NCT Number: NCT00212290
Insulin Resistance and Central Nervous System (CNS) Function in Type 2 Diabetes
The purpose of this study is to examine the effects of treating insulin resistance on memory and attention, brain glucose utilization, and proteins in spinal fluid.
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Conditions
Age range
55 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
VA Puget Sound Health Care System (Seattle Campus), Seattle, Washington, United States
About this study
Insulin resistant conditions such as impaired glucose tolerance, type 2 diabetes mellitus, and hyperinsulinemia have been associated with an increased risk for memory decline and for Alzheimer's disease. The main study will determine whether treatment with pioglitazone or nateglinide will improve verbal memory and selective attention for older adults with impaired glucose tolerance or mild type 2 diabetes. The main study will also characterize changes in blood concentrations of insulin, inflammatory markers, and the beta-amyloid peptides that are related to Alzheimer's disease. In one sub-study, participants will undergo brain positron emission tomography (PET) imaging before and after 16 weeks of treatment with pioglitazone, nateglinide, or placebo. The purpose of this sub-study is to determine the effects of treatment on brain glucose utilization. In a second sub-study, participants will undergo a lumbar puncture procedure before and after treatment. The purpose of this sub-study is to determine the effects of treatment on spinal fluid concentrations of insulin, inflammatory markers, and beta-amyloid peptides. Together these main and sub-studies should characterize the effects of insulin resistance on cognition and suggest a mechanism by which insulin resistant conditions increase risk for memory decline and for Alzheimer's disease.
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Impaired glucose tolerance OR mild type 2 diabetes mellitus OR normal blood sugar regulation
- Stable weight and activity level
Exclusion criteria
- Medications for diabetes
- Dementia
- Medications with known effects on memory
- Serious neurologic disease or head trauma
- Serious systemic illness (e.g., renal failure or uncontrolled hypertension)
- Serious psychiatric illness (e.g., schizophrenia or bipolar disorder)
- Allergy to pioglitazone or nateglinide
Treatment and study plan
nateglinide
DrugPlacebo
DrugPrimary outcomes
-
Verbal memory (main study)
-
Selective attention (main study)
-
Plasma beta-amyloid levels (main study)
-
Cerebral glucose metabolism (sub-study)
-
Inflammatory markers in spinal fluid (sub-study)
-
Beta-amyloid in spinal fluid (sub-study)
Secondary outcomes
-
Psychomotor speed
-
Verbal fluency
-
Blood levels of insulin, insulin degrading enzyme, cortisol and inflammatory markers
Sponsors and collaborators
Lead sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Nih
Registry information
Important dates
- Study start
- 2002
- Study completion
- 2006
- First posted
- Sep 21, 2005
- Registry last updated
- Feb 15, 2010
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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