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Meta-analysis of the association between transforming growth factor-beta polymorphisms and complications of coronary heart disease.


ABSTRACT: OBJECTIVE: To investigate the association between common transforming growth factor beta (TGF-?) single nucleotide polymorphisms (SNP) and significant complications of coronary heart disease (CHD). METHOD: We performed a meta-analysis of published case-control studies assessing the association of TGF-? SNPs with a range of CHD complications. A random effects model was used to calculate odds ratios and confidence intervals. Analyses were conducted for additive, dominant and recessive modes of inheritance. RESULTS: Six studies involving 5535 cases and 2970 controls examining the association of common SNPs in TGF-?1 with CHD were identified. Applying a dominant model of inheritance, three TGF-?1 SNPs were significantly associated with CHD complications: The T alleles of rs1800469 (OR?=?1.125, 95% CI 1.016-1.247, p?=?0.031) and rs1800470 (OR?=?1.146, 95% CI 1.026-1.279, p?=?0.021); and the C allele of rs1800471 (OR?=?1.207, 95% CI 1.037-1.406, p?=?0.021). CONCLUSION: This meta-analysis suggests that common genetic polymorphisms in TGF-?1 are associated with complications of CHD.

SUBMITTER: Morris DR 

PROVIDER: S-EPMC3360665 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

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Meta-analysis of the association between transforming growth factor-beta polymorphisms and complications of coronary heart disease.

Morris Dylan R DR   Moxon Joseph V JV   Biros Erik E   Krishna Smriti M SM   Golledge Jonathan J  

PloS one 20120525 5


<h4>Objective</h4>To investigate the association between common transforming growth factor beta (TGF-β) single nucleotide polymorphisms (SNP) and significant complications of coronary heart disease (CHD).<h4>Method</h4>We performed a meta-analysis of published case-control studies assessing the association of TGF-β SNPs with a range of CHD complications. A random effects model was used to calculate odds ratios and confidence intervals. Analyses were conducted for additive, dominant and recessive  ...[more]

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