Association of the suppressor of cytokine signaling 1 (SOCS1) gene polymorphisms with acute coronary syndrome in Mexican patients

被引:7
作者
Vargas-Alarcon, Gilberto [1 ,2 ]
Posadas-Sanchez, Rosalinda [4 ]
Posadas-Romero, Carlos [4 ]
Gonzalez-Salazar, Carmen [4 ]
Cardoso-Saldana, Guillermo [4 ]
Antonio Martinez-Rios, Marco [3 ]
Antonio Pena-Duque, Marco [3 ]
Obil-Chavarria, Claudia [1 ,2 ]
Perez-Mendez, Oscar [1 ,2 ]
Manuel Fragosoa, Jose [1 ,2 ]
机构
[1] Inst Nacl Cardiol Ignacio Chavez, Dept Mol Biol, Mexico City 14080, DF, Mexico
[2] Inst Nacl Cardiol Ignacio Chavez, Intervent Genet Study Grp, Mexico City 14080, DF, Mexico
[3] Inst Nacl Cardiol Ignacio Chavez, Dept Intervent Cardiol, Mexico City 14080, DF, Mexico
[4] Inst Nacl Cardiol Ignacio Chavez, Dept Endocrinol, Mexico City 14080, DF, Mexico
关键词
Acute coronary syndromes; Suppressor of cytokine signaling 1 (SOCS1); Polymorphism; INSULIN-RECEPTOR; PROTEINS; INFLAMMATION; ACTIVATION; BLOOD;
D O I
10.1016/j.molimm.2014.06.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent studies provide evidence on the emerging role of the SOCS1 gene in the development and progression of atherosclerotic lesions. This gene encodes for the suppressor of the cytokine signaling-1 protein that interacts directly with the Janus kinases that are essential intracellular mediators of the immune cytokine action. The aim of this study was to test for associations between SOCS1 gene single nucleotide polymorphisms (SNPs) and the risk of developing acute coronary syndromes (ACS) in a group of Mexicans patients. Four SNPs [-3969 C>T (rs243327), -1656 G>A (rs243330), -820 G>T (rs33977706) and +1125 G>C (rs33932899)] of SOCS1 gene were determined for TaqMan genotyping assays in a group of 447 patients with ACS and 622 healthy controls. Under heterozygous model, the -3969 C>T (rs243327) SNP was associated with increased risk of ACS (OR = 1.45, P-Het = 0.021). On the other hand, under co-dominant and heterozygous models, the -1656 G/A (rs243330) SNP was associated with increased risk of ACS (OR = 1.47, PCo-dom = 0.038 and OR = 1.50, P-Het = 0.013, respectively). Moreover, under co-dominant, dominant, and heterozygous models, the -820T/G (rs33977706) SNP was associated with increased risk of ACS (OR = 1.59, PCo-dom = 0.03, OR= 1.48, P-Dom = 0.028 and OR= 1.61, P-Het = 0.01). Finally, under co-dominant and heterozygous models, the +1125 G/C (rs33932899) SNP was associated with increased risk of ACS (OR= 1.54, PCo-dom = 0.006, OR= 1.58, P-Het = 0.012, respectively). Models were adjusted for gender, age, body index mass, dyslipidemia, alcohol consumption, and smoking. In summary, our data suggests that the four studied polymorphisms of the SOCS1 gene play an important role as susceptibility markers for developing ACS. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:137 / 141
页数:5
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