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Submitted: 13 Feb 2023
Revision: 02 Jul 2023
Accepted: 29 Jul 2023
ePublished: 23 Sep 2023
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J Cardiovasc Thorac Res. 2023;15(3): 168-173.
doi: 10.34172/jcvtr.2023.31742
PMID: 38028723
PMCID: PMC10590467
  Abstract View: 475
  PDF Download: 486
  Full Text View: 322

Original Article

Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population

Golnaz Houshmand 1 ORCID logo, Mohammad Javad Alemzadeh-Ansari 2 ORCID logo, Saeideh Mazloumzadeh 1 ORCID logo, Niloofar Naderi 3, Maryam Pourirahim 3, Katayoun Heshmatzad 1, Majid Maleki 3, Samira Kalayinia 3* ORCID logo

1 Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
2 Cardiovascular Intervention Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
3 Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
*Corresponding Author: Samira Kalayinia, Email: samira.kalayi@yahoo.com

Abstract

Introduction: Coronary artery disease (CAD) is the leading health complication worldwide because of its high prevalence and mortality. The association between CAD susceptibility and the rs599839 (C/T) polymorphism in the human proline and serine-rich coiled-coil (PSRC1) was reported in a genome-wide association study. To validate this association, we performed this case-control study to genotype the 1p13.3 (rs599839) locus in a sample of the Iranian population with CAD (stenosis≥70% in≥1 coronary artery).

Methods: We performed an association analysis with PCR and Sanger sequencing of rs599839 (C/T) polymorphism and CAD risk in 280 CAD patients and 287 healthy controls defined as a coronary calcium score of zero and no noncalcified plaques in coronary computed tomography angiography. SPSS, version 16.0, was applied for statistical analysis.

Results: The rs599839 (C/T) locus showed a significant association with CAD (P value<0.001). TT and CT genotypes were associated with CAD (P value<0.001). Furthermore, the dominant status (TT+CT vs. CC) was associated with an increased risk of CAD (OR, 9.14; 95% CI, 3.77 to 22.15; and P value<0.001).

Conclusion: The study findings indicate strong evidence for rs599839 (C/T) association with CAD risk.

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