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Apolipoprotein C3 gene variants and the risk of coronary heart disease: A meta-analysis
1Department of Epidemiology, Beijing An zhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing 100029, China.
Insights
This meta-analysis found that two apolipoprotein C3 gene single nucleotide polymorphisms (SNPs), SstI and T-455C, are associated with increased coronary heart disease (CHD) risk. Further studies are needed to confirm these findings on CHD risk factors.
Area of Science:
- Genetics and Cardiovascular Disease Research
- Molecular Epidemiology
- Biomarker Discovery
Background:
- Apolipoprotein C3 (APOC3) gene polymorphisms (SstI, C-482T, T-455C) have been implicated in coronary heart disease (CHD) risk.
- Previous studies show inconsistent results and potential ethnicity variations regarding these associations.
Purpose of the Study:
- To conduct a systematic meta-analysis evaluating the association between three APOC3 gene single nucleotide polymorphisms (SNPs) and the risk of CHD.
- To consolidate existing evidence and clarify the relationship between these genetic variations and cardiovascular risk.
Main Methods:
- Systematic literature search of HuGE Navigator and PubMed databases up to September 25, 2015.
- Data extraction and quality assessment by two independent reviewers.
- Random-effect model employed for meta-analysis to pool effect sizes.
Main Results:
- Included 29 studies with a total of 11,186 subjects for SstI, 3,727 for C-482T, and 6,753 for T-455C.
- Significant increase in CHD risk observed for SstI polymorphism (S2 vs. S1: OR=1.30, 95% CI 1.10-1.55).
- Significant increasing trend of CHD risk found for T-455C polymorphism (C vs. T: OR=1.28, 95% CI 1.16-1.41).
- No significant association found between C-482T polymorphism and CHD risk.
Conclusions:
- Pooled evidence suggests SstI and T-455C SNPs in the APOC3 gene are associated with increased CHD risk.
- The C-482T SNP did not show a significant association with CHD risk in this meta-analysis.
- Further large-scale, well-designed studies are recommended to validate these findings due to limited sample size and heterogeneity.
Background:
It has been reported that three common loci, SstI, C-482T, and T-455C, in the apolipoprotein C3 (APOC3) gene might be associated with an increased risk of coronary heart disease (CHD). Considering the inconsistent results and ethnicity variations, we performed a systematic meta-analysis to evaluate the association between three single nucleotide polymorphisms (SNPs) and the risk of CHD.
Methods:
We searched HuGE Navigator and PubMed databases to screen for the related literature published before 25 September, 2015. Two independent reviewers extracted the data and assessed the study quality. A random-effect model was used to pool the effect size.
Results:
A total of 29 studies met inclusion criteria. Nineteen studies, including 11,186 subjects relative to SstI, five studies comprising 3727 subjects relative to C-482T, and nine studies with 6753 subjects relative to T-455C were included in the final analysis. A significant increase in CHD risk was observed in the SstI polymorphism (S2 versus S1: odds ratio [OR] = 1.30, 95% confidence interval [CI] 1.10-1.55. There was also a significant increasing trend of CHD risk in the T-455C polymorphism (C versus T: OR = 1.28, 95% CI 1.16-1.41. However, no associations between C-482T and CHD risk were found in this meta-analysis.
Conclusions:
The pooled evidence suggests that two SNPs (SstI and T-455C) are associated with an increased risk of CHD. However, because of the limited sample size and heterogeneity, further large-scale and well-designed studies are needed to validate our findings.
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