Mapping the landscape of childhood obesity: genomic insights and socioeconomic status in Indian school-going children

IF 4.7 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Obesity Pub Date : 2025-02-25 DOI:10.1002/oby.24248
Janaki M. Nair, Ganesh Chauhan, Gauri Prasad, Khushdeep Bandesh, Anil K. Giri, Shraddha Chakraborty, Raman K. Marwaha, Sandeep Mathur, Devapriya Choudhury, Nikhil Tandon, Analabha Basu, Dwaipayan Bharadwaj
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引用次数: 0

Abstract

Objective

Childhood obesity (OB) is influenced by complex gene–environmental interaction. While genetics of adult OB have been extensively studied, polygenic childhood OB in non-European populations is still underexplored. Furthermore, in a developing nation such as India, how the environmental component strongly modulated by the socioeconomic status (SES) shapes the genetic susceptibility is crucial to understand.

Methods

A two-staged genome-wide association study (GWAS; N = 5673) and an independent exome-wide association study (ExWAS; N = 4963) were performed using a generalized linear model assuming additive effect to identify the common and rare genetic variants respectively associated with childhood OB. Rare-variant burden testing was also performed. We used the gene expression profiles and regulatory data from public databases to explain the novel associations. The implications of SES as a potential modifier of genetic susceptibility were evaluated.

Results

GWAS identified novel associations in TCF7L2, IMMP2L, IPMK, CDC5L, SNTG1, and MX1, whereas ExWAS uncovered CNTN4, COQ4, TNFRSF10D, FLG-AS1, and BMP3. Both GWAS and ExWAS validated known associations in FTO and MC4R. Furthermore, rare-variant testing highlighted the role of 101 genes. We also observed that SES can modulate the inherent susceptibility to OB.

Conclusions

Our study identified genetic variants associated with childhood OB and highlighted the gene–environmental interaction in childhood OB.

绘制儿童肥胖的景观:基因组的见解和印度学龄儿童的社会经济地位。
目的:儿童肥胖受复杂的基因-环境相互作用的影响。虽然成人OB的遗传学已被广泛研究,但非欧洲人群的多基因儿童OB仍未得到充分研究。此外,在像印度这样的发展中国家,社会经济地位(SES)对环境因素的强烈调节如何塑造遗传易感性是至关重要的。方法:两阶段全基因组关联研究(GWAS;N = 5673)和独立的外显子组关联研究(ExWAS;N = 4963)采用假定加性效应的广义线性模型分别识别与儿童OB相关的常见和罕见遗传变异。还进行了罕见变异负担测试。我们使用来自公共数据库的基因表达谱和调控数据来解释新的关联。评价了SES作为遗传易感性潜在修饰因子的意义。结果:GWAS发现了TCF7L2、IMMP2L、IPMK、CDC5L、SNTG1和MX1的新关联,而ExWAS发现了CNTN4、COQ4、TNFRSF10D、FLG-AS1和BMP3。GWAS和ExWAS都证实了FTO和MC4R的已知关联。此外,罕见变异测试强调了101个基因的作用。我们还观察到SES可以调节OB的固有易感性。结论:我们的研究发现了与儿童OB相关的遗传变异,并强调了儿童OB的基因-环境相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Obesity
Obesity 医学-内分泌学与代谢
CiteScore
11.70
自引率
1.40%
发文量
261
审稿时长
2-4 weeks
期刊介绍: Obesity is the official journal of The Obesity Society and is the premier source of information for increasing knowledge, fostering translational research from basic to population science, and promoting better treatment for people with obesity. Obesity publishes important peer-reviewed research and cutting-edge reviews, commentaries, and public health and medical developments.
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