PMID- 23040216 OWN - NLM STAT- MEDLINE DCOM- 20130603 LR - 20221207 IS - 1879-2472 (Electronic) IS - 0049-3848 (Linking) VI - 130 IP - 5 DP - 2012 Nov TI - Relationship between NADPH oxidase p22phox C242T, PARP-1 Val762Ala polymorphisms, angiographically verified coronary artery disease and myocardial infarction in South Indian patients with type 2 diabetes mellitus. PG - e259-65 LID - S0049-3848(12)00744-X [pii] LID - 10.1016/j.thromres.2012.09.012 [doi] AB - INTRODUCTION: There has been compelling evidence for the role of oxidative stress in the pathogenesis of cardiovascular complications in type 2 diabetes mellitus (T2DM). We analyzed the association of C242T and Val762Ala polymorphisms of NADPH oxidase p22phox and poly (ADP-ribose) polymerase-1 (PARP-1) genes respectively with coronary artery disease (CAD) and its severity, myocardial infarction (MI) and cardiovascular risk factors in T2DM patients. MATERIALS AND METHODS: We screened 283 T2DM patients, inclusive of 160 with angiographically defined CAD, 73 with and 89 without MI and 121 T2DM individuals with no evidence of CAD for the two gene polymorphisms. RESULTS: The 242T and 762Ala alleles were significantly more frequent in T2DM subjects without CAD than those with CAD, thereby associating them with a significant protective effect against development of CAD [p=0.002 (C242T); 0.02 (Val762Ala)]. The association was further characterized by a relatively lower frequency of 242T and 762Ala alleles in T2DM patients with multi (MVD)/triple vessel disease respectively [p=0.003 (C242T); 0.02 (Val762Ala)]. Conversely, the genotype and allele frequencies of these polymorphisms were not significantly different in T2DM+CAD patients with or without MI. Stratification of risk by putative risk factors for CAD revealed a significant interaction with these polymorphisms. Multiple logistic regression analysis revealed a significant and independent association of C242T and Val762Ala polymorphisms and other putative risk factors with CAD/MVD in T2DM individuals. CONCLUSIONS: Our observations indicate a significant relationship between p22phox C242T and PARP-1 Val762Ala polymorphisms, CAD and its severity, but not with occurrence of MI in T2DM individuals with significant coronary stenoses. CI - Copyright (c) 2012 Elsevier Ltd. All rights reserved. FAU - Narne, Parimala AU - Narne P AD - Department of Genetics, Osmania University, Hyderabad, India. parimala_narne@yahoo.co.in FAU - Ponnaluri, Kamakshi Chaithri AU - Ponnaluri KC FAU - Singh, Shailender AU - Singh S FAU - Siraj, Mohammed AU - Siraj M FAU - Ishaq, Mohammed AU - Ishaq M LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20121002 PL - United States TA - Thromb Res JT - Thrombosis research JID - 0326377 RN - EC 1.6.3.- (NADPH Oxidases) RN - EC 1.6.3.1 (CYBA protein, human) RN - EC 2.4.2.30 (PARP1 protein, human) RN - EC 2.4.2.30 (Poly (ADP-Ribose) Polymerase-1) RN - EC 2.4.2.30 (Poly(ADP-ribose) Polymerases) SB - IM MH - Angiography MH - Asian People MH - Coronary Artery Disease/diagnosis/*enzymology/genetics MH - Diabetes Mellitus, Type 2/*enzymology/genetics MH - Female MH - Gene Frequency MH - Gene Pool MH - Genetic Predisposition to Disease MH - Genotype MH - Humans MH - Male MH - Myocardial Infarction/*enzymology/genetics MH - NADPH Oxidases/*genetics MH - Oxidative Stress/physiology MH - Poly (ADP-Ribose) Polymerase-1 MH - Poly(ADP-ribose) Polymerases/*genetics MH - Polymorphism, Single Nucleotide MH - Risk Factors EDAT- 2012/10/09 06:00 MHDA- 2013/06/05 06:00 CRDT- 2012/10/09 06:00 PHST- 2012/05/16 00:00 [received] PHST- 2012/07/25 00:00 [revised] PHST- 2012/09/18 00:00 [accepted] PHST- 2012/10/09 06:00 [entrez] PHST- 2012/10/09 06:00 [pubmed] PHST- 2013/06/05 06:00 [medline] AID - S0049-3848(12)00744-X [pii] AID - 10.1016/j.thromres.2012.09.012 [doi] PST - ppublish SO - Thromb Res. 2012 Nov;130(5):e259-65. doi: 10.1016/j.thromres.2012.09.012. Epub 2012 Oct 2.