Mechanisms of Insulin Resistance and Exercise in South Asians

October 7, 2020 updated by: Professor Jason Gill, University of Glasgow

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

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.

Study Overview

Detailed Description

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.

Study Type

Interventional

Enrollment (Anticipated)

66

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Glasgow, United Kingdom, G12 8QQ
        • University of Glasgow

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

30 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Male
  • 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)

Exclusion Criteria:

  • Female
  • 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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control Group
Participants assigned to the control arm of the study will be asked to maintain their normal dietary and exercise habits.
Experimental: Aerobic exercise group
Participants randomised to the aerobic exercise intervention will undertake a 12-week aerobic exercise training programme.
Participants will start with 3 x 20 minute exercise sessions in the first week, building up to 5 x 60 minutes of exercise by weeks 9-12 of the intervention, at an intensity of 65-80% of predicted maximum heart rate.
Experimental: Resistance exercise group
Participants randomised to the resistance exercise intervention will undertake a 12-week aerobic exercise training programme.
Participants will undertake two supervised sessions per week. The exercises performed during each session will consist of leg press, calf press, leg extension, leg curl, chest press, shoulder press, lateral pull down and seated row. Exercises will be performed at 60-80% 1RM. In weeks 1-2 participants will perform, during each session, a single set of 5-10 repetitions of each exercise (tiring but comfortably achievable) to ensure they are comfortable with the exercises and are performing these in the correct form. In weeks 3-4 participants will perform, during each session, two sets of each exercise to voluntary muscular failure - defined as not being able to perform single another repetition. In weeks 5-12 this will progress to 3 sets of each exercise to voluntary muscular failure, in each session.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Whole-body Insulin sensitivity
Time Frame: Change between baseline and 12 weeks.
Change in whole-body insulin sensitivity measured by hyperinsulinaemic-euglycaemic clamp.
Change between baseline and 12 weeks.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Insulin-stimulated GLUT4 translocation
Time Frame: Change between baseline and 12 weeks.
Change in insulin-stimulated GLUT4 translocation in muscle biopsies from vastus lateralis using immunofluorescence microscopy
Change between baseline and 12 weeks.
Microvascular blood volume
Time Frame: Change between baseline and 12 weeks.
Change in fold-increase in insulin stimulated quadriceps muscle blood volume measured using contrast enhanced ultrasound.
Change between baseline and 12 weeks.
Muscle mitochondrial function
Time Frame: Change between baseline and 12 weeks.
Change in mitochondrial function (oxygen consumption rate) in isolated skeletal muscle mitochondria from the vastus lateralis measured using respirometry
Change between baseline and 12 weeks.
Lipid droplet content in skeletal muscle
Time Frame: Change between baseline and 12 weeks.
Change in fibre type-specific (type 1 and type 2) and subcellular-specific (subsarcolemmal and intermyofibrillar) lipid droplet content in muscle biopsies from vastus lateralis using immunofluorescence microscopy
Change between baseline and 12 weeks.
Lipid droplet proximity to mitochondria in skeletal muscle
Time Frame: Change between baseline and 12 weeks.
Change in proportion of lipid droplets in contact with mitochondria in subsarcolemmal and intermyofibrillar compartments of type 1 and type 2 muscle fibres in muscle biopsies from vastus lateralis using immunofluorescence microscopy
Change between baseline and 12 weeks.
Microvascular density in skeletal muscle
Time Frame: Change between baseline and 12 weeks.
Change in fibre-type specific capillarisation in muscle biopsies from vastus lateralis
Change between baseline and 12 weeks.
Change in enzymes controlling insulin-mediated increases in perfusion in skeletal muscle
Time Frame: Change between baseline and 12 weeks.
Change in endothelial specific protein content and phosphorylation of key microvascular enzymes in muscle biopsies from vastus lateralis assessed using quantitative immunofluorescence.
Change between baseline and 12 weeks.
Maximal oxygen uptake
Time Frame: Change between baseline and 12 weeks.
Change in maximal oxygen uptake consumption assessed using continuous incremental uphill walking protocol until volitional exhaustion.
Change between baseline and 12 weeks.
Muscle maximal voluntary contraction
Time Frame: Change between baseline and 12 weeks.
Change in knee extensor muscles maximal voluntary contraction
Change between baseline and 12 weeks.
Lower body muscle strength
Time Frame: Change between baseline and 12 weeks.
Change in 1-RM (one maximal repetition) (kg) for leg press.
Change between baseline and 12 weeks.
Upper body muscle strength
Time Frame: Change between baseline and 12 weeks.
Change in 1-RM (one maximal repetition) (kg) for chest press.
Change between baseline and 12 weeks.
Grip strength
Time Frame: Change between baseline and 12 weeks.
Change in grip strength (kg).
Change between baseline and 12 weeks.
Fat mass
Time Frame: Change between baseline and 12 weeks.
Change in fat mass measured with bioelectrical impedance analysis (BIA).
Change between baseline and 12 weeks.
Fat-free mass
Time Frame: Change between baseline and 12 weeks.
Change in fat-free mass measured with bioelectrical impedance analysis (BIA).
Change between baseline and 12 weeks.
Weight
Time Frame: Change between baseline and 12 weeks.
Change in weight (kg).
Change between baseline and 12 weeks.
Waist circumference
Time Frame: Change between baseline and 12 weeks.
Change in waist circumference (cm)
Change between baseline and 12 weeks.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

August 1, 2021

Primary Completion (Anticipated)

March 1, 2023

Study Completion (Anticipated)

January 1, 2025

Study Registration Dates

First Submitted

June 28, 2019

First Submitted That Met QC Criteria

July 2, 2019

First Posted (Actual)

July 5, 2019

Study Record Updates

Last Update Posted (Actual)

October 8, 2020

Last Update Submitted That Met QC Criteria

October 7, 2020

Last Verified

October 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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