Interleukin 6 polymorphisms are associated with cardiovascular risk factors in premature coronary artery disease patients and healthy controls of the GEA Mexican study

IF 2.8 4区 医学 Q2 PATHOLOGY Experimental and molecular pathology Pub Date : 2024-02-01 DOI:10.1016/j.yexmp.2024.104886
Rosalinda Posadas-Sánchez , Ángel Rene López-Uribe , José Manuel Fragoso , Gilberto Vargas-Alarcón
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Abstract

Background and aims

Interleukin-6 (IL-6) is an acute-phase protein that plays an important role in the inflammatory response, vascular inflammation, and atherosclerosis process. The study aimed to establish whether IL-6 gene polymorphisms and IL-6 concentrations are associated with premature coronary artery disease (pCAD) and cardiovascular risk factors.

Methods

The IL-6 concentrations and the rs2069827, rs1800796, and rs1800795 IL-6 polymorphisms were determined in 1150 pCAD patients and 1083 healthy controls (coronary artery calcium equal to zero determined by tomography).

Results

The IL-6 polymorphisms studied were not associated with pCAD, but they were associated with cardiovascular risk factors in patients and controls. In controls, under the dominant model, the rs1800795 C allele and the rs2069827 T allele were associated with a low risk of central obesity (OR = 0.401, p = 0.017 and OR = 0.577, p = 0.031, respectively), hypoalphalipoproteinemia (OR = 0.581, p = 0.027 and OR = 0.700, p = 0.014, respectively) and hypertriglyceridemia (OR = 0.575, p = 0.030 and OR = 0.728, p = 0.033, respectively). In pCAD, the rs1800795 C allele was associated with an increased risk of hypoalphalipoproteinemia (OR = 1.370, padditive = 0.025) and increased C-reactive protein (CRP) concentrations (OR = 1.491, padditive = 0.007). pCAD patients had significantly higher serum IL-6 concentrations compared to controls (p = 0.002). In the total population, individuals carrying the rs1800795 GC + CC genotypes had higher levels of IL-6 than carriers of the GG genotype (p = 0.025). In control individuals carrying the C allele (CG + CC), an inverse correlation was observed between IL-6 and HDL-cholesterol levels (p = 0.003).

Conclusions

In summary, the IL-6 polymorphisms were not associated with pCAD, however, they were associated with cardiovascular risk factors in pCAD patients and healthy controls. Individuals carrying the rs1800795 GC + CC genotypes had higher levels of IL-6 than carriers of the GG genotype.

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白细胞介素 6 多态性与墨西哥 GEA 研究中早发冠心病患者和健康对照组的心血管风险因素有关。
背景和目的:白细胞介素-6(IL-6)是一种急性期蛋白,在炎症反应、血管炎症和动脉粥样硬化过程中发挥着重要作用。该研究旨在确定 IL-6 基因多态性和 IL-6 浓度是否与早发性冠状动脉疾病(pCAD)和心血管风险因素相关:方法:测定了 1150 名早发冠状动脉疾病(pCAD)患者和 1083 名健康对照者(通过断层扫描测定冠状动脉钙等于零)的 IL-6 浓度以及 rs2069827、rs1800796 和 rs1800795 IL-6 多态性:所研究的 IL-6 多态性与 pCAD 无关,但与患者和对照组的心血管风险因素有关。在对照组中,在显性模型下,rs1800795 C 等位基因和 rs2069827 T 等位基因与中心性肥胖(OR = 0.401,p = 0.017 和 OR = 0.577,p = 0.031)、低脂蛋白血症(OR = 0.581,p = 0.027 和 OR = 0.700,p = 0.014)和高甘油三酯血症(OR = 0.575,p = 0.030 和 OR = 0.728,p = 0.033)相关。在 pCAD 患者中,rs1800795 C 等位基因与低脑脂蛋白血症风险增加(OR = 1.370,p = 0.025)和 C 反应蛋白(CRP)浓度增加(OR = 1.491,p = 0.007)有关。在整个人群中,携带 rs1800795 GC + CC 基因型的个体的 IL-6 水平高于 GG 基因型携带者(p = 0.025)。在携带 C 等位基因(CG + CC)的对照个体中,观察到 IL-6 与高密度脂蛋白胆固醇水平之间存在反相关性(p = 0.003):总之,IL-6 多态性与 pCAD 无关,但与 pCAD 患者和健康对照组的心血管风险因素有关。与 GG 基因型携带者相比,rs1800795 GC + CC 基因型携带者的 IL-6 水平更高。
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来源期刊
CiteScore
8.90
自引率
0.00%
发文量
78
审稿时长
11.5 weeks
期刊介绍: Under new editorial leadership, Experimental and Molecular Pathology presents original articles on disease processes in relation to structural and biochemical alterations in mammalian tissues and fluids and on the application of newer techniques of molecular biology to problems of pathology in humans and other animals. The journal also publishes selected interpretive synthesis reviews by bench level investigators working at the "cutting edge" of contemporary research in pathology. In addition, special thematic issues present original research reports that unravel some of Nature''s most jealously guarded secrets on the pathologic basis of disease. Research Areas include: Stem cells; Neoangiogenesis; Molecular diagnostics; Polymerase chain reaction; In situ hybridization; DNA sequencing; Cell receptors; Carcinogenesis; Pathobiology of neoplasia; Complex infectious diseases; Transplantation; Cytokines; Flow cytomeric analysis; Inflammation; Cellular injury; Immunology and hypersensitivity; Athersclerosis.
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