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儿童体重指数的新位点及其与成人心脏代谢特征的共享遗传度。

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.

机构信息

The Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.

Department of Pediatrics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.

出版信息

PLoS Genet. 2020 Oct 12;16(10):e1008718. doi: 10.1371/journal.pgen.1008718. eCollection 2020 Oct.

DOI:10.1371/journal.pgen.1008718
PMID:33045005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7581004/
Abstract

The genetic background of childhood body mass index (BMI), and the extent to which the well-known associations of childhood BMI with adult diseases are explained by shared genetic factors, are largely unknown. We performed a genome-wide association study meta-analysis of BMI in 61,111 children aged between 2 and 10 years. Twenty-five independent loci reached genome-wide significance in the combined discovery and replication analyses. Two of these, located near NEDD4L and SLC45A3, have not previously been reported in relation to either childhood or adult BMI. Positive genetic correlations of childhood BMI with birth weight and adult BMI, waist-to-hip ratio, diastolic blood pressure and type 2 diabetes were detected (Rg ranging from 0.11 to 0.76, P-values <0.002). A negative genetic correlation of childhood BMI with age at menarche was observed. Our results suggest that the biological processes underlying childhood BMI largely, but not completely, overlap with those underlying adult BMI. The well-known observational associations of BMI in childhood with cardio-metabolic diseases in adulthood may reflect partial genetic overlap, but in light of previous evidence, it is also likely that they are explained through phenotypic continuity of BMI from childhood into adulthood.

摘要

儿童体重指数(BMI)的遗传背景,以及儿童 BMI 与成人疾病的众所周知的相关性在多大程度上可以用共同的遗传因素来解释,这些在很大程度上是未知的。我们对 61111 名 2 至 10 岁儿童的 BMI 进行了全基因组关联研究荟萃分析。在联合发现和复制分析中,有 25 个独立的位点达到了全基因组显著水平。其中两个位于 NEDD4L 和 SLC45A3 附近,以前与儿童或成人 BMI 都没有关系。检测到儿童 BMI 与出生体重和成人 BMI、腰围与臀围比、舒张压和 2 型糖尿病之间存在正遗传相关性(Rg 范围为 0.11 至 0.76,P 值<0.002)。还观察到儿童 BMI 与初潮年龄之间存在负遗传相关性。我们的研究结果表明,儿童 BMI 所涉及的生物学过程在很大程度上与成人 BMI 所涉及的生物学过程重叠,但鉴于之前的证据,也有可能是通过 BMI 从儿童期到成年期的表型连续性来解释的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e012/7581004/6547f5717e41/pgen.1008718.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e012/7581004/5be87c0e3a3d/pgen.1008718.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e012/7581004/f900ca61d238/pgen.1008718.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e012/7581004/6c5da529cfd5/pgen.1008718.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e012/7581004/6547f5717e41/pgen.1008718.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e012/7581004/5be87c0e3a3d/pgen.1008718.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e012/7581004/f900ca61d238/pgen.1008718.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e012/7581004/6c5da529cfd5/pgen.1008718.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e012/7581004/6547f5717e41/pgen.1008718.g004.jpg

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