Alleles and haplotypes of the interleukin 10 gene polymorphisms are associated with risk of developing acute coronary syndrome in Mexican patients

被引:24
作者
Manuel Fragoso, Jose [1 ,4 ]
Vallejo, Maite [2 ]
Alvarez-Leon, Edith [1 ]
Delgadillo, Hilda
Antonio Pena-Duque, Marco
Cardoso-Saldana, Guillermo [3 ]
Posadas-Romero, Carlos [3 ]
Antonio Martinez-Rios, Marco
Vargas-Alarcon, Gilberto [1 ]
机构
[1] Inst Nacl Cardiol Ignacio Chavez, Dept Mol Biol, Mexico City, DF, Mexico
[2] Inst Nacl Cardiol Ignacio Chavez, Dept Sociomed, Mexico City, DF, Mexico
[3] Inst Nacl Cardiol Ignacio Chavez, Dept Endocrinol, Mexico City, DF, Mexico
[4] Univ Nacl Autonoma Mexico, Mexico City 04510, DF, Mexico
关键词
Acute coronary syndrome; Genetic susceptibility; Inflammation; Interleukin; 10; Polymorphisms; NECROSIS-FACTOR-ALPHA; GASTRIC-CANCER; MORTALITY; DISEASE; IL-10; TRANSCRIPTION; HEALTH; BLOOD;
D O I
10.1016/j.cyto.2011.03.021
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
Inflammation plays an important role in the pathogenesis of atherosclerosis and acute coronary syndromes (ACS). Interleukin-10 (IL-10) is a potent anti-inflammatory cytokine that mediates the inflammatory process. The objective of the present study was to evaluate the role of IL-10 gene polymorphisms as susceptibility markers for ACS in Mexican patients. IL-10 promoter polymorphisms (positions -1082, -819, and -592) were analyzed by 5' exonuclease TaqMan genotyping assays in 389 ACS patients and 302 healthy controls. ACS patients showed increased frequencies of IL-10-592 C allele and CC genotype when compared to healthy controls (pC = 0.0006, OR = 1.48 and pC = 0.022, OR = 1.56, respectively), whereas the frequencies of the A allele and AA genotype were decreased in patients (pC = 0.0006, OR = 0.68 and pC = 0.006, OR = 0.57, respectively). When the distribution of IL-10-592 genotypes was analyzed separately in women and men (patients and healthy controls), a different distribution of alleles and genotypes was observed only in the group of men. In this case, increased frequency of C allele (pC = 0.004, OR = 1.46) and decreased frequencies of A allele (pC = 0.004, OR = 0.68) and AA genotype (pC = 0.023, OR = 0.56) were observed in the group of patients when compared to healthy controls. Multiple logistic analyses by gender showed that male individuals with IL-10-592 CC + AC genotypes had 3.54-fold increased risk of developing ACS than individuals with AA genotype (p < 0.001). The analysis of linkage disequilibrium showed one (ACC) increased haplotype in patients as compared to healthy controls. The results suggest that IL-10 gene polymorphisms could be involved in the risk of developing ACS in the Mexican population. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:29 / 33
页数:5
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