The HIF1A rs2057482 polymorphism is associated with risk of developing premature coronary artery disease and with some metabolic and cardiovascular risk factors. The Genetics of Atherosclerotic Disease (GEA) Mexican Study

被引:21
作者
Lopez-Reyes, Alberto [1 ]
Manuel Rodriguez-Perez, Jose [2 ]
Fernandez-Torres, Javier [1 ]
Martinez-Rodriguez, Nancy [2 ]
Perez-Hernandez, Nonanzit [2 ]
Javier Fuentes-Gomez, Arturo [1 ]
Alberto Aguilar-Gonzalez, Carlos [1 ]
Alvarez-Leon, Edith [2 ]
Posadas-Romero, Carlos [3 ]
Villarreal-Molina, Teresa [4 ]
Pineda, Carlos [1 ]
Vargas-Alarcon, Gilberto [2 ]
机构
[1] Inst Natl Rehabil, Mol Synovioanal Lab, Mexico City, DF, Mexico
[2] Inst Nacl Cardiol Ignacio Chavez, Dept Mol Biol, Mexico City 14080, DF, Mexico
[3] Inst Nacl Cardiol Ignacio Chavez, Dept Endocrinol, Mexico City 14080, DF, Mexico
[4] Inst Natl Med Genorn, Genom Lab, Mexico City, DF, Mexico
关键词
Cardiovascular risk factors; Coronary artery disease; Hypoxia; Hypoxia-inducible factor 1-alpha; lschemia; Polymorphisms; HYPOXIA-INDUCIBLE FACTOR-1-ALPHA; COMPUTED-TOMOGRAPHY; EXPRESSION; CANCER; HIF-1-ALPHA;
D O I
10.1016/j.yexmp.2014.04.010
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The aim of the present study was to establish the role of HIF1A gene polymorphisms in the risk of developing premature coronary artery disease (CAD) in a well-characterized clinical cohort. Three polymorphisms in HIF1A (rs11549465, rs11549467, rs2057482) gene were genotyped in 949 patients with premature CAD, and 676 healthy controls (with negative calcium score by computed tomography). Under a dominant model adjusted for age, visceral to subcutaneous adipose tissue (VAT/SAT) ratio, hypertension, type 2 diabetes mellitus (T2DM), HDL-C levels, hypercholesterolemia and hypertriglyceridemia, the rs2057482 T allele was associated with decreased risk of premature CAD when compared to healthy controls (OR = 0.616, P-dom = 0.020). The effect of the studied polymorphisms on various metabolic parameters and cardiovascular risk factors was explored. In this analysis, the rs2057482 T allele was associated with decreased risk of obesity, central obesity, hypertension, hypercholesterolemia, hypertriglyceridemia and increased risk of T2DM. Under a dominant model adjusted by age, the HIF1A rs2057482 T polymorphism was associated with high VAT/SAT ratio (P = 0.009) and HDL-C levels (P = 0.04) in healthy controls. The results suggest that HIF1A rs2057482 polymorphism is involved in the risk of developing CAD and is associated with some metabolic parameters and cardiovascular risk factors. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:405 / 410
页数:6
相关论文
共 42 条
[31]   Interactions between rs5498 polymorphism in the ICAM1 gene and traditional risk factors influence susceptibility to coronary artery disease [J].
Sarecka-Hujar, Beata ;
Zak, Iwona ;
Krauze, Jolanta .
CLINICAL AND EXPERIMENTAL MEDICINE, 2009, 9 (02) :117-124
[32]   The-930A>G polymorphism of the CYBA gene is associated with premature coronary artery disease. A case-control study and gene-risk factors interactions [J].
Niemiec, Pawel ;
Nowak, Tomasz ;
Iwanicki, Tomasz ;
Krauze, Jolanta ;
Gorczynska-Kosiorz, Sylwia ;
Grzeszczak, Wladyslaw ;
Ochalska-Tyka, Anna ;
Zak, Iwona .
