Genetic Variations of Angiotensinogen, Angiotensin Converting Enzyme, and Angiotensin Type 1 Receptor with the Risk of Pulmonary Tuberculosis
Language English Country Czech Republic Media print
Document type Journal Article
Grant support
ZMG #8299
Zahedan University of Medical Sciences
PubMed
38380450
DOI
10.14712/23362936.2024.1
PII: pmr_2024125010005
Knihovny.cz E-resources
- Keywords
- Angiotensin, Angiotensin converting enzyme, Angiotensin type 1 receptor, Polymorphism, Tuberculosis,
- MeSH
- Peptidyl-Dipeptidase A * genetics MeSH
- Angiotensinogen genetics MeSH
- Genetic Predisposition to Disease MeSH
- Genotype MeSH
- Humans MeSH
- Tuberculosis, Pulmonary * genetics MeSH
- Polymorphism, Genetic MeSH
- Receptor, Angiotensin, Type 1 genetics MeSH
- Case-Control Studies MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Iran epidemiology MeSH
- Names of Substances
- ACE protein, human MeSH Browser
- AGT protein, human MeSH Browser
- AGTR1 protein, human MeSH Browser
- Peptidyl-Dipeptidase A * MeSH
- Angiotensinogen MeSH
- Receptor, Angiotensin, Type 1 MeSH
There is little data regarding the impact of renin-angiotensin system (RAS) gene polymorphisms on tuberculosis. The current study designed to survey the possible association between RAS polymorphisms and the risk of pulmonary tuberculosis (PTB) in a sample of the southeast Iranian population. This case-control study was done on 170 PTB patients and 170 healthy subjects. The AGT rs699 C>T, ACE rs4341 C>G and AT1R rs5186 C>A variants were genotyped using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) and ACE rs4646994 (287bp I/D) variant by PCR method. Regarding AT1R rs5186 A>C polymorphism, the findings revealed that AC genotype and C allele significantly decreased the risk of PTB (OR=0.39, 95% CI=0.22-0.67, p=0.001, and OR=0.53, 95% CI=0.25-0.72, p=0.002, C vs. A, respectively). The TC genotype and C allele of AGT rs699 T>C significantly associated with decreased the risk of PTB (OR=0.45, 95% CI=0.28-0.74, p=0.002, TC vs. TT and OR=0.51, 95% CI=0.32-0.80, p=0.005, C vs. T, respectively). The ID genotype of ACE 287bp I/D significantly increased the risk of PTB (OR=1.88, 95% CI=1.12-3.17, p=0.017). Our finding did not support an association between ACE rs4341 C>G variant and the risk of PTB. In summary, the findings revealed an association between AT1R rs5186 A>C, AGT rs699 T>C and ACE 287bp I/D polymorphisms and the risk of PTB in a sample of the southeast Iranian population. Further investigation with higher sample sizes and diverse ethnicities are required to confirm our findings.
Children and Adolescent Health Research Center Zahedan University of Medical Sciences Zahedan Iran
Department of Genetic School of Medicine Zahedan University of Medical Sciences Zahedan Iran
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