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Association between 25-hydroxyvitamin D and inflammatory biomarker levels in a cross-sectional population-based study, Sao Paulo, Brazil

机译:在一项基于人群的横断面研究中,25-羟基维生素D与炎症生物标志物水平之间的关联,巴西圣保罗

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Besides the classic vitamin D function on bone homeostasis, there are bodies of evidence showing that adequate status of vitamin D can modulate inflammation. We hypothesized that higher plasma levels of 25-hydroxyvitamin D (25[OH]D) would correlate with lower plasma levels of proinflammatory cytokines, acute-phase proteins, and soluble adhesion molecules and higher plasma levels of anti-inflammatory cytokines. We included all adults (age, 20-59 years) of the population-based, cross-sectional study, Health Survey-Sao Paulo, conducted in Sao Paulo (Brazil) in the study (n = 281). Anthropometric parameters, blood pressure measurements, and a fasting blood sample were collected by trained fieldworkers. Serum 25(OH)D concentration, plasma inflammatory biomarker levels (C-reactive protein, interleukin [IL]-1 beta, IL-6, IL-8, IL-10, tumor necrosis factor [TNF] alpha, IL-12p70, adiponectin, monocyte chemoattractant protein-1, soluble intercellular adhesion molecule-1, and soluble vascular cell adhesion molecule-1), and plasma blood lipid parameters were evaluated. The prevalence of vitamin D inadequacy (<50 nmol/L) was 65.5%. Inadequate participants were younger, with lower body mass index (BMI), systolic and diastolic blood pressures, triglyceride, and total cholesterol levels as well as low-density lipoprotein cholesterol, compared with individuals adequate for vitamin D status. After adjustment, plasma concentration of soluble intercellular adhesion molecule-1 was statistically higher among adequate participants. Stratifying for BMI categories, a negative association was observed between plasma IL-6 and TNF-alpha levels and serum 25(OH)D concentration in normal-weight participants, whereas a negative association was detected between plasma adiponectin level and serum 25(OH)D concentration in overweight participants. The present findings suggest that BMI interacts with serum 25(OH)D levels, modulating inflammatory response and affecting plasma IL-6, TNF-alpha, and adiponectin levels. These data indicate that BMI plays a determinant role in the vitamin D-inflammation axis. (C) 2016 Elsevier Inc. All rights reserved.
机译:除了经典的维生素D对骨骼稳态的功能外,还有大量证据表明维生素D的适当状态可以调节炎症。我们假设较高的血浆25-羟基维生素D(25 [OH] D)水平将与较低水平的促炎细胞因子,急性期蛋白和可溶性粘附分子血浆水平以及较高水平的抗炎细胞因子相关。在研究中,我们纳入了在巴西圣保罗进行的,以人群为基础的横断面研究(圣保罗健康调查)的所有成年人(20-59岁)(n = 281)。训练有素的现场工作人员收集了人体测量学参数,血压测量值和空腹血样。血清25(OH)D浓度,血浆炎症生物标志物水平(C反应蛋白,白介素[IL] -1 beta,IL-6,IL-8,IL-10,肿瘤坏死因子[TNF]α,IL-12p70,评估了脂联素,单核细胞趋化蛋白-1,可溶性细胞间粘附分子-1和可溶性血管细胞粘附分子-1)以及血浆血脂参数。维生素D不足(<50 nmol / L)的患病率为65.5%。与维生素D状况良好的个体相比,参与者不足,年龄较小,体重指数(BMI),收缩压和舒张压,甘油三酸酯和总胆固醇水平以及低密度脂蛋白胆固醇较低。调整后,在适当的参与者中,可溶性细胞间粘附分子-1的血浆浓度在统计学上较高。按体重指数分类,在正常体重参与者中血浆IL-6和TNF-α水平与血清​​25(OH)D浓度之间呈负相关,而血浆脂联素水平与血清​​25(OH)之间呈负相关。 D超重参与者集中。目前的发现表明,BMI与血清25(OH)D水平相互作用,调节炎症反应并影响血浆IL-6,TNF-α和脂联素水平。这些数据表明,BMI在维生素D-炎症轴中起决定性作用。 (C)2016 Elsevier Inc.保留所有权利。

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