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Constitutive DPP4 activity, inflammation, and microvascular reactivity in subjects with excess body weight and without diabetes

机译:组成型DPP4活性,炎症和微血管反应性,体重过剩和没有糖尿病

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ObjectiveIn patients with diabetes, dipeptidyl peptidase 4 (DPP4) inhibition is associated with attenuation of inflammation and endothelial dysfunction. Here, we investigated the associations between constitutive DPP4 activity, inflammatory biomarkers, and microvascular reactivity in subjects with excess body weight without diabetes. MethodsForty subjects of BMI?≥?25.0?kg/m2and without diabetes were cross-sectionally evaluated. We assessed microvascular blood flow and vasomotion by laser Doppler flowmetry, and measured at baseline, 30, and 60?min after a standardized meal: DPP4 activity, glucose, insulin, hs-CRP, TNF-α, IL-6, PAI-1, ICAM-1, and VCAM-1. HOMA-IR and HOMA-AD were used to assess insulin resistance. Linear correlations of DPP4 activity with the biomarkers of inflammation and components of microvascular function were conducted. In step further, multiple regression analyses were performed to test whether some of these variables could influence, or be influenced by, the plasma DPP4 activity. ResultsDPP4 activity was inversely associated with VCAM-1 at baseline (P?
机译:目的肢体糖尿病患者,二肽基肽酶4(DPP4)抑制与炎症和内皮功能障碍的衰减有关。在这里,我们调查了组成型DPP4活性,炎症生物标志物和在没有糖尿病的体重过剩的受试者中的微血管反应性之间的关联。方法BMI的悲伤患者≥?25.0?kg / m2,没有糖尿病的kg / m2。通过激光多普勒流动性评估微血管血流和血管血管血管血管血管血管血管血管血管血流量,并在标准化膳食后在基线,30和60℃下测量:DPP4活性,葡萄糖,胰岛素,HS-CRP,TNF-α,IL-6,PAI-1 ,ICAM-1和VCAM-1。 HOMA-IR和HOMA-AD用于评估胰岛素抵抗力。进行了DPP4活性与炎症生物标志物的线性相关性和微血管功能组分。在步骤进一步中,进行多元回归分析以测试这些变量中的一些是否可以影响等离子体DPP4活性的影响或受影响。结果DDPP4活性与基线VCAM-1与VCAM-1相关联(P?<β05),DPP4 activityAucwas与肌菌培养件血管定向逆转(P?<β05)。在多元回归分析中,HOMA-AD,IL-6,VCAM-1,PAI-1,血流和血管定律影响了DPP4的活动,并解释了近40%的差异。当分别作为依赖变量置于依赖变量的HOMA-AD,VCAM-1和血液时,DPP4活性在所有这些中发出了显着的影响。结论结论是DPP4活性与内皮促炎症激活和微血管功能的早期标志物相关,并且可能产生影响,甚至受到没有糖尿病的过剩体重的受试者的炎症和微血管血流的影响。

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