Key result
Carrying the T allele of the TGF-beta 509C/T polymorphism (rs1800469) is associated with a 13% increased risk of myocardial infarction compared to C allele carriers (OR 1.13).
Why the study?
Studies evaluating the association between the TGF-beta-509C/T (rs1800469) promoter polymorphism and myocardial infarction risk have reported inconsistent results.
Does the TGF-β 509C/T (rs1800469) polymorphism increase the risk of myocardial infarction?
Meta-Analysis (n=13,873)
Does the TGF-β 509C/T (rs1800469) polymorphism increase the risk of myocardial infarction?
Odds Ratio: 1.13 (95% CI 1–1.27)
The TGF-β 509C/T (rs1800469) polymorphism, specifically the T allele, is significantly associated with an increased risk of myocardial infarction.
Does not support routine genetic testing for MI risk; leaves open whether this variant improves prediction beyond clinical factors.
Studies investigating the association between transforming growth factor (TGF-β-509C/T, rs1800469) promoter polymorphism and myocardial infarction (MI) risk reported inconsistent results. The aim of our study was to assess the association between the 509C/T polymorphism of the TGF-β gene (rs1800469) and MI risk.A total of 5460 cases and 8413 controls in 7 case-control studies were incorporated in our current meta-analysis. The original studies were selected through searching the databases of the PubMed and EMBASE. The odds ratio (OR) and 95% confidence interval (95% CI) of TGF-β 509C/T (rs1800469) for MI risk were applied to estimate the strength of the association.Our results showed that T allele carriers had a 13% increased risk of MI, when compared with the C allele carriers (OR = 1.13, 95% CI: 1.00-1.27). In the subset analysis by the type of MI, significantly elevated risk of MI was associated with the homozygote TT and heterozygote C/T in no-AMI subjects, when compared with the CC homozygote carriers (OR = 1.12, 95% CI:1.02-1.23).Our meta-analysis shows that the polymorphism with homozygote TT and heterozygote C/T of TGF-β 509C/T (rs1800469) is significantly associated with the increased risk of MI.
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Du et al. (2019) conducted a meta-analysis in Myocardial infarction (n=13,873). TGF-beta 509C/T polymorphism (rs1800469) T allele vs. C allele carriers was evaluated on Risk of myocardial infarction (OR 1.13, 95% CI 1.00-1.27). Carrying the T allele of the TGF-beta 509C/T polymorphism (rs1800469) is associated with a 13% increased risk of myocardial infarction compared to C allele carriers (OR 1.13).
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