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Association of AdipoQ gene variation (rs1501299) and oxidative stress with cardiovascular disease in North West Indian population of Punjabi women

Authors :
Amrita Jyot
Mahajan Mridula
Bhanwer A.J.S.
Matharoo Kawaljit
Source :
Journal of Medical Biochemistry, Vol 40, Iss 1, Pp 49-59 (2021)
Publication Year :
2021
Publisher :
Society of Medical Biochemists of Serbia, Belgrade, 2021.

Abstract

Background: Till to date whether adiponectin AdipoQ gene variation (rs 1501299) is associated with cardiovascular disease, still remains controversial. Therefore, we aimed to relate the SNP (rs1501299) of adiponectin gene and oxidative stress in context to CVD in Punjabi women of North West India. Methods: In the present case-control study menopausal women with CVD as cases (n=265) and menopausal women without CVD as controls (n=258) were recruited. Genotyping of rs1501299 single nucleotide polymorphism of adiponectin gene was carried out by RFLP-PCR analysis. Biochemical parameters were analyzed according to the standard procedures. Results: Distribution of homozygous TT genotype of normolipidemic (p=0.001) and hyperlipidemic (p=0.001) women with CVD was significantly more frequent as compared to women without CVD. rs1501299 T allele carriers with CVD also showed significant (p=0.001) higher frequency distribution as compared to women without CVD. Under recessive model of inheritance TT mutant type homozygotes conferred 9 fold higher risk p=0.001; OR= 9.60 (2.92-31.58) towards CVD susceptibility for MDA>1.50; 11 fold higher risk p=0.007; OR= 11.11 (1.49-82.83) towards CVD for LDL carbonyl protein>15.04 and 9 fold higher risk p=0.001; OR= 9.75 (2.30-41.22) towards CVD susceptibility for SOD≤5.55. Under logistic regression analysis oxidative stress and TT genotype were significantly correlated with CVD. Conclusions: Our study revealed significant association of AdipoQ (rs1501299) gene polymorphism and oxidative stress with cardiovascular disease in Punjabi women of North West India. However, additional studies are required to support these findings.

Details

Language :
English
ISSN :
14528258 and 14528266
Volume :
40
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Journal of Medical Biochemistry
Publication Type :
Academic Journal
Accession number :
edsdoj.503d7ba9d3948ae9292397812bb6fa8
Document Type :
article
Full Text :
https://doi.org/10.5937/jomb0-24704