Overview

Rosiglitazone Effects on Cognition for Adults in Later Life

Status:
Unknown status
Trial end date:
2011-12-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to determine the effects of the insulin-sensitizing medication rosiglitazone on attention and memory skills in older adults with mild cognitive impairment (MCI). The study also will examine the effects of this medication on brain structures that support memory and other thinking abilities, and on biological markers associated with inflammation, insulin resistance, and cardiovascular disease.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Washington
Collaborators:
GlaxoSmithKline
National Institute on Aging (NIA)
Treatments:
Rosiglitazone
Criteria
Inclusion Criteria:

- MCI diagnosis: Participants will be diagnosed with MCI by consensus of a team of
physicians and neuropsychologists experienced in the diagnosis of MCI, using the
Petersen (Petersen, 1999, 2001) criteria for amnestic MCI or multiple domain MCI with
amnestic features: a) the presence of subjective memory complaints, evaluated via
detailed patient history and informant interview, b) objective verification of memory
impairment as measured by neuropsychological tests, c) normal general cognitive
function, d) intact or only mildly impaired activities of daily living, and e) absence
of dementia per NINCDS/ADRDA and/or DSM-IV criteria

Exclusion Criteria:

The following exclusion criteria will be used, based on initial physical examination,
medical history, lab work, and oral glucose tolerance test (OGTT) results:

- Diagnosis of diabetes or other relevant glucoregulatory disorders

- Use of any oral anti-diabetic compounds

- Clinically significant elevations in liver function

- Significant neurological disease that might affect cognition, other than MCI,
including Alzheimer's disease, large-vessel stroke, Parkinson's disease, multiple
sclerosis, recent severe head injury (loss of consciousness for more than 30 minutes
in the past year), or remote head injury resulting in permanent cognitive or
neurological sequelae

- History or current evidence of congestive heart failure (CHF)

- History of documented ischemic cardiac disease, i.e., angina, MI, angioplasty, stent,
or CABG

- History of cardiac or vascular surgery, or significant arrhythmia within the last
year; or planned major intervention such as cardiac surgery or stenting. A history of
cardiac surgery for non-ischemic indications (i.e., valve repair or replacement)
greater than one year prior to enrollment is not exclusionary if all other criteria
are met

- Significant ECG abnormalities including heart rate less than 50 or greater than 100
beats per minute (dependent upon the individual's general health); any previously
unrecognized arrhythmia requiring further intervention

- Significant peripheral edema at the time of screening

- Significant medical illness or organ failure, including but not limited to renal
disease, hepatic disease, and unstable cardiac disease

- Regular current use of antipsychotic, anticonvulsive, anxiolytic, or sedative
medications; antidepressant medications are not exclusionary, provided the individual
does not have current major depression

- A current diagnosis of major depression or other significant psychiatric comorbidity

- Clinically significant anemia at the time of screening

- Fasting triglyceride level greater than 400

- Fasting glucose 125 or greater, or two-hour glucose value greater than 199 during the
OGTT; participants will be notified if their fasting blood sugar (monitored every 3
months) exceeds 125, and they will be withdrawn from further participation if their
fasting blood sugar exceeds 125 for two consecutive months

- For the MRI substudy, additional exclusion criteria include 1) previous exposure to
work involving the cutting or grinding of metal, 2) the presence of a pacemaker,
aneurysm clip, or other implanted metal device that would prohibit MRI procedures, and
3) significant history of claustrophobia