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Published on: December 7, 2013
A meta-analysis on correlations of OX40L variants with atherosclerotic disorders
Xiaoxu Wang1, Yaxin Luan1, Chengsen Zhang2
1Department of Cardiology, The Second Municipal Hospital of Weihai City, Weihai, Shandong, China.
Insights
Genetic variants in OX40 ligand (OX40L) show associations with atherosclerotic cardio-cerebral vascular diseases (ASCVD) in specific populations. Certain OX40L variants may serve as biomarkers for coronary artery disease (CAD) and acute coronary syndrome (ACS).
Area of Science:
- Genetics
- Cardiovascular Medicine
- Immunology
Background:
- Atherosclerotic cardio-cerebral vascular diseases (ASCVD) represent a significant global health burden.
- The role of genetic variations, specifically in OX40 ligand (OX40L), in the development of ASCVD requires further investigation.
Purpose of the Study:
- To conduct a meta-analysis investigating the correlations between OX40 ligand (OX40L) genetic variants and atherosclerotic cardio-cerebral vascular diseases (ASCVD).
- To identify potential genetic biomarkers for ASCVD subtypes.
Main Methods:
- Systematic literature search performed across PubMed, Medline, and Embase databases.
- Meta-analysis and statistical analyses conducted using Review Manager.
- Inclusion of eighteen studies for comprehensive analysis.
Main Results:
- Overall analysis showed no significant correlation between OX40L variants and ASCVD.
- Subgroup analysis by ethnicity revealed a significant association between the rs1234314 variant and ASCVD in East Asians.
- Specific variants (rs17568, rs1234314, rs3850641) showed significant associations with acute coronary syndrome (ACS) and coronary artery disease (CAD) subtypes.
Conclusions:
- The rs17568, rs1234314, and rs3850641 variants of OX40L may function as genetic biomarkers for specific types of coronary artery disease (CAD).
- Further research is warranted to elucidate the precise mechanisms underlying these genetic associations.
Background:
This meta-analysis was conducted to analyze the correlations of OX40 ligand (OX40L) variants with atherosclerotic cardio-cerebral vascular diseases (ASCVD).
Methods:
Systematic literature research was conducted in PubMed, Medline, and Embase. All statistical analyses were conducted with Review Manager.
Results:
Totally eighteen studies were enrolled for analyses. Although no any significant correlations between OX40L variants and ASCVD were detected in overall analyses. Further subgroup analyses by ethnicity revealed that rs1234314 variant was significantly associated with ASCVD in East Asians (dominant model: P = 0.03, odds ratios [OR] = 1.15, 95% confidence interval [CI], 1.01-1.31; allele model: P = 0.04, OR = 1.10, 95%CI, 1.00-1.20). When we stratified eligible studies by type of disease, positive results were observed for rs17568 variant in subjects with acute coronary syndrome (ACS) (allele model: P = 0.04, OR = 0.81, 95%CI, 0.65-0.99), for rs1234314 variant in subjects with coronary artery disease (CAD) (dominant model: P = 0.04, OR = 1.16, 95%CI, 1.00-1.35), for rs3850641 variant in subjects with CAD (recessive model: P = 0.02, OR = 1.42, 95%CI, 1.05-1.90) and myocardial infarction (MI) (recessive model: P = 0.03, OR = 1.49, 95%CI, 1.05-2.11).
Conclusions:
Our findings suggested that rs17568, rs1234314, and rs3850641 variants might serve as genetic biomarkers of certain types of CAD.
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