Genetic Variant in the CYP19A1 Gene Associated with Coronary Artery Disease

Konstantina Bampali1, Charalampos Grassos2, Angeliki Mouzarou2

  • 1Department of Genetics and Biotechnology, Faculty of Biology, University of Athens, 15784 Athens, Greece.

Insights

The CYP19A1 gene's rs10046 polymorphism is linked to coronary artery disease (CAD). Individuals with the C allele have a higher likelihood of developing CAD, suggesting a genetic predisposition.

Area of Science:

  • Genetics
  • Cardiovascular Medicine
  • Molecular Biology

Background:

  • The CYP19A1 gene encodes aromatase, crucial for estrogen biosynthesis.
  • Previous research linked CYP19A1 rs10046 polymorphism to hypertension.
  • No studies have explored the association between CYP19A1 rs10046 and coronary artery disease (CAD).

Purpose of the Study:

  • To investigate the correlation between the CYP19A1 rs10046 (C/T) polymorphism and the occurrence of coronary artery disease (CAD).
  • To determine if specific genotypes or alleles of rs10046 are associated with an increased risk of developing CAD.

Main Methods:

  • Genotyping of the CYP19A1 rs10046 polymorphism in 189 subjects.
  • Categorization of subjects into a CAD patient group (123 individuals) and a healthy control group (66 individuals) based on coronary angiography.
  • Statistical analysis of genotype and allele frequencies between the patient and control groups.

Main Results:

  • Significant differences in genotype frequencies (CC, CT, TT) of rs10046 were observed between CAD patients and controls (P = 0.034).
  • The frequency of the C allele was significantly higher in the CAD group (0.58) compared to the control group (0.44) (P = 0.010).
  • Patients carrying the C allele demonstrated a 1.771-fold increased odds of having CAD (OR = 1.771).

Conclusions:

  • The rs10046 (C/T) polymorphism in the CYP19A1 gene is significantly associated with coronary artery disease (CAD).
  • The presence of the C allele confers an increased probability of developing CAD.
  • Further research is warranted, particularly in larger female cohorts, to confirm these findings.

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