The Role of Polymorphisms Within Paraoxonases (192 Gln/Arg in PON1 and 311Ser/Cys in PON2) in the Modulation of Cardiovascular Risk: A Pilot Study

Author:

Gluba Anna1,Pietrucha Tadeusz2,Banach Maciej3,Piotrowski Grzegorz4,Rysz Jacek1

Affiliation:

1. Department of Nephrology, Hypertension and Family Medicine, Medical University of Lodz, Poland

2. Biotechnological Medicine, Medical University of Lodz, Poland

3. Department of Nephrology, Hypertension and Hypertension, Medical University of Lodz, Poland,

4. Department of Cardiology, M. Kopernik Provincial Specialist Hospital of Lodz, Poland

Abstract

Paraoxonases (PONs) may exert anti-atherogenic action by reducing lipid peroxidation. We evaluated the influence of 2 polymorphisms within PON1 (192 Gln/ Arg) and PON2 (311 Ser/Cys) genes in 407 young Poles: 273 patients who experienced a first myocardial infarction (MI) under the age of 45 (study group) and 134 healthy volunteers (control group) with a HEART Score ≤2 (low risk). Paraoxonase 1 polymorphism 192Gln/Arg influenced the risk of premature MI (P = .0054). A positive family history of coronary artery disease (CAD) was associated with the 192Arg allele (P = .0107). The association between PON1 genotype (192 Gln/Arg) and low-density lipoprotein cholesterol (LDL-C) (P = .036) levels was also observed. However, we did not find any relationship between polymorphism 311Ser/Cys and CAD risk (P = .418). PON1 polymorphism 192Gln/Arg influenced the risk of premature MI. The association between PON1 genotype (192 Gln/Arg) and serum LDL-C levels may be explained by PON participation in reverse cholesterol transport.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

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