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Plasma visfatin concentrations after a lifestyle intervention were directly associated with inflammatory markers.

机译:生活方式干预后血浆visfatin浓度与炎症标志物直接相关。

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BACKGROUND AND AIMS: The biological activity and regulation of the novel adipokine visfatin are still largely unknown. Our aim was to evaluate if visfatin plasma concentrations may be influenced by a lifestyle intervention. METHODS AND RESULTS: Out of 335 dysmetabolic patients from a population-based cohort, randomized to receive a lifestyle intervention program (intervention group) or family physician usual care (controls), 20 patients per group were randomly selected for plasma visfatin determination. The before-after variation (Delta) in visfatin concentration at 1-year from randomization, and the correlations between (Delta)visfatin and intervention-induced changes in waist circumference, fasting glucose, markers of inflammation, and oxidative stress were evaluated. The intervention group showed a significant improvement in waist circumference, and many metabolic/inflammatory variables, while the controls worsened. Visfatin concentrations slightly decreased in the former and significantly increased in the controls ((Delta)visfatin=-2.4 vs 66.0 ng/ml, p<0.001). In robust regression models, the following variables resulted associated with (Delta)visfatin: (Delta)waist circumference, (Delta)fasting glucose, (Delta)hs-CRP (high-sensitivity C-reactive protein) and (Delta)TNFalpha (tumor necrosis factor-alpha). Significant effects on (Delta)visfatin of (Delta)TNFalpha (beta=16.8; 6.1-25.6; p=0.003) and, modified by group, of (Delta)hs-CRP (beta=29.8; 95% CI 15.4-44.2; p<0.001 and beta=4.2; 2.9-5.5; p<0.001 in the control and intervention group, respectively) were detected. By controlling for (Delta)waist, the effects of (Delta)TNFalpha and of (Delta)hs-CRP on (Delta)visfatin by group did not change, while (Delta)waist was no longer associated. The association between (Delta)visfatin and (Delta)glucose was no longer significant, after adjusting for (Delta)hs-CRP. CONCLUSION: Visfatin values increased with waist circumference and were associated with variations of inflammatory markers, suggesting participation in inflammatory mechanisms.
机译:背景与目的:新型脂肪己酮visfatin的生物学活性和调控尚不清楚。我们的目的是评估visfatin血浆浓度是否可能受到生活方式干预的影响。方法和结果:在来自以人群为基础的队列的335名代谢不良患者中,随机接受生活方式干预计划(干预组)或家庭医生常规护理(对照),每组随机选择20名患者进行血浆visfatin测定。评估随机分组后1年时visfatin浓度的前后变化(Δ),以及Δvisfatin与干预引起的腰围,空腹血糖,炎症标志物和氧化应激变化之间的相关性。干预组显示腰围明显改善,并且许多代谢/炎症变量增加,而对照组则恶化。 Visfatin浓度在前者中略有降低,而在对照中则显着增加(Δvisfatin= -2.4对66.0 ng / ml,p <0.001)。在稳健的回归模型中,以下变量与Δvisfatin有关:Δ腰围,Δ空腹血糖,Δhs-CRP(高敏C反应蛋白)和ΔTNFα(肿瘤坏死因子-α)。对ΔTNFα(β= 16.8; 6.1-25.6; p = 0.003)和对Δhs-CRP(β= 29.8; 95%CI 15.4-44.2;在对照组和干预组中分别检测到p <0.001和beta = 4.2; 2.9-5.5; p <0.001)。通过控制Δ腰,按组,ΔTNFα和Δhs-CRP对Δvisfatin的作用没有改变,而Δ腰不再相关。调整Δhs-CRP后,Δvisfatin和Δ葡萄糖之间的关联不再显着。结论:Visfatin值随腰围的增加而增加,并与炎症标志物的变化有关,提示其参与了炎症机制。

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