Association of sedentary and physical activity behaviours with body composition: a genome-wide association and Mendelian randomisation study

被引:4
作者
Ramadan, Ferris A. [1 ]
Bea, Jennifer W. [2 ,3 ]
Garcia, David O. [4 ]
Ellingson, Katherine D. [1 ]
Canales, Robert A. [5 ]
Raichlen, David A. [6 ]
Klimentidis, Yann C. [1 ]
机构
[1] Univ Arizona, Dept Epidemiol & Biostat, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Med, Tucson, AZ 85721 USA
[3] Univ Arizona, Dept Nutr Sci, Tucson, AZ 85721 USA
[4] Univ Arizona, Dept Hlth Promot Sci, Tucson, AZ 85721 USA
[5] George Washington Univ, Milken Inst Publ Hlth, Washington, DC 20037 USA
[6] Univ Southern Calif, Dept Biol Sci, Los Angeles, CA 90007 USA
关键词
Physical Activity; Body Composition; Visceral Adipose Tissue; Mendelian Randomization; WEIGHT-GAIN; OBESITY PREVENTION; ADIPOSE-TISSUE; VISCERAL FAT; EXERCISE; METAANALYSIS; ADULTS; LOCI; TIME; INTENSITY;
D O I
10.1136/bmjsem-2021-001291
中图分类号
G8 [体育];
学科分类号
04 ; 0403 ;
摘要
Objectives Studies suggest that body composition can be independently improved through physical activity (PA). We performed a Mendelian randomisation (MR) study to test the incremental benefits of sedentary behaviour and various PA exposures on body composition outcomes as assessed by anthropometric indices, lean body mass (kg), body fat (%) and visceral adipose tissue (VAT) (kg). Methods Genetic instruments were identified for both self-reported and accelerometer-measured sedentary behaviour and PA. Outcomes included anthropometric and dual-energy X-ray absorptiometry measures of adiposity, extracted from the UK Biobank and the largest available consortia. Multivariable MR (MVMR) included educational attainment as a covariate to address potential confounding. Sensitivity analyses were evaluated for weak instrument bias and pleiotropic effects. Results We did not identify consistent associations between genetically predicted self-reported and accelerometer-measured sedentary behaviour and body composition outcomes. All analyses for self-reported moderate PA were null for body composition outcomes. Genetically predicted PA at higher intensities was protective against VAT in MR and MVMR analyses of both accelerometer-measured vigorous PA (MVMR beta=-0.15, 95% CI: -0.24 to -0.07, p<0.001) and self-reported participation in strenuous sports or other exercises (MVMR beta=-0.27, 95% CI: -0.52 to -0.01, p=0.034) was robust across several sensitivity analyses. Conclusions We did not identify evidence of a causal relationship between genetically predicted PA and body composition, with the exception of a putatively protective effect of higher-intensity PA on VAT. Protective effects of PA against VAT may support prior evidence of biological pathways through which PA decreases risk of downstream cardiometabolic diseases.
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