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. 2017 Jun 13;135(24):2373-2388.
doi: 10.1161/CIRCULATIONAHA.116.026560. Epub 2017 May 12.

Causal Associations of Adiposity and Body Fat Distribution With Coronary Heart Disease, Stroke Subtypes, and Type 2 Diabetes Mellitus: A Mendelian Randomization Analysis

Affiliations

Causal Associations of Adiposity and Body Fat Distribution With Coronary Heart Disease, Stroke Subtypes, and Type 2 Diabetes Mellitus: A Mendelian Randomization Analysis

Caroline E Dale et al. Circulation. .

Abstract

Background: The implications of different adiposity measures on cardiovascular disease etiology remain unclear. In this article, we quantify and contrast causal associations of central adiposity (waist-to-hip ratio adjusted for body mass index [WHRadjBMI]) and general adiposity (body mass index [BMI]) with cardiometabolic disease.

Methods: Ninety-seven independent single-nucleotide polymorphisms for BMI and 49 single-nucleotide polymorphisms for WHRadjBMI were used to conduct Mendelian randomization analyses in 14 prospective studies supplemented with coronary heart disease (CHD) data from CARDIoGRAMplusC4D (Coronary Artery Disease Genome-wide Replication and Meta-analysis [CARDIoGRAM] plus The Coronary Artery Disease [C4D] Genetics; combined total 66 842 cases), stroke from METASTROKE (12 389 ischemic stroke cases), type 2 diabetes mellitus from DIAGRAM (Diabetes Genetics Replication and Meta-analysis; 34 840 cases), and lipids from GLGC (Global Lipids Genetic Consortium; 213 500 participants) consortia. Primary outcomes were CHD, type 2 diabetes mellitus, and major stroke subtypes; secondary analyses included 18 cardiometabolic traits.

Results: Each one standard deviation (SD) higher WHRadjBMI (1 SD≈0.08 U) associated with a 48% excess risk of CHD (odds ratio [OR] for CHD, 1.48; 95% confidence interval [CI], 1.28-1.71), similar to findings for BMI (1 SD≈4.6 kg/m2; OR for CHD, 1.36; 95% CI, 1.22-1.52). Only WHRadjBMI increased risk of ischemic stroke (OR, 1.32; 95% CI, 1.03-1.70). For type 2 diabetes mellitus, both measures had large effects: OR, 1.82 (95% CI, 1.38-2.42) and OR, 1.98 (95% CI, 1.41-2.78) per 1 SD higher WHRadjBMI and BMI, respectively. Both WHRadjBMI and BMI were associated with higher left ventricular hypertrophy, glycemic traits, interleukin 6, and circulating lipids. WHRadjBMI was also associated with higher carotid intima-media thickness (39%; 95% CI, 9%-77% per 1 SD).

Conclusions: Both general and central adiposity have causal effects on CHD and type 2 diabetes mellitus. Central adiposity may have a stronger effect on stroke risk. Future estimates of the burden of adiposity on health should include measures of central and general adiposity.

Keywords: Mendelian randomization analysis; adiposity; body fat distribution; body mass index; coronary artery disease; stroke; waist-hip ratio.

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Figures

Figure 1a
Figure 1a. Association of BMI with continuous biomarkers derived from Mendelian randomization analysis.
Values represent standardized mean differences of each trait per SD increase in BMI derived from conventional (IVW) Mendelian randomization analysis. Non-normally distributed variables were natural ln transformed; therefore mean differences displayed on the log scale may be anti-logged and interpreted as percentage differences in SD of trait per SD in BMI. Log triglycerides from individual participant data studies only; GLGC triglycerides in Supplemental Table 10.
Figure 1b
Figure 1b. Association of WHRadjBMI with continuous biomarkers derived from Mendelian randomization analysis.
Values represent standardized mean differences of each trait per SD increase in WHRadjBMI derived from conventional (IVW) Mendelian randomization analysis. Non-normally distributed variables were natural log transformed; therefore mean differences displayed on the log scale may be anti-logged and interpreted as percentage difference in SD of trait per SD in WHRadjBMI. Log triglycerides from individual participant data studies only; GLGC triglycerides in Supplemental Table 11.
Figure 2a
Figure 2a. Associations of adiposity with risk of CHD from observational and Mendelian randomization analyses.
Association between coronary heart disease and adiposity (BMI and WHRadjBMI) comparing causal odds ratios (OR) per SD of adiposity trait derived from instrumental variable analysis and observational analysis from the Emerging Risk Factors Consortium hazard ratio (HR per SD of BMI or waist:hip adjusted for age, sex and smoking status). Causal estimates are derived from Mendelian randomization and include conventional (ratio) approach and weighted median (see Methods for further details). P(genetic pleiotropy) relates to the P-value derived from the intercept of MR-Egger; a small P-value denotes presence of directional pleiotropy.
Figure 2b
Figure 2b. Associations of adiposity with risk of ischaemic stroke from observational and Mendelian randomization analyses.
Association between ischaemic stroke and adiposity (BMI and WHRadjBMI) comparing causal odds ratios (OR) per SD of adiposity trait derived from instrumental variable analysis and observational analysis from the Emerging Risk Factors Consortium (HR of ischaemic stroke per SD of BMI or waist:hip adjusted for age, sex and smoking status). Causal estimates are derived from Mendelian randomization and include conventional (ratio) approach and weighted median (see Methods for further details). P(genetic pleiotropy) relates to the P-value derived from the intercept of MR-Egger; a small P-value denotes presence of directional pleiotropy.
Figure 2c
Figure 2c. Associations of adiposity with risk of T2D from observational and Mendelian randomization analyses.
Association between T2D and adiposity (BMI and WHRadjBMI) comparing causal odds ratios (OR) per SD of adiposity trait derived from instrumental variable analysis and observational analysis from Vazquez et al., 2007. Causal estimates are derived from Mendelian randomization and include conventional (ratio) approach and weighted median (see Methods for further details). P(genetic pleiotropy) relates to the P-value derived from the intercept of MR-Egger; a small P-value denotes presence of directional pleiotropy.

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