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Associations of objective physical activity with insulin sensitivity and circulating adipokine profile: the Framingham Heart Study

机译:联想客观的体育活动胰岛素敏感性和adipokine传播简介:弗雷明汉心脏研究

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摘要

The purpose of this study was to explore the relation of physical activity (PA) and sedentary time (SED) to insulin sensitivity and adipokines. We assessed PA and SED using Actical accelerometers and insulin resistance (HOMA-IR) in 2109 participants (free of type 1 and 2 diabetes mellitus) from Framingham Generation 3 and Omni 2 cohorts (mean age 46 years, 54% women). Systemic inflammation (C-reactive protein [CRP]) and circulating adipokines were measured 6 years earlier. Steps per day, moderate-to-vigorous PA (MVPA) and SED per wear time (%SED) were predictor variables in multivariabie regression analyses, with HOMA-IR, CRP and circulating adipokines as outcome measures. We reported that higher MVPA and more steps per day were associated with lower HOMA-IR, adjusting for %SED (p = -0.036, P = 0.002; beta = -0.041, beta = 0.005). Steps were inversely associated with CRP, but were directly associated with insulin-like growth factor (IGF)-1 levels (beta = -0.111, P = 0.002; beta = 3.293, P = 0.007). % SED was positively associated with HOMA-IR (beta = 0.033, P < 0.0001), but nonsignificant after adjusting for MVPA (P = 0.13). %SED was associated with higher ratio of leptin/leptin receptor (sOB-R) and higher adipocyte fatty acid-binding protein (FABP)4 (beta = 0.096, P < 0.0001; beta = 0.593, P = 0.002). Our findings suggest differential influences of PA vs. SED on metabolic pathways, with PA modulating insulin resistance and inflammation, whereas SED influences FABPs.
机译:本研究的目的是探索关系的身体活动(PA)和久坐不动的时间(SED)胰岛素敏感性和发病。我们评估了PA和SED使用的选用加速度计和胰岛素抵抗(HOMA-IR)在2109名参与者(类型1和2的自由糖尿病)从弗雷明汉代3和Omni 2组(平均年龄46岁,54%女性)。发病(CRP))和循环测量6年早些时候。每穿到PA (MVPA)和SED时间(% SED)预测变量HOMA-IR multivariabie回归分析,CRP和发病循环的结果措施。步骤降低HOMA-IR,每天调整了% SED (p = -0.036, p = 0.002;-0.041,β= 0.005)。与c反应蛋白有关,但直接相关与胰岛素样生长因子(IGF) 1的水平(β= -0.111,P = 0.002;0.007)。HOMA-IR(β= 0.033,P < 0.0001),但无意义的在调整了MVPA (P =0.13)。瘦素和瘦素受体(sOB-R)和更高脂肪细胞脂肪酸结合蛋白(FABP) 4(β= 0.096,P < 0.0001;0.002)。影响PA和SED的代谢途径,与PA调节胰岛素抵抗和炎症,而SED FABPs影响。

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