Influence of Moderate Exercise on Blood Glucose in Type 2 Diabetics and Healthy Controls (DIEGO)

February 21, 2014 updated by: Merethe Hansen, University of Copenhagen

Influence of Moderate Exercise on Blood Glucose in Type 2 Diabetics and Healthy Controls.

Project description

Research project title:

Influence of moderate exercise on blood glucose in type 2 diabetics and healthy controls.

Project description and objective

Obesity is so widespread in Denmark that 47% of the population is classed as overweight (BMI>=25) and around 13% of the population is classed as obese (BMI>=30).

The strong correlation between obesity and type 2 diabetes (at least 2/3 of type 2 diabetics are overweight) has led to many studies which look at different forms of exercise for this group, because weight loss may improve the diabetes and even defer the onset of the disorder and in doing so lower complications and increase long term survival.

For people who do not have type 2 diabetes, the work-induced increased sympathetic activity will lead to suppressed insulin secretion and increased glucagon secretion. This increases the endogenous glucose production from the liver and thus maintains a normal concentration of blood sugar in a physical training situation where the demand for glucose has increased.

The theory behind the project is that the mechanisms that help to increase glucose production in the liver during physical activity are weaker in type 2 diabetics, which can cause hypoglycaemia during and after physical exercise. In other words, we want to study the liver's sensitivity to stimulus from physical work by patients with type 2 diabetes and in relevant healthy control subjects.

Previous studies have indicated that this type of mechanism is not intact in type 2 diabetics; because the level of insulin does not fall as expected during or after physical training. However, there are no existing studies that measure the liver's glucose secretion using stable isotopes during prolonged moderate physical work. Measuring this will help to clarify our understanding of glucose homeostasis in type 2 diabetics.

This study is very relevant, because it may be expected that the preferred form of physical exercise of an overweight type 2 diabetic can be of moderate intensity and previous studies also show that this form of physical exercise delivers health gains in terms of an improvement in insulin sensitivity and a reduction in the level of insulin.

The objective of this study is to determine if the level of blood glucose stays constant before, during and after physical training and to examine the liver's ability to secret glucose accordingly.

Study Overview

Detailed Description

Design

A group of 20 people with type 2 diabetes and 10 control subjects are twice invited to the laboratory, respectively.

The type 2 diabetes group consist of 10 individuals being treated with metformin and 10 individuals who are not being treated with Metformin. The latter group may be diet-treated diabetics or diabetics who have stopped taking their oral antidiabetic agent for 72 hours before the day of the experiment.

On the first visit, the following is carried out:

  • DXA scan, blood pressure measurement, determination of ECG and VO2-max on a cycleergometer
  • Blood sample
  • Questionnaire about everyday physical activity (I-PAQ)

On the second visit, the following is carried out:

  • 3 days of carbohydrate loading prior to this day.(By diet recommendations).
  • Insertion of arterial cannula, blood sample extraction.
  • Insertion of venus cannula. Insertion of stable glucose isotopes over a period of 4.5 hours: 2,5 hours of relaxation in bed followed by 45 minutes of cycling on an exercise bicycle (during continued isotope infusion) at 60% of maximum heart rate reserve, which was measured on test day 1. Followed by relaxation with continued blood sampling and isotope infusion, one hour after cycling ceased.

Inclusion criteria

  • Age between 30 and 60 years old,
  • Maximum oxygen consumption between 20 and 50 ml/kg/minute,
  • BMI between 25 and 35 kg/m2,
  • Normal ECG,
  • Must have a stable weight throughout the last three months and have a normal balanced diet,
  • Can cycle for 45 minutes

Exclusion criteria

  • For patients with type 2 diabetes: insulin treatment,
  • ECG that indicates cardiovascular disease,
  • Illness or medicine that may affect the results,
  • On-going weight loss diet

DXA scan

Minimal radiation - The scan lasts from six to 10 minutes and the total radiation dose with measuring is below 0.01 mSv (millisievert). This is approximately equivalent to the natural daily background exposure.

Cycling test

Prior to this test, an ECG is carried out and the person is quizzed about his/her state of health. Regarding all experiments, there is quick access to doctors in the laboratory. The laboratory is equipped with a defibrillator.

Infusion with stable glucose isotopes

Stable glucose isotopes occur naturally in the body, though in much smaller amounts. They are not radioactive and require no special precautions.

Blood sampling

An arterial cannula is inserted, from which blood samples are subsequently taken. A sample is immediately analysed (ABL analyser) for glucose and lactate concentrations and blood gases, Hgb and Hct.

Other blood samples are processed on a centrifuge and the plasma is frozen at - 80 °C until it will be analysed.

The plasma is analysed to determine concentrations of:

Insulin, glucagon, cortisol, growth hormone (GH), adrenocorticotrophic hormone (ACTH),C-peptide, catecholamines , alanin, concentration of ketone, cholesterol free fatty acids,glycerol, glucose isotope (Ra) content before, during and after the cycling.

