Skip to content

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

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00212290
Enrollment
140
Registered
2005-09-21
Start date
2002-11-30
Completion date
2006-12-31
Last updated
2010-02-15

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

Conditions

Insulin Resistance, Type 2 Diabetes Mellitus

Keywords

impaired glucose tolerance

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.

Interventions

DRUGpioglitazone
DRUGplacebo

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
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 * 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

Design outcomes

Primary

MeasureTime frame
Beta-amyloid in spinal fluid (sub-study)
Plasma beta-amyloid levels (main study)
Cerebral glucose metabolism (sub-study)
Inflammatory markers in spinal fluid (sub-study)
Verbal memory (main study)
Selective attention (main study)

Secondary

MeasureTime frame
Verbal fluency
Blood levels of insulin, insulin degrading enzyme, cortisol and inflammatory markers
Psychomotor speed

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026