Associations between genetic polymorphisms of paraoxonase genes and coronary artery disease in a Taiwanese population

Chi Ching Chen, Chien Chung Chen, Jun Da Tu, Yi Ling Wu, Sy Jye Leu

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Objective: We evaluated the relationship between polymorphisms of the paraoxonase (PON) gene and the risk of coronary artery disease (CAD) in Taiwanese patients. Methods: Our sample set included 369 volunteers, classified into two groups: 162 healthy volunteers and 207 CAD patients aged 60.0. ±. 9.7 and 64.3. ±. 12.3. years, respectively. Polymorphisms of the PON1 and PON2 genes were determined using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) techniques. Results: The results indicate that for the PON1 gene, the homozygous genotype RR was found significantly more often among the CAD group compared with the healthy group (OR. = 1.965, 95% CI. = 1.223-3.159, p. = 0.005). Furthermore, for the PON2 gene, the homozygous genotype CC was found significantly more often among the CAD group compared with the control group (OR. = 2.525, 95% CI. = 1.103-5.780, p. = 0.026). Conclusions: Individuals homozygous for the R allele of the PON1 gene and the C allele of the PON2 gene are more likely to have an increased risk of CAD.

Original languageEnglish
Pages (from-to)1664-1667
Number of pages4
JournalClinical Biochemistry
Issue number16-17
Publication statusPublished - Nov 2013



  • CAD
  • Gene polymorphisms
  • Paraoxonase
  • PON1
  • PON2

ASJC Scopus subject areas

  • Clinical Biochemistry

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