The biological material (in the form of plasma) will be stored in a freezer. When the experiment is completed, the material will be analysed in our laboratories. When all of the analysis has been carried out, any excess materials will be destroyed. All materials will be stored anonymously.

Ethical considerations

At all times, the study will be carried out in accordance with the latest of Helsinki and current Danish legislation.

Among other things, this includes voluntary participation and that test subjects can withdraw their consent at any time and without having to provide any explanation.

The study protocol and the written patient information will be submitted to the Research Ethics Committee of the Capital Region of Denmark and the Danish Data Protection Agency will be informed. Patient inclusion cannot begin until a written approval has been received from both of these institutions. Both positive and, negative and inconclusive results must be published.

Study Type

Observational

Enrollment (Actual)

24

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

      • Copenhagen, Denmark, 2200
        • XLab, Center for Healthy Aging, Department of Biomedical Sciences, University of Copenhagen

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 60 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Sampling Method

Probability Sample

Study Population

  • 10 type 2 Diabetics without medication
  • 10 type 2 Diabetics on Metformin treatment
  • 10 matched healthy controls

Description

Inclusion Criteria:

  • Age between 30 and 60 years old
  • Maximum oxygen consumption between 20 and 50 ml/kg/minute
  • BMI between 25 and 35 kg/m2
  • Normal ECG
  • Must have a stable weight throughout the last three months and have a normal balanced diet
  • Can cycle for 45 minutes

Exclusion Criteria:

  • For patients with type 2 diabetes: insulin treatment
  • ECG that indicates cardiovascular disease
  • Illness or medicine that may affect the results
  • On-going weight loss diet

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Normal glucose tolerance subjects
Healthy controls. If any medication then paused 3 days prior to test days. BMI: 20-35. VO2max: 20-50. Age: 30-60 years All subjects perform same tests. - See protocol for description.
Other Names:
  • exercise performed at 60% of heart rate reserve.
DM2

Type 2 diabetics in diet treatment or type 2 diabetics who have paused their oral medication for 3 whole days.

Insulin treatment is an exclusion criteria. If any other medication then paused 3 days prior to test days.

BMI: 20-35. VO2max: 20-50. Age: 30-60 years All subjects perform same tests. - See protocol for description.

Other Names:
  • exercise performed at 60% of heart rate reserve.
DM2 + Metformin

Type 2 diabetics in metformin treatment. Insulin treatment is an exclusion criteria. If any other medication (besides from metformin) then paused 3 days prior to test days.

BMI: 20-35. VO2max: 20-50. Age: 30-60 years All subjects perform same tests. - See protocol for description

Other Names:
  • exercise performed at 60% of heart rate reserve.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Glucose homeostasis in controls, type 2 diabetics without medication and type 2 diabetics in metformin treatment.
Time Frame: Observational study. Glucose homeostasis is tested one day only (in our Lab). Samples are taken 2,5 hours before, during and untill 1 hour after 45 minutes of exercise. Samples are taken every 5 minutes.

Glucose, hormones, substrates, metabolites and glucose-isotopes as mentioned in the protocol.

These end points will be measured on test day 2 only. Hormones and metabolites will be measured as AUC and total concentrations.

Observational study. Glucose homeostasis is tested one day only (in our Lab). Samples are taken 2,5 hours before, during and untill 1 hour after 45 minutes of exercise. Samples are taken every 5 minutes.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
MAP during moderate exercise
Time Frame: 45 min of moderate exercise (test day 2).
MAP is continuously measured during exercise for 45 mins. (At 60% heart rate reserve)
45 min of moderate exercise (test day 2).
vo2max
Time Frame: one measurement each subject (test day 1)
Is measured in all subjects prior to test day 2
one measurement each subject (test day 1)
DXA-values
Time Frame: one measurement each subject (test day 1)
DXA (fat%, lean body mass, BMD)is measured prior to test day 2
one measurement each subject (test day 1)
IL-6 and incretins
Time Frame: Observational study. Each test subject is tested for IL-6 and incretins one day only (in our Lab), where blood samples are taken continously during the test day every 5 minutes before, during and after exercise (test day 2).
Effect of exercise on IL-6 and incretins. Described as AUC and total concentrations.
Observational study. Each test subject is tested for IL-6 and incretins one day only (in our Lab), where blood samples are taken continously during the test day every 5 minutes before, during and after exercise (test day 2).

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Flemming Dela, professor, University of Copenhagen

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

October 1, 2012

Primary Completion (Actual)

November 1, 2013

Study Completion (Actual)

November 1, 2013

Study Registration Dates

First Submitted

November 30, 2012

First Submitted That Met QC Criteria

January 8, 2013

First Posted (Estimate)

January 10, 2013

Study Record Updates

Last Update Posted (Estimate)

February 24, 2014

Last Update Submitted That Met QC Criteria

February 21, 2014

Last Verified

February 1, 2014

More Information

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.

Clinical Trials on Type 2 Diabetes and Exercise

Clinical Trials on 45 minutes of moderate exercise at the fasted state. Before test day 2: 3 days of carbohydrate loading.

3
Subscribe