Absence of association between CD86 +1057G/A polymorphism and coronary artery disease
Xiao-Na Ma1, Xia Wang, You-Yi Yan
1West China School of Preclinical and Forensic Medicine, West China Second University Hospital, Sichuan University, Chengdu, PR China.
Insights
This study found no link between the CD86 +1057G/A gene variant and coronary artery disease (CAD) risk in the Chinese population. Further research is needed to explore other genetic factors in CAD development.
Area of Science:
- Immunology
- Cardiovascular Disease Genetics
Background:
- CD86 is a crucial costimulatory molecule in T-cell immunity.
- CD86 also plays a role in the pathogenesis of cardiovascular diseases.
Purpose of the Study:
- To investigate the association between CD86 gene polymorphism and coronary artery disease (CAD) risk.
- Focus on the CD86 +1057G/A (rs1129055) single-nucleotide polymorphism in a Chinese population.
Main Methods:
- Genotyping of CD86 +1057G/A polymorphism using polymerase chain reaction-restriction fragment length polymorphism.
- DNA sequencing assay for confirmation.
- Case-control study involving 164 CAD patients and 299 healthy controls.
Main Results:
- No significant difference in genotype frequencies of CD86 +1057G/A polymorphism between CAD cases and controls.
- No significant difference in allele frequencies of CD86 +1057G/A polymorphism between CAD cases and controls.
Conclusions:
- The CD86 +1057G/A polymorphism is unlikely to be associated with CAD risk in the studied Chinese population.
- Genetic contributions to CAD require further investigation beyond this specific CD86 variant.
Abstract:
CD86, one of the key costimulatory molecules, is not only involved in the initiation of T-cell immunity but also plays important roles in the development of cardiovascular diseases. The purpose of this study was to investigate the association between the CD86 polymorphism and the risk of coronary artery disease (CAD) in a Chinese population. We analyzed single-nucleotide polymorphism of CD86 +1057G/A (rs1129055) in 164 patients with CAD and 299 healthy controls by performing polymerase chain reaction-restriction fragment length polymorphism and DNA sequencing assay. No significant association was observed in the genotype and allele frequencies of +1057G/A polymorphism between cases and controls, indicating that CD86 +1057G/A polymorphism may not be associated with CAD in the Chinese population.
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