PMID- 27608594 OWN - NLM STAT- MEDLINE DCOM- 20180430 LR - 20180508 IS - 1878-3279 (Electronic) IS - 0171-2985 (Linking) VI - 222 IP - 10 DP - 2017 Oct TI - PLA2G2A polymorphisms are associated with metabolic syndrome and type 2 diabetes mellitus. Results from the genetics of atherosclerotic disease Mexican study. PG - 967-972 LID - S0171-2985(16)30361-8 [pii] LID - 10.1016/j.imbio.2016.08.014 [doi] AB - The secretory phospholipase A(2) II A (sPLA(2)-IIA) encoded by PLA2G2A gene hydrolyzes phospholipids liberating free fatty acids (FFAs) and lysophospholipids. If lipolysis exceeds lipogenesis, the free fatty acids undergo a continuous release into circulation. A sustained excessive increase in this release contributes to metabolic disease. The aim of the present study was to evaluate the role of PLA2G2A gene polymorphisms as susceptibility markers for metabolic syndrome (MetS) and type 2 diabetes mellitus (T2DM) in Mexican population. Three PLA2G2A gene polymorphisms (rs876018, rs3753827 and rs11573156) were genotyped by 5' exonuclease TaqMan assays in a group of 338 patients with T2DM, 460 individuals with MetS and 366 healthy controls. Under codominant 1(codom1), dominant (dom) and additive (add) models adjusted by age, gender, body mass index (BMI), smoking habit, and hypertension, the rs876018T allele was associated with increased risk of MetS [Odds Ratio (OR)=1.66, P(codom1)=0.005; OR=1.67, P(dom)=0.003; OR=1.49, P(add)=0.005] as compared to controls. On the other hand, under several models adjusted by the same variables, the rs3753827A (OR=1.52, P(codom1)=0.039 and OR=1.49, P(dom)=0.039) and rs11573156C alleles (OR=6.46, P(codom1)=0.013; OR=6.70, P(codom2)=0.009; OR=6.65, P(dom)=0.009) were associated with increased risk of T2DM when compared with controls. In addition, the rs876018T allele was associated with hypercholesterolemia (P(dom)=0.017, P(add)=0.009) and risk of subclinical atherosclerosis (SA) (P(dom)=0.041) in MetS when compared with controls. Also, this allele was associated with SA in T2DM patients (P(dom)=0.007). The TAG haplotype was significantly associated with increased risk of MetS (OR=1.54, P=0.006). Results suggest that PLA2G2A polymorphisms are involved in the risk of developing MetS and T2D and are associated with SA in this group of patients. CI - Copyright (c) 2016 Elsevier GmbH. All rights reserved. FAU - Monroy-Munoz, Irma Eloisa AU - Monroy-Munoz IE AD - Department of Human Genetics and Genomics, Instituto Nacional de Perinatologia Isidro Espinoza de los Reyes, Mexico City, Mexico. FAU - Angeles-Martinez, Javier AU - Angeles-Martinez J AD - Department of Molecular Biology, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico. FAU - Posadas-Sanchez, Rosalinda AU - Posadas-Sanchez R AD - Department of Endocrinology, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico. FAU - Villarreal-Molina, Teresa AU - Villarreal-Molina T AD - Cardiovascular Genomics Laboratory, Instituto Nacional de Medicina Genomica (INMEGEN), Mexico City, Mexico. FAU - Alvarez-Leon, Edith AU - Alvarez-Leon E AD - Department of Molecular Biology, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico. FAU - Flores-Dominguez, Carmina AU - Flores-Dominguez C AD - CICSA, Universidad Anahuac, Mexico. FAU - Cardoso-Saldana, Guillermo AU - Cardoso-Saldana G AD - Department of Endocrinology, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico. FAU - Medina-Urrutia, Aida AU - Medina-Urrutia A AD - Department of Endocrinology, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico. FAU - Juarez-Rojas, Juan Gabriel AU - Juarez-Rojas JG AD - Department of Endocrinology, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico. FAU - Posadas-Romero, Carlos AU - Posadas-Romero C AD - Department of Endocrinology, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico. FAU - Alarcon, Gilberto Vargas AU - Alarcon GV AD - Department of Molecular Biology, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico City, Mexico. Electronic address: gvargas63@yahoo.com. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20160903 PL - Netherlands TA - Immunobiology JT - Immunobiology JID - 8002742 RN - EC 3.1.1.4 (Group II Phospholipases A2) RN - EC 3.1.1.4 (PLA2G2A protein, human) SB - IM MH - Atherosclerosis/*genetics MH - Diabetes Mellitus, Type 2/*genetics MH - Gene Frequency MH - Genetic Association Studies MH - Genetic Predisposition to Disease MH - Genotype MH - Group II Phospholipases A2/*genetics MH - Humans MH - Hypercholesterolemia/*genetics MH - Linkage Disequilibrium MH - Lipogenesis MH - Lipolysis MH - Metabolic Syndrome/*genetics MH - Mexico MH - Polymorphism, Single Nucleotide OTO - NOTNLM OT - Metabolic syndrome OT - Polymorphisms OT - Secretory phospholipase A(2) II A OT - Subclinical atherosclerosis OT - Type 2 diabetes mellitus EDAT- 2016/09/10 06:00 MHDA- 2018/05/01 06:00 CRDT- 2016/09/10 06:00 PHST- 2015/12/16 00:00 [received] PHST- 2016/07/25 00:00 [revised] PHST- 2016/08/30 00:00 [accepted] PHST- 2016/09/10 06:00 [pubmed] PHST- 2018/05/01 06:00 [medline] PHST- 2016/09/10 06:00 [entrez] AID - S0171-2985(16)30361-8 [pii] AID - 10.1016/j.imbio.2016.08.014 [doi] PST - ppublish SO - Immunobiology. 2017 Oct;222(10):967-972. doi: 10.1016/j.imbio.2016.08.014. Epub 2016 Sep 3.