[Study of the association between paraoxonase1 55 Met/Leu, paraoxonase2 148 Ala/Gly and manganese superoxide dismutase (MnSOD) 9 Ala/Val genetic polymorphisms and coronary heart disease].

Objective To study the associations between paraoxonase1 55 Met/Leu(PON1 55 Met/ Leu),paraoxonase2 148 Ala/Gly(PON2 148 Ala/Gly) and manganese superoxide dismutase 9 Ala/Val (MnSOD 9 Ala/Val) genetic polymorphisms and coronary heart disease (CHD), plasma activities of paraoxonase (PON),total superoxide dismutase(T-SOD),MnSOD,as well as plasma concentration of maleic dialdehyde(MDA). Methods Using PCR-RFLP method to identify genotype of PON1 55 Met/Leu, PON2 148 Ala/Gly and MnSOD 9 Ala/Val genetic polymorphisms, and using colorimetry to detect plasma activities of PON, T-SOD, MnSOD and plasma concentration of MDA in 262 CHD patients and 100 controls. Results Compared with controls,the plasma activities of PON[ (349.27±138.36 vs. 454. 75±166.00)nmol·min-1·ml-1,P0.001 ] ,T-SOD[(23.61±16. 51 us. 44.01±22.68)U/ml, P 0.001] and MnSOD[(21.56±13.11 vs. 28. 79±8. 65)U/ml, P0.001 ] reduced obviously, while plasma MDA concentration increased markedly [(2.47±0.73 vs. 2.15±0.55)nmol/ml, P0.01] in CHD patients. There were more LM genotype and Met allele of PON1 55 Met/Leu (24.8% vs. 1.4% ,P0.001 and 12.4% vs. 0.5% ,P = 0.001,respectively),GG and AG genotype and G allele of PON2 148 Ala/Gly (11.8% vs. 5.0%,P0.001,48.1% vs. 24.0% , P 0.001 and 36.0% vs. 17.0% , P 0.001, respectively) and AA genotype, A allele of MnSOD 9 Ala/Val genetic polymorphisms(64.2 % vs. 43. 0 % , P = 0. 001 and 80. 0 % vs . 67. 0 % , P = 0. 014 , respectively) in CHD patients than in controls. The activities of plasma PON and T-SOD were lower in individuals with PON, 55 LM genotype than those with LL genotype. The activity of plasma PON was also lower in individuals with PON2 148 GG/AG genotype than those with AA genotype. The activities of plasma PON and MnSOD depressed in individuals with MnSOD AA genotype compared with those with VV genotype. Logistic regression analysis demonstrated that PON, 55 LM genotype, PON2 148 GG/AG genotype and G allele were independent risk factors for CHD. Conclusion The antioxidative ability decreased, while lipid superoxide increased in CHD patients. Gene polymorphisms of PON1 55 Met/Leu , PON2 148 Ala/Gly and MnSOD 9 Ala/Val seemed to involve in the morbidity of CHD by influencing the plasma activities of PON and MnSOD.