisms Modify the Relationship Between Exposure to Gestational Diabetes Mellitus and Offspring BMI Growth: The EPOCH Study.

IF 16.6
Diabetes care Pub Date : 2025-07-01 DOI:10.2337/dc25-0194
Kylie K Harrall, Deborah H Glueck, Leslie A Lange, Elizabeth M Litkowski, Lauren A Vanderlinden, Iain R Konigsberg, Melanie G Cree, Wei Perng, Dana Dabelea
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Abstract

Objective: Exposure to maternal gestational diabetes mellitus (GDM) is associated with childhood BMI. Among youth, we explored whether three different glucagon-like peptide 1 receptor gene (GLP-1R) polymorphisms modified the associations between 1) GDM and BMI trajectories and 2) GDM and markers of glucose-insulin homeostasis.

Research design and methods: For 464 participants from the Exploring Perinatal Outcomes Among Children (EPOCH) study, microarray genotyping was performed during childhood (∼10 years). BMI trajectories across childhood and adolescence were characterized using repeated measurements from research visits and medical record abstraction. Markers of glucose-insulin homeostasis were derived from one oral glucose tolerance test in adolescence (∼16 years). Linear models assessed effect modification by GLP-1R polymorphisms.

Results: Among youth with at least one minor allele of rs10305420 (CT or TT) or rs1042044 (CA or AA), but not among major allele homozygotes, exposure to GDM was associated with higher average BMI. For rs6923761, participants who were exposed to GDM and were major allele homozygotes (i.e., genotype GG) had significantly higher average BMI than all other participants in the cohort. No polymorphisms modified the association between GDM and markers of glucose-insulin homeostasis during adolescence.

Conclusions: GLP-1R polymorphisms modify the association between GDM and BMI growth among youth. Further studies are needed to replicate these findings, and to better understand the mechanisms by which GLP-1R polymorphisms lead to heterogeneity in offspring BMI growth.

GLP-1R多态性改变妊娠期糖尿病暴露与后代BMI增长之间的关系:EPOCH研究
目的:暴露于母体妊娠期糖尿病(GDM)与儿童BMI相关。在年轻人中,我们探讨了三种不同的胰高血糖素样肽1受体基因(GLP-1R)多态性是否改变了1)GDM与BMI轨迹和2)GDM与葡萄糖-胰岛素动态平衡标志物之间的关系。研究设计和方法:对来自儿童围产期结局探索(EPOCH)研究的464名参与者,在儿童时期(~ 10年)进行了微阵列基因分型。通过研究访问和医疗记录提取的重复测量,对儿童和青少年时期的BMI轨迹进行了表征。葡萄糖-胰岛素稳态的标志物来自青春期(~ 16岁)的一次口服葡萄糖耐量试验。线性模型评估GLP-1R多态性对效果的影响。结果:在至少有一个rs10305420 (CT或TT)或rs1042044 (CA或AA)的次要等位基因,但没有主要等位基因纯合子的年轻人中,暴露于GDM与较高的平均BMI相关。对于rs6923761,暴露于GDM并且是主要等位基因纯合子(即基因型GG)的参与者的平均BMI显著高于队列中所有其他参与者。在青春期,没有多态性改变GDM和葡萄糖-胰岛素稳态标记物之间的关系。结论:GLP-1R多态性改变了青少年GDM和BMI增长之间的关系。需要进一步的研究来重复这些发现,并更好地了解GLP-1R多态性导致后代BMI生长异质性的机制。
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CiteScore
29.50
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