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No association between vitamin D receptor polymorphisms and coronary artery disease in a Chinese population
Xin-Min Pan1, Dong-Ri Li, Lan Yang
1Department of Forensic Pathology, West China School of Preclinical and Forensic Medicine, Sichuan University , Chengdu, Peoples' Republic of China .
Insights
Genetic factors influence coronary artery disease (CAD) risk. This study found no significant association between vitamin D receptor (VDR) gene polymorphisms (FokI and BsmI) and CAD in the Chinese population.
Area of Science:
- Genetics
- Cardiology
- Molecular Biology
Background:
- Clinical observations suggest a strong genetic predisposition to coronary artery disease (CAD).
- The vitamin D receptor (VDR) gene is a potential candidate for influencing CAD susceptibility.
- Specific polymorphisms in the VDR gene, FokI and BsmI, have been investigated for their role in various diseases.
Purpose of the Study:
- To investigate the association between FokI (rs2228570) and BsmI (rs1544410) polymorphisms of the VDR gene and the risk of coronary artery disease (CAD).
- To analyze genotype and allele frequencies of these VDR polymorphisms in a Chinese population with and without CAD.
Main Methods:
- Case-control study design.
- Genotyping of 152 CAD patients and 212 healthy controls using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) for VDR FokI and BsmI polymorphisms.
- Statistical analysis of genotype and allele frequencies.
Main Results:
- No statistically significant differences were found in the genotype frequencies of FokI and BsmI polymorphisms between CAD patients and healthy controls.
- Allele frequencies for both FokI and BsmI VDR gene polymorphisms did not show significant variation between the case and control groups.
- Odds ratios for FokI (1.11) and BsmI (0.74) indicated no substantial association with CAD risk in this Chinese cohort.
Conclusions:
- The FokI and BsmI polymorphisms in the vitamin D receptor (VDR) gene are not significantly associated with coronary artery disease (CAD) susceptibility in the studied Chinese population.
- These specific VDR gene variants do not appear to be major genetic risk factors for CAD in this demographic.
- Further research with larger cohorts and different populations may be warranted to fully elucidate the role of VDR gene variations in CAD.
Abstract:
The clinical features suggest that genetic factors may have a strong influence on susceptibility to coronary artery disease (CAD). The aim of this study was to investigate the association between FokI (rs2228570) and BsmI (rs1544410) of the vitamin D receptor (VDR) gene polymorphisms and patients with CAD in a Chinese population. One hundred and fifty-two CAD patients and 212 healthy controls were genotyped for the FokI and BsmI polymorphisms in VDR gene using polymerase chain reaction-restriction fragment length polymorphism. No significant differences were observed in the genotype and allele frequencies of the FokI and BsmI polymorphisms between the cases and controls (For FokI: odds ratio = 1.11, 95% confidence interval 0.83-1.50; for BsmI: odds ratio = 0.74, 95% confidence interval 0.44-1.23). There was no significant difference in the genotype distribution or the allele frequencies of VDR FokI and BsmI between two groups in a Chinese population.
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