跳至主要内容
临床试验/NCT04007926
NCT04007926暂停不适用

Effects of Exercise Training on Insulin Sensitivity in South Asians at Risk of Diabetes: the Roles of Skeletal Muscle Microvasculature and Mitochondrial Metabolism

University of Glasgow2 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2021年8月最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
入组人数
66
试验地点
2
主要终点
Whole-body Insulin sensitivity

研究概览

简要总结

This study determines the effect of aerobic and resistance exercise training on whole-body and skeletal muscle insulin sensitivity in south Asians and evaluate the mechanisms which contribute to improvements in insulin sensitivity after exercise training.

详细描述

South Asians (SA) have 2-4 fold higher risk of type 2 diabetes and develop the disease at lower body weights and younger ages than white Europeans. Lower cardiorespiratory fitness and capacity for muscle fat oxidation contributes substantially to SAs' greater insulin resistance, the extent to which this can be improved by exercise training is unclear. This randomised controlled trial will investigate the effects of a 12-week aerobic or resistance exercise training intervention on insulin sensitivity (hyperinsulinaemic-euglycaemic clamp) in South Asian adults (22 control, 22 aerobic exercise group and 22 resistance exercise group). The study will also explore the mechanisms within skeletal muscle which mediate these changes by evaluating aerobic and resistance exercise-training induced changes: in basal and insulin-stimulated microvascular blood volume (using contrast-enhanced ultrasound); skeletal muscle mitochondrial function; and lipid droplet morphology and spatial interaction with mitochrondria, muscle fibre capillarisation, endothelial content of key enzymes controlling dilation/constriction and GLUT-4 translocation (using confocal immunofluorescence microscopy and transmission electron microscopy methods). Thus, this work will integrate physiological and molecular data to determine the extent to which exercise training can improve insulin sensitivity in SA and the mechanisms underpinning this improvement. This knowledge is important for optimising diabetes prevention interventions in SAs and identification of potential novel therapeutic targets.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

盲法说明

Masking is not possible due to nature of intervention (exercise training programme).

入排标准

年龄范围
30 Years 至 65 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • South Asian ethnicity (self-report of both parents of Indian, Pakistani, Bangladeshi or Sri Lankan origin)
  • Age 30-65 years
  • At least 10% 10-year risk of developing type 2 diabetes, determined using the QDiabetes®2018 risk score (http://qdiabetes.org/2018/index.php)

排除标准

  • Diabetes (physician diagnosed or HbA1c ≥48 mmol/mol on screening)
  • History of cardiovascular disease
  • Hypertension (taking anti-hypertensives or BP consistently ≥ 150/90 mmHg on screening).
  • Regular participation in vigorous physical activity
  • Regular participation in resistance exercise
  • Current smoking
  • Taking drugs or supplements thought to affect carbohydrate or lipid metabolism
  • Taking drugs affecting blood clotting (e.g. aspirin)
  • Current treatment with anti-obesity drugs
  • Any other significant illness that would prevent full participation in the study

结局指标

主要结局

Whole-body Insulin sensitivity

时间窗: Change between baseline and 12 weeks.

Change in whole-body insulin sensitivity measured by hyperinsulinaemic-euglycaemic clamp.

次要结局

  • Insulin-stimulated GLUT4 translocation(Change between baseline and 12 weeks.)
  • Microvascular blood volume(Change between baseline and 12 weeks.)
  • Muscle mitochondrial function(Change between baseline and 12 weeks.)
  • Lipid droplet content in skeletal muscle(Change between baseline and 12 weeks.)
  • Lipid droplet proximity to mitochondria in skeletal muscle(Change between baseline and 12 weeks.)
  • Microvascular density in skeletal muscle(Change between baseline and 12 weeks.)
  • Change in enzymes controlling insulin-mediated increases in perfusion in skeletal muscle(Change between baseline and 12 weeks.)
  • Maximal oxygen uptake(Change between baseline and 12 weeks.)
  • Muscle maximal voluntary contraction(Change between baseline and 12 weeks.)
  • Lower body muscle strength(Change between baseline and 12 weeks.)
  • Upper body muscle strength(Change between baseline and 12 weeks.)
  • Grip strength(Change between baseline and 12 weeks.)
  • Weight(Change between baseline and 12 weeks.)
  • Waist circumference(Change between baseline and 12 weeks.)
  • Fat mass(Change between baseline and 12 weeks.)
  • Fat-free mass(Change between baseline and 12 weeks.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Professor Jason Gill

Professor

University of Glasgow

研究点 (2)

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