MOLECULAR BIOLOGY REPORTS, 2014, 41 (05) :3287-3294
[33]   Heterozygosity in LDLR rs2228671 and rs72658855 Gene is Associated with Increased Risk of Developing Coronary Artery Disease in India -A Case-Control Study [J].
Jha, Chandan K. ;
Mir, Rashid ;
Banu, Shaheena ;
Elfaki, Imadeldin ;
Chahal, Sukh M. S. .
ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS, 2020, 20 (03) :388-399
[34]   Positive Association of theJAG1rs1327235 Genotype with Coronary Artery Disease in Men, the Tampere Adult Population Cardiovascular Risk Study [J].
Kunnas, Tarja ;
Nikkari, Seppo T. .
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2020, 24 (10) :681-684
[35]   Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: The Athero Gene Study [J].
Kallel, Choumous ;
Cohen, William ;
Saut, Noemie ;
Blankenberg, Stefan ;
Schnabel, Renate ;
Rupprecht, Hans J. ;
Bickel, Christoph ;
Munzel, Thomas ;
Tregouet, David-Alexandre ;
Morange, Pierre-Emmanuel .
BMC MEDICAL GENETICS, 2012, 13
[36]   The rs5888 single nucleotide polymorphism in scavenger receptor class B type 1 (SCARB1) gene and the risk of premature coronary artery disease: a case-control study [J].
Goodarzynejad, Hamidreza ;
Boroumand, Mohammadali ;
Behmanesh, Mehrdad ;
Ziaee, Shayan ;
Jalali, Arash .
LIPIDS IN HEALTH AND DISEASE, 2016, 15
[37]   The rs5888 single nucleotide polymorphism in scavenger receptor class B type 1 (SCARB1) gene and the risk of premature coronary artery disease: a case-control study [J].
Hamidreza Goodarzynejad ;
Mohammadali Boroumand ;
Mehrdad Behmanesh ;
Shayan Ziaee ;
Arash Jalali .
Lipids in Health and Disease, 15
[38]   Lectin-Like OLR1 3′UTR Rs1050286 Gene Polymorphism and Plasma Oxidized-LDL in Coronary Artery Disease and Their Relation to Cardiovascular Risk and Outcomes [J].
Mohammed, Hanan Sharaf El-Deen ;
Kamal, Manal Mohamed ;
ElBadre, Hala Mostafa ;
Hosni, Amal ;
Elfadl, Azza Abo ;
Mostafa, Mohamed Ahmed ;
El-Mandy, Reham Ibrahim .
REPORTS OF BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2022, 10 (04) :537-553
[39]   The UCP2-866G/A, Ala55Val and UCP3-55C/T polymorphisms are associated with premature coronary artery disease and cardiovascular risk factors in Mexican population [J].
Gamboa, Ricardo ;
Huesca-Gomez, Claudia ;
Lopez-Perez, Vanessa ;
Posadas-Sanchez, Rosalinda ;
Cardoso-Saldana, Guillermo ;
Medina-Urrutia, Aida ;
Gabriel Juarez-Rojas, Juan ;
Elena Soto, Maria ;
Posadas-Romero, Carlos ;
Vargas-Alarcon, Gilberto .
GENETICS AND MOLECULAR BIOLOGY, 2018, 41 (02) :371-378
[40]   Scavenger Receptor Class B Type 1 Gene rs5888 Single Nucleotide Polymorphism and the Risk of Coronary Artery Disease and Ischemic Stroke: A Case-Control Study [J].
Wu, Dong-Feng ;
Yin, Rui-Xing ;
Cao, Xiao-Li ;
Chen, Wu-Xian ;
Aung, Lynn Htet Htet ;
Wang, Wei ;
Huang, Ke-Ke ;
Huang, Ping ;
Zeng, Xiao-Na ;
Wu, Jian .
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, 2013, 10 (12) :1771-1777