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体重指数相关基因变异与成人体成分之间的关联:芬兰德队列研究。

Associations between body mass index-related genetic variants and adult body composition: The Fenland cohort study.

作者信息

Clifton E A D, Day F R, De Lucia Rolfe E, Forouhi N G, Brage S, Griffin S J, Wareham N J, Ong K K

机构信息

MRC Epidemiology Unit, University of Cambridge School of Clinical Medicine, Institute of Metabolic Science, Cambridge, UK.

Department of Public Health and Primary Care, Institute of Public Health, University of Cambridge, Cambridge, UK.

出版信息

Int J Obes (Lond). 2017 Apr;41(4):613-619. doi: 10.1038/ijo.2017.11. Epub 2017 Jan 18.

Abstract

BACKGROUND/OBJECTIVE: Body mass index (BMI) is a surrogate measure of adiposity but does not distinguish fat from lean or bone mass. The genetic determinants of BMI are thought to predominantly influence adiposity but this has not been confirmed. Here we characterise the association between BMI-related genetic variants and body composition in adults.

SUBJECTS/METHODS: Among 9667 adults aged 29-64 years from the Fenland study, a genetic risk score for BMI (BMI-GRS) was calculated for each individual as the weighted sum of BMI-increasing alleles across 96 reported BMI-related variants. Associations between the BMI-GRS and body composition, estimated by dual-energy X-ray absorptiometry (DXA) scans, were examined using age-adjusted linear regression models, separately by sex.

RESULTS

The BMI-GRS was positively associated with all fat, lean and bone variables. Across body regions, associations of the greatest magnitude were observed for adiposity variables, for example, for each s.d. increase in BMI-GRS predicted BMI, we observed a 0.90 s.d. (95% confidence interval (CI): 0.71, 1.09) increase in total fat mass for men (P=3.75 × 10) and a 0.96 s.d. (95% CI: 0.77, 1.16) increase for women (P=6.12 × 10). Associations of intermediate magnitude were observed with lean variables, for example, total lean mass: men: 0.68 s.d. (95% CI: 0.49, 0.86; P=1.91 × 10); women: 0.85 s.d. (95% CI: 0.65, 1.04; P=2.66 × 10) and of a lower magnitude with bone variables, for example, total bone mass: men: 0.39 s.d. (95% CI: 0.20, 0.58; P=5.69 × 10); women: 0.45 s.d. (95% CI: 0.26, 0.65; P=3.96 × 10). Nominally significant associations with BMI were observed for 28 single-nucleotide polymorphisms. All 28 were positively associated with fat mass and 13 showed adipose-specific effects.

CONCLUSIONS

In adults, genetic susceptibility to elevated BMI influences adiposity more than lean or bone mass. This mirrors the association between BMI and body composition. The BMI-GRS can be used to model the effects of measured BMI and adiposity on health and other outcomes.

摘要

背景/目的:体重指数(BMI)是肥胖的替代指标,但无法区分脂肪与瘦体重或骨量。BMI的遗传决定因素被认为主要影响肥胖,但尚未得到证实。在此,我们对成人中与BMI相关的基因变异和身体成分之间的关联进行了特征描述。

受试者/方法:在来自芬兰研究的9667名年龄在29至64岁的成年人中,为每个人计算了BMI的遗传风险评分(BMI-GRS),作为96个已报道的与BMI相关变异中增加BMI的等位基因的加权总和。使用年龄调整的线性回归模型,按性别分别检查BMI-GRS与通过双能X线吸收法(DXA)扫描估计的身体成分之间的关联。

结果

BMI-GRS与所有脂肪、瘦体重和骨量变量呈正相关。在身体各部位中,肥胖变量的关联程度最大,例如,BMI-GRS每增加1个标准差预测的BMI,男性的总脂肪量增加0.90个标准差(95%置信区间(CI):0.71,1.09)(P = 3.75×10),女性增加0.96个标准差(95%CI:0.77,1.16)(P = 6.12×10)。与瘦体重变量的关联程度中等,例如,总瘦体重:男性:0.68个标准差(95%CI:0.49,0.86;P = 1.91×10);女性:0.85个标准差(95%CI:0.65,1.04;P = 2.66×10),与骨量变量的关联程度较低,例如,总骨量:男性:0.39个标准差(95%CI:0.20,0.58;P = 5.69×10);女性:0.45个标准差(95%CI:0.26,0.65;P = 3.96×10)。观察到28个单核苷酸多态性与BMI存在名义上显著的关联。所有28个均与脂肪量呈正相关,其中13个显示出脂肪特异性效应。

结论

在成年人中,对BMI升高的遗传易感性对肥胖的影响大于对瘦体重或骨量的影响。这反映了BMI与身体成分之间的关联。BMI-GRS可用于模拟测量的BMI和肥胖对健康及其他结局的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c548/5382973/fe7a53b6d214/emss-70667-f001.jpg

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