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Association of metabolic syndrome with inflammatory markers in a sample of community-dwelling older adults

机译:社区居民老年人样本中代谢综合征与炎症标志物的关联

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The study aimed to identify the cutoff points for inflammatory markers that best discriminate the occurrence of metabolic syndrome in community-dwelling older adults. Baseline data were used from the elderly cohort in the city of Bambuí, Minas Gerais State, Brazil. The target exposure was presence of metabolic syndrome, defined according to the Adult Treatment Panel III criterion, and the outcomes included the following inflammatory markers: cytokines (IL-1β, IL-6, IL-10, IL-12 e TNF), chemokines (CXCL8, CXCL9, CCL2, CXCL10, and CCL5), and C-reactive protein (CRP). Definition of the cutoff points for the inflammatory markers was based on the Classification and Regression Tree (CART) method. The associations between these markers and metabolic syndrome were estimated by logistic regression models, obtaining odds ratios and 95% confidence intervals, considering adjustment for confounding factors. Prevalence of metabolic syndrome was 49.1%, and IL-1β, IL-12, and TNF levels were not associated statistically with this exposure. After adjustment, presence of metabolic syndrome was associated with higher IL-6 and CRP levels and lower CXCL8 and CCL5. Significant associations were also observed with intermediate serum CXCL9 and CXCL10 levels. The combination of markers also showed a significant and consistent association with metabolic syndrome. In addition to demonstrating an association between metabolic syndrome and a wide range of biomarkers (some not previously described in the literature), the results highlight that this association occurs at much lower levels than previously demonstrated, suggesting that metabolic syndrome plays an important role in the inflammatory profile of the older adults.
机译:这项研究旨在确定炎症标志物的临界点,以最佳地区分社区居住的老年人中代谢综合征的发生。基线数据来自巴西米纳斯吉莱斯州Bambuí市的老年人群。目标暴露是根据成人治疗小组III标准定义的代谢综合征的存在,其结果包括以下炎症标志物:细胞因子(IL-1β,IL-6,IL-10,IL-12 e TNF),趋化因子(CXCL8,CXCL9,CCL2,CXCL10和CCL5)和C反应蛋白(CRP)。炎症标志物的临界点的定义基于分类和回归树(CART)方法。这些标志物和代谢综合征之间的关联通过逻辑回归模型进行估计,获得了优势比和95%置信区间,并考虑了对混杂因素的调整。代谢综合征的患病率为49.1%,并且IL-1β,IL-12和TNF水平与该暴露水平在统计学上无关。调整后,代谢综合征的存在与更高的IL-6和CRP水平以及更低的CXCL8和CCL5相关。还观察到与中等血清CXCL9和CXCL10水平的显着关联。标记物的组合还显示出与代谢综合征的显着且一致的关联。除了证明代谢综合征与多种生物标记物之间存在关联(某些文献之前未进行过描述)外,结果还表明该关联发生的水平比以前证明的低得多,这表明代谢综合征在肝癌中起着重要作用。老年人的炎症状况。

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