Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Clinical Epidemiology Group, Steno Diabetes Center Copenhagen, Copenhagen, Denmark.
Int J Obes (Lond). 2021 Sep;45(9):2006-2015. doi: 10.1038/s41366-021-00869-4. Epub 2021 May 28.
Genetic predisposition and maternal body mass index (BMI) are risk factors for childhood adiposity, defined by either BMI or overweight. We aimed to investigate whether childhood-specific genetic risk scores (GRSs) for adiposity-related traits are associated with childhood adiposity independent of maternal BMI, or whether the associations are modified by maternal BMI.
We constructed a weighted 26-SNP child BMI-GRS and a weighted 17-SNP child obesity-GRS in overall 1674 genotyped children within the Danish National Birth Cohort. We applied a case-cohort (N = 1261) and exposure-based cohort (N = 912) sampling design. Using logistic regression models we estimated associations of the GRSs and child overweight at age 7 years and examined if the GRSs influence child adiposity independent of maternal BMI (per standard deviation units).
In the case-cohort design analysis, maternal BMI and the child GRSs were associated with increased odds for childhood overweight [OR for maternal BMI: 2.01 (95% CI: 1.86; 2.17), OR for child BMI-GRS: 1.56 (95% CI: 1.47; 1.66), and OR for child obesity-GRS 1.46 (95% CI: 1.37; 1.54)]. Adjustment for maternal BMI did not change the results, and there were no significant interactions between the GRSs and maternal BMI. However, in the exposure-based cohort design analysis, significant interactions between the child GRSs and maternal BMI on child overweight were observed, suggesting 0.85-0.87-fold attenuation on ORs of child overweight at higher values of maternal BMI and child GRS.
GRSs for childhood adiposity are strongly associated with childhood adiposity even when adjusted for maternal BMI, suggesting that the child-specific GRSs and maternal BMI contribute to childhood overweight independent of each other. However, high maternal BMI may attenuate the effects of child GRSs in children.
遗传易感性和母体体重指数(BMI)是儿童肥胖的危险因素,可通过 BMI 或超重来定义。我们旨在研究与肥胖相关特征的儿童特异性遗传风险评分(GRS)是否与儿童肥胖相关,而与母体 BMI 无关,或者这些关联是否受母体 BMI 的影响。
我们在丹麦国家出生队列中对 1674 名经过基因分型的儿童构建了一个加权的 26-SNP 儿童 BMI-GRS 和一个加权的 17-SNP 儿童肥胖-GRS。我们应用病例-队列(N=1261)和基于暴露的队列(N=912)抽样设计。我们使用逻辑回归模型估计 GRS 与 7 岁儿童超重的相关性,并检验 GRS 是否独立于母体 BMI 影响儿童肥胖(每标准偏差单位)。
在病例-队列设计分析中,母体 BMI 和儿童 GRS 与儿童超重的几率增加相关[母体 BMI 的比值比(OR):2.01(95%CI:1.86;2.17),儿童 BMI-GRS 的 OR:1.56(95%CI:1.47;1.66),儿童肥胖-GRS 的 OR:1.46(95%CI:1.37;1.54)]。调整母体 BMI 并没有改变结果,并且 GRS 与母体 BMI 之间没有显著的相互作用。然而,在基于暴露的队列设计分析中,观察到儿童 GRS 与母体 BMI 之间对儿童超重的显著交互作用,这表明在较高的母体 BMI 和儿童 GRS 值下,儿童超重的 OR 降低了 0.85-0.87 倍。
即使调整了母体 BMI,儿童肥胖的 GRS 与儿童肥胖也有很强的相关性,这表明儿童特异性 GRS 和母体 BMI 独立地促进了儿童超重。然而,高母体 BMI 可能会减弱儿童 GRS 的影响。