Núcleo de Pesquisa em Ciências Biológicas, Programa de Pós-Graduação em Ciências Biológicas, Instituto de Ciências Exatas e Biológicas, Universidade Federal de Ouro Preto, Ouro Preto, MG, Brasil.
Laboratório de Epidemiologia, Departamento de Medicina de Família, Saúde Mental e Coletiva, Escola de Medicina, Universidade Federal de Ouro Preto, Ouro Preto, MG, Brasil.
Braz J Med Biol Res. 2020;53(6):e9113. doi: 10.1590/1414-431x20209113. Epub 2020 May 8.
Chemerin is an adipokine that has been associated with components of metabolic syndrome. It has been described to affect adipocyte metabolism and inflammatory responses in adipose tissue, as well as the systemic metabolism of lipids and glucose. Few epidemiological studies have evaluated classical and genetics cardiovascular risk factors (CVRFs) in the mixed adult rural population in Brazil. Therefore, the present study explored possible associations between CVRFs and chemerin. This cross-sectional study included 508 adults from the rural localities of Lavras Novas, Chapada, and Santo Antônio do Salto in Ouro Preto, Minas Gerais, Southeast Brazil. Demographic, behavioral, clinical, biochemical, anthropometric variables, and 12 single nucleotide polymorphisms (SNPs) linked with metabolic syndrome phenotypes were evaluated for associations with chemerin level. There was a significant association of high triglyceride levels [odds ratio (OR)=1.91, 95%CI: 1.23-2.98], insulin resistance (OR=1.82, 95%CI: 1.03-3.22), age (OR=1.64, 95%CI: 1.08-2.49), and sex (OR=1.99, 95%CI: 1.35-2.95) with high levels of chemerin. High chemerin levels were significantly associated with the genetic polymorphisms rs693 in the APOB gene (OR=1.50, 95%CI: 1.03-2.19) and rs1799983 in the NOS3 gene (OR=1.46, 95%CI: 1.01-2.12) for the AA and GT+TT genotypes, respectively. In the concomitant presence of genotypes AA of rs693 and GT+TT of rs1799983, the chance of presenting high levels of chemerin showed a 2.21-fold increase (95%CI: 1.25-3.88) compared to the reference genotype. The development of classical CVRFs in this population may be influenced by chemerin and by two risk genotypes characteristic of variants in well-studied genes for hypertension and dyslipidemia.
趋化素是一种脂肪因子,与代谢综合征的成分有关。它被描述为影响脂肪组织中脂肪细胞的代谢和炎症反应,以及脂质和葡萄糖的全身代谢。很少有流行病学研究评估巴西混合成年农村人口的经典和遗传心血管危险因素 (CVRFs)。因此,本研究探讨了 CVRFs 与趋化素之间的可能关联。这项横断面研究包括来自巴西东南部米纳斯吉拉斯州奥罗普雷托的拉夫拉斯诺瓦斯、查帕达和圣安东尼奥·多·萨尔托农村地区的 508 名成年人。评估了人口统计学、行为、临床、生化、人体测量学变量和与代谢综合征表型相关的 12 个单核苷酸多态性 (SNP) 与趋化素水平的关联。高水平的甘油三酯 [比值比 (OR)=1.91,95%可信区间:1.23-2.98]、胰岛素抵抗 (OR=1.82,95%可信区间:1.03-3.22)、年龄 (OR=1.64,95%可信区间:1.08-2.49) 和性别 (OR=1.99,95%可信区间:1.35-2.95) 与高水平的趋化素有显著关联。高水平的趋化素与 APOB 基因中的 rs693 多态性 (OR=1.50,95%可信区间:1.03-2.19) 和 NOS3 基因中的 rs1799983 多态性 (OR=1.46,95%可信区间:1.01-2.12) 的 AA 和 GT+TT 基因型显著相关。在 rs693 的 AA 基因型和 rs1799983 的 GT+TT 基因型同时存在的情况下,与参考基因型相比,出现高水平趋化素的可能性增加了 2.21 倍 (95%可信区间:1.25-3.88)。该人群中经典 CVRFs 的发展可能受趋化素和两种风险基因型的影响,这两种风险基因型是高血压和血脂异常的研究充分的基因中的变异特征。