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Is Insulin Resistance and/or Glucose Intolerance Pathogenetic in the Development of a Reduced Incretin Effect

Is Insulin Resistance and/or Glucose Intolerance Pathogenetic in the Development of a Reduced Incretin Effect

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00784745
Enrollment
21
Registered
2008-11-04
Start date
2008-11-30
Completion date
2009-09-30
Last updated
2014-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glucose Intolerance, Insulin Resistance

Keywords

incretin effect, type 2 diabetes, GLP-1, GIP, dexamethasone

Brief summary

The purpose of this study is to examine whether there is a causal relationship between insulin resistance and/or glucose intolerance in the development of a defect incretin effect.

Detailed description

In this study we are going to examine the incretin effect before and after the development of insulin resistance and/or glucose intolerance. The incretin effect is the increased insulin response seen after an oral as apposed to an intravenous glucose challenge with identical plasma glucose profiles. This insulin enhancing effect is greatly reduced in type 2 diabetes. Since the development of type 2 diabetes is preceded by insulin resistance and glucose intolerance we wanted to examine the incretin effect in the early stages of type 2 diabetes. To do this, we want to induce insulin resistance and/or glucose intolerance. This is achieved by 5 days of treatment with dexamethasone. The incretin effect in this study will be examined by 3 investigations prior to the treatment and 3 days following the treatment. Day 1: Oral glucose challenge with 75 g of glucose. The subject is asked to drink 75g of glucose suspended in 300mL of water. During the 4 hours of the test, we draw blood at various times during the study to determine the concentration of: Glucose, GLP-1, GIP, Glucagon, Insulin and c-peptide. Day 2: Intravenous glucose We duplicate the glucose curve obtained from day 1. We also draw blood during this test to the same end as in day 1. Day 3: Mixed meal. The subjects are served a mixed meal. During this 4 hour test, we draw blood to examine the response to a standardized meal. The test involves sampling blood as described for the other days.

Interventions

DRUGDexamethasone

2mg morning and night for 5 days.

Sponsors

University Hospital, Gentofte, Copenhagen
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Caucasians \>20 years * Normal glucose tolerance as assessed by the WHO criteria * First degree relative and at least 1 second degree relative with type 2 diabetes * Normal haemoglobin * Informed consent

Exclusion criteria

* Liver disease (ALAT/ASAT \> 2 times normal value) * Kidney disease (S-creatinin \> 130uM and/or albuminuria) * Heart disease (NYHA II, III or IV) * Treatment with medicine that cannot be paused * Pregnancy of breast feeding

Design outcomes

Primary

MeasureTime frame
Incremental GLP-1 response during the mixed meal test. Assessed as AUC during the 4 hour test.4 hours (during the mixed meal test)

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026