与中强度连续训练相比,低量高强度间歇训练对2型糖尿病女性炎症的影响

A. Marcotte-Chénard, Renaud Tremblay, M. Mony, D. Tremblay, P. Boulay, M. Brochu, J. Morais, I. Dionne, M. Langlois, W. Mampuya, D. Tessier, E. Riesco
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摘要

背景:目的是比较低容量高强度间歇训练(HIIT)和中等强度连续训练(MICT)对老年2型糖尿病(T2D)女性炎症的影响。方法:30名老年无运动的T2D女性(68±5岁)随机分为两组:HIIT(75分钟/周,高强度10分钟/次)和MICT(150分钟/周)。炎症谱(IL-6、IL-10、IL-15、TNF- α和MCP-1;在干预3个月前后的空腹状态下测量27名参与者的Luminex、体成分(iDXA)和心脏代谢谱(A1c、葡萄糖、胰岛素、血脂)。结果:MICT组空腹细胞因子水平保持不变(p≥0.18),HIIT组循环MCP-1水平升高(从160.9 [IQR: 133.5-230.2]增加到187.88 [155.3-237.3])(p = 0.023)。线性回归显示MCP-1浓度的变化与A1c的变化呈正相关(校正r2 = 0.203;P = 0.018)。结论:本研究的结果表明,12周的低容量HIIT或MICT并不能改善老年不适t2dm女性的炎症标志物。A1c和MCP-1水平变化之间的相关性支持高血糖在低度炎症中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Low-Volume High-Intensity Interval Training Compared to Moderate-Intensity Continuous Training on Inflammatory Profile in Women with Type 2 Diabetes
Background : The objective was to compare the effects of low-volume high-intensity interval training (HIIT) to moderate-intensity continuous training (MICT) on the inflammatory profile in older women with type 2 diabetes (T2D). Methods : Thirty older physically inactive women (68 ± 5 years) with T2D were randomized in two groups: HIIT (75 min/week with 10 min/session at high intensity) or MICT (150 min/week). Inflammatory profile (IL-6, IL-10, IL-15, TNF- α , and MCP-1; Luminex), body composition (iDXA), and cardiometabolic profile (A1c, glucose, insulin, lipids) were measured in fasting state, before and after the 3-month intervention in 27 participants. Results : While fasting levels of cytokines remained unchanged in the MICT group ( p ≥ 0.18), circulating MCP-1 levels increased (from 160.9 [IQR: 133.5–230.2] to 187.88 [155.3–237.3]) in the HIIT group ( p = 0.023). Linear regression revealed that changes in MCP-1 concentrations were positively associated with changes in A1c ( adjusted R 2 = 0.203; p = 0.018). Conclusions : The results of this study suggest that 12 weeks of either low-volume HIIT or MICT do not improve inflammatory markers in older unfit women with T2D. The correlation between changes in A1c and MCP-1 levels support the role of hyperglycemia in low-grade inflammation.
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