| Autor: |
Huang, Kang, Ma, Tianyi, Li, Qiang, Zhong, Zanrui, Zhou, Yilei, Zhang, Wei, Qin, Ting, Tang, Shilin, Zhong, Jianghua, Lu, Shijuan |
| Předmět: |
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| Zdroj: |
BMC Medical Genomics; 3/4/2024, Vol. 17 Issue 1, p1-10, 10p |
| Abstrakt: |
Background: Coronary heart disease (CHD) has become a worldwide public health problem. Genetic factors are considered important risk factors for CHD. The aim of this study was to explore the correlation between CYP4A22 gene polymorphism and CHD susceptibility in the Chinese Han population. Methods: We used SNPStats online software to complete the association analysis among 962 volunteers. False-positive report probability analysis was used to confirm whether a positive result is noteworthy. Haploview software and SNPStats were used for haplotype analysis and linkage disequilibrium. Multi-factor dimensionality reduction was applied to evaluate the interaction between candidate SNPs. Results: In overall and some stratified analyses (male, age ≤ 60 years or CHD patients complicated with hypertension), CYP4A22-rs12564525 (overall, OR = 0.83, p-value is 0.042) and CYP4A22-rs2056900 (overall, OR = 1.22, p-value is 0.032) were associated with the risk of CHD. CYP4A22-4926581 was associated with increased CHD risk only in some stratified analyses. FPRP indicated that all positive results in our study are noteworthy findings. In addition, MDR showed that the single-locus model composed of rs2056900 is the best model for predicting susceptibility to CHD. Conclusion: There are significant associations between susceptibility to CHD and CYP4A22 rs12564525, and rs2056900. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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