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Clinical Trials/NCT00212290
NCT00212290CompletedPhase 4

Insulin Resistance and Central Nervous System (CNS) Function in Type 2 Diabetes

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)4 sites in 1 country140 target enrollmentStarted: November 2002Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
140
Locations
4
Primary Endpoint
Verbal memory (main study)

Study Overview

Brief Summary

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.

Detailed Description

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double

Eligibility Criteria

Ages
55 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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
  • 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

Outcomes

Primary 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

Investigators

Study Sites (4)

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