Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2164-14-867
Title: Association of homocysteine with type 2 diabetes: A meta-analysis implementing Mendelian randomization approach
Authors: Huang, T 
Ren, J
Huang, J
Li, D
Keywords: 5,10 methylenetetrahydrofolate reductase (FADH2)
homocysteine
allele
amino acid blood level
article
causal attribution
controlled study
genotype
human
major clinical study
Mendelian randomization analysis
non insulin dependent diabetes mellitus
risk assessment
Alleles
Diabetes Mellitus, Type 2
Genetic Predisposition to Disease
Genotype
Homocysteine
Humans
Mendelian Randomization Analysis
Methylenetetrahydrofolate Reductase (NADPH2)
Risk Factors
Issue Date: 2013
Citation: Huang, T, Ren, J, Huang, J, Li, D (2013). Association of homocysteine with type 2 diabetes: A meta-analysis implementing Mendelian randomization approach. BMC Genomics 14 (1) : 867. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2164-14-867
Rights: Attribution 4.0 International
Abstract: Background: We tested the hypothesis that elevated homocysteine (Hcy) level is causally associated with increased risk of type 2 diabetes mellitus (T2DM). Results: The meta-analysis and Mendelian randomization analysis were performed among 4011 cases and 4303 controls. The absolute pooled mean Hcy concentration in subjects with MTHFR 677TT was 5.55 μmol/L (95% CI, 1.33 to 9.77) greater than that in subjects with MTHFR 677CC in T2DM. Overall, the T allele of the MTHFR 677 C > T conferred a greater risk for T2DM [Random effect (RE) OR = 1.31(1.17-1.64), I2 = 41.0%, p = 0.055]. The random effect (RE) pooled OR associated with T2DM for MTHFR 677TT relative to the 677CC was [RE OR = 1.38(1.18-1.62)]. The fixed-effect pooled OR of the association for the MTHFR 677 TT vs CT was 1.29 (95% CI, 1.09-1.51). MTHFR 677 TT showed a significantly higher risk for T2DM compared with MTHFR 677 CC + CT [Fixed effect (FE) OR = 1.32(1.14-1.54), I2 = 0.0%, p = 0.686]. The absolute pooled mean Hcy concentration in individuals with T2DM was 0.94 μmol/L (95% CI, 0.40-1.48) greater than that in control subjects. The estimated causal OR associated with T2DM was 1.29 for 5 μmol/L increment in Hcy. Conclusions: Our findings provided strong evidence on the causal association of Hcy level with the development of T2DM. © 2013 Huang et al.; licensee BioMed Central Ltd.
Source Title: BMC Genomics
URI: https://scholarbank.nus.edu.sg/handle/10635/181537
ISSN: 14712164
DOI: 10.1186/1471-2164-14-867
Rights: Attribution 4.0 International
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