Plausible relationship between homocysteine and obesity risk via gene: a meta-analysis of 38,317 individuals implementing Mendelian randomization.

Diabetes Metab Syndr Obes

State Key Laboratory of Genetic Engineering, Institute of Biostatistics, School of Life Sciences, Fudan University, Shanghai, People's Republic of China.

Published: July 2019

Objective: Numerous studies have explored the role of methylenetetrahydrofolate reductase gene () C677T polymorphism and homocysteine (Hcy) concentration in obesity, but the results are inconsistent. Hence, we performed a meta-analysis implementing Mendelian randomization approach to test the assumption that the increased Hcy concentration is plausibly related to the elevated risk of obesity.

Methods: Eligible studies were selected based on several inclusion and exclusion criteria. Correlations between C677T and obesity risk, C677T and Hcy concentration in obesity, Hcy concentration, and obesity were estimated by ORs, effect size and standard mean difference with their corresponding 95% CIs, respectively. Furthermore, Mendelian randomization analysis was performed to estimate the relationship between Hcy level and obesity.

Results: Consequently, this meta-analysis implemented with Mendelian randomization approach was conducted among 8,622 cases and 29,695 controls. The results indicated that C677T is associated with an increased risk of obesity (for T vs C: OR=1.06, 95% CI=1.02-1.10; for TT vs CC: OR=1.13, 95% CI=1.03-1.24). Moreover, in obese subjects, the pooled Hcy concentration in individuals of TT genotype was 2.91 mmol/L (95% CI: 0.27-5.55) higher than that in individuals of CC genotype. Furthermore, the pooled Hcy concentration in subjects with obesity was 0.74 mmol/L (95% CI: 0.36-1.12) higher than that in controls. The evaluated plausible OR associated with obesity was 1.23 for 5 μmol/L Hcy level increase.

Conclusions: Through this meta-analysis, we emphasize a strong relationship between Hcy level and obesity by virtue of C677T polymorphism.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662519PMC
http://dx.doi.org/10.2147/DMSO.S205379DOI Listing

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