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Background

Coronary artery disease (CAD) is a complex disease resulting from the cumulative and interactive effects of large number of genes along with environmental exposure. Therefore, the present study was envisaged as an effort to study the association of candidate genes ESR1 (rs2234693 and rs9340799), CETP (rs708272), MTHFR (rs1801133 and rs2274976) and MS (rs185087) polymorphisms with the risk of CAD, targeting the populations of Jammu (JandK).

Method

A total of 400 confirmed CAD patients and 400 healthy controls were enrolled for the present study. Genotyping was done by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).

Results

ESR1 gene (rs9340799) polymorphism was found to be associated with CAD in all the genetic models. The haplotype analysis of ESR1 (rs2234693 and rs9340799) gene revealed that C-G haplotype was conferring approximately 5-fold risk and T-A haplotype was adding 1.4-fold risk towards the disease. 'T' allele of MTHFR rs1801133 SNP was observed to be responsible for development of CAD in our study population (p < 0.0001). In case of MTHFR (rs1801133 and rs2274976) gene, the haplotype T-G was observed to confer 4.7-fold risk towards CAD whereas haplotype C-G provided nearly a 1.7 fold protection towards development of CAD. For MS gene, rs185087 was also found to be associated with CAD in a co-dominant (p = 0.003 and p = 0.03), dominant (p = 0.001) and allelic models (p = 0.001). The gene-gene interaction revealed strong epistasis between single nucleotide polymorphisms (SNPs), ESR1 rs9340799 and MTHFR rs2274976. Furthermore, the dendrogram for gene-environment dataset indicated moderately synergistic interaction between CETP rs708272 and physical inactivity.

Conclusion

In the study under reference, a significant association of ESR1-XbaI (rs9340799), MTHFR C677T (rs1801133) and MS A2756G (rs185087) gene polymorphisms with the susceptibility of CAD in the population of Jammu region (JandK) has been observed."xsd:string
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http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/author"Kumar P."xsd:string
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/author"Sharma M."xsd:string
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/author"Panjaliya R.K."xsd:string
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/author"Dogra V."xsd:string
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/author"Bakaya A."xsd:string
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/author"Raina J.K."xsd:string
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/name"BMC Cardiovasc Disord"xsd:string
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/pages"340"xsd:string
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/title"Association of ESR1 (rs2234693 and rs9340799), CETP (rs708272), MTHFR (rs1801133 and rs2274976) and MS (rs185087) polymorphisms with Coronary Artery Disease (CAD)."xsd:string
http://purl.uniprot.org/citations/32682401http://purl.uniprot.org/core/volume"20"xsd:string
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