身体活动和久坐行为与超重成人的组织特异性胰岛素敏感性有明显关联

IF 5.6 2区 医学 Q1 PHYSIOLOGY Acta Physiologica Pub Date : 2023-02-06 DOI:10.1111/apha.13945
Lisa Wanders, Anouk Gijbels, Esmée A. Bakker, Inez Trouwborst, Kelly M. Jardon, Koen C. M. Manusama, Gabby B. Hul, Edith J. M. Feskens, Lydia A. Afman, Ellen E. Blaak, Maria T. E. Hopman, Gijs H. Goossens, Dick H. J. Thijssen
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引用次数: 3

摘要

目的本研究的目的是探讨身体活动(PA)谱(久坐行为到运动)与组织特异性胰岛素抵抗(IR)之间的关系。方法纳入219名受试者进行分析(中位数[IQR]: 61 [55;67岁,BMI 29.6 [26.9;32.0 kg / m2);60%为女性),以肌肉或肝脏IR为主,通过7点口服葡萄糖耐量试验(OGTT)确定。在7天内客观测量PA和久坐行为(ActivPAL)。使用Baecke问卷评估情境特异性PA。采用多元线性回归模型(调整包括年龄、性别、BMI、地点、季节、退休和饮食摄入)来确定PA谱与肝脏胰岛素抵抗指数(HIRI)、肌肉胰岛素敏感性指数(MISI)和全身IR (HOMA-IR、Matsuda指数)之间的关系。结果在完全调整后的模型中,客观测量的总PA(标准化回归系数β = 0.17, p = 0.020)、轻强度PA (β = 0.15, p = 0.045)和中高强度PA (β = 0.13, p = 0.048)与Matsuda指数独立相关,但与HOMA-IR无关(p > 0.05)。较高的问卷调查衍生的运动指数和休闲指数与男性显著较低的全身IR (Matsuda, HOMA-IR)相关,但与女性无关。不同组织的结果不同:久坐时间越长(β = - 0.24, p = 0.045)和休闲指数越高(β = 0.14, p = 0.034)分别与MISI呈负相关和正相关,但与HIRI无关。较高的运动指数与较低的HIRI相关(β = - 0.30, p = 0.007,仅在男性中)。结论:虽然我们证实了PA与全身IR之间的有益关联,但我们的研究结果表明,PA谱与IR之间的关联似乎因胰岛素抵抗的原发部位(肌肉或肝脏)而异。
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Physical activity and sedentary behavior show distinct associations with tissue-specific insulin sensitivity in adults with overweight

Aim

The aim of this study is to investigate associations between the physical activity (PA) spectrum (sedentary behavior to exercise) and tissue-specific insulin resistance (IR).

Methods

We included 219 participants for analysis (median [IQR]: 61 [55; 67] years, BMI 29.6 [26.9; 32.0] kg/m2; 60% female) with predominant muscle or liver IR, as determined using a 7-point oral glucose tolerance test (OGTT). PA and sedentary behavior were measured objectively (ActivPAL) across 7 days. Context-specific PA was assessed with the Baecke questionnaire. Multiple linear regression models (adjustments include age, sex, BMI, site, season, retirement, and dietary intake) were used to determine associations between the PA spectrum and hepatic insulin resistance index (HIRI), muscle insulin sensitivity index (MISI) and whole-body IR (HOMA-IR, Matsuda index).

Results

In fully adjusted models, objectively measured total PA (standardized regression coefficient β = 0.17, p = 0.020), light-intensity PA (β = 0.15, p = 0.045) and moderate-to-vigorous intensity PA (β = 0.13, p = 0.048) were independently associated with Matsuda index, but not HOMA-IR (p > 0.05). A higher questionnaire-derived sport index and leisure index were associated with significantly lower whole-body IR (Matsuda, HOMA-IR) in men but not in women. Results varied across tissues: more time spent sedentary (β = −0.24, p = 0.045) and a higher leisure index (β = 0.14, p = 0.034) were respectively negatively and positively associated with MISI, but not HIRI. A higher sport index was associated with lower HIRI (β = −0.30, p = 0.007, in men only).

Conclusion

While we confirm a beneficial association between PA and whole-body IR, our findings indicate that associations between the PA spectrum and IR seem distinct depending on the primary site of insulin resistance (muscle or liver).

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来源期刊
Acta Physiologica
Acta Physiologica 医学-生理学
CiteScore
11.80
自引率
15.90%
发文量
182
审稿时长
4-8 weeks
期刊介绍: Acta Physiologica is an important forum for the publication of high quality original research in physiology and related areas by authors from all over the world. Acta Physiologica is a leading journal in human/translational physiology while promoting all aspects of the science of physiology. The journal publishes full length original articles on important new observations as well as reviews and commentaries.
期刊最新文献
Correction to "Beneficial effects of MGL-3196 and BAM15 combination in a mouse model of fatty liver disease". Issue Information Impaired suppression of fatty acid release by insulin is a strong predictor of reduced whole-body insulin-mediated glucose uptake and skeletal muscle insulin receptor activation. Differential production of mitochondrial reactive oxygen species between mouse (Mus musculus) and crucian carp (Carassius carassius) A quantitative analysis of bestrophin 1 cellular localization in mouse cerebral cortex.
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