Lipitor as a Treatment for Alzheimer's Disease
Information source: National Institute on Aging (NIA)
Information obtained from ClinicalTrials.gov on March 21, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Alzheimer Disease
Intervention: Atorvastatin calcium (Drug)
Phase: Phase 2
Status: Completed
Sponsored by: Institute for the Study of Aging (ISOA) Official(s) and/or principal investigator(s): David L Sparks, PhD, Principal Investigator, Affiliation: Sun Health Research Institute
Summary
The purpose of this study is to assess the clinical benefit of Lipitor, a
cholesterol-lowering drug, in the treatment of Alzheimer's disease.
Clinical Details
Official title: Effect of the HMG-CoA Reductase Inhibitor Atorvastatin Calcium, Lipitor, in the Treatment of Alzheimer's Disease
Study design: Treatment, Randomized, Double-Blind, Placebo Control, Efficacy Study
Detailed description:
This study is a phase II, placebo controlled, double-blind, one year trial investigating the
effect of HmG-CoA reductase inhibitor atorvastatin calcium in the treatment of persons with
possible or probable Alzheimer's disease. Subjects may continue to take stable doses of
Aricept and Exelon. Following enrollment, participants will make visits to the study center
every three months for blood tests and neuropsychological testing.
Eligibility
Minimum age: 50 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Prior to participation in this study, each prospective study individual must sign an
informed consent form.
- Diagnosis of probable or possible Alzheimer's disease according to NINDS-ADRDA and
DSM-IV criteria.
- Not actively participating in another clinical drug trial.
- MMSE range 12-28 at entry.
- Hachinski Modified Ischemic score < or =4.
- Accompanied by appropriate caregiver who can aid in administration of medication and
make assessments.
- Good general health as evidenced by physical, neurological and clinical laboratory
examination.
- Education level > or = 9th grade or equivalent.
- Fluent in the English language.
- Reliable caregiver.
- Able to complete neuropsychological tests.
- Ambulatory.
- On stable doses of medications for the treatment of non-excluded medical conditions
for four weeks prior to screening.
- Able to participate in all scheduled evaluations.
- Geriatric Depression Scale < or = 20.
- Not exceeding 400 IU of Vitamin E for 30 days.
- For patients currently taking donepezil, they must remain on a stable dose for at
least three months. Individuals taking stable doses of other cholinesterase
inhibitors can be included, but no study subject may initiate use of any
cholinesterase inhibitor after entrance to trial.
- Individuals of both sexes over 50 years of age will be eligible.
Exclusion criteria:
- Significant neurological or psychiatric disease other than Alzheimer's disease.
- Patients with known or suspected Parkinsons's disease or dementia with Lewy bodies.
- Significant systemic illness (including uncontrolled hypertension) or organ failure.
- History of mental illness within one year or history of significant untreated cardiac
or thromboembolic vascular disease (arrythmias, unstable angina, CVA, deep venous
thrombosis, or pulmonary embolus).
- Current chronic use of anti-cholinergic medications (anti-histamines, and Artane or
Cogentin). Stable doses of anxiolytics, sedatives, hypnotics, antipsychotics and SSRI
antidepressants are acceptable. The use of any antipsychotics or tricyclic
anti-depressants must be reviewed prior to entry.
- Diagnosis of major depression according to DSM-IV criteria in the last two years.
- Allergies to atorvastatin or HMG CoA reductase inhibitors.
- Pregnant women.
- History of head injury.
- On a cholesterol lowering drug at time of enrollment.
- History of significant liver disease and or elevated transaminases.
- Cholesterol level lower than 90 mg% at initial screening
Locations and Contacts
Sun Health Research Institute, Sun City, Arizona 85351, United States
Additional Information
Sun Health Research Institute
Related publications: Sparks DL. Intraneuronal beta-amyloid immunoreactivity in the CNS. Neurobiol Aging. 1996 Mar-Apr;17(2):291-9. Sparks DL. Coronary artery disease, hypertension, ApoE, and cholesterol: a link to Alzheimer's disease? Ann N Y Acad Sci. 1997 Sep 26;826:128-46. Sparks DL, Martin TA, Gross DR, Hunsaker JC 3rd. Link between heart disease, cholesterol, and Alzheimer's disease: a review. Microsc Res Tech. 2000 Aug 15;50(4):287-90. Review. Sparks DL, Lopez J, Connor D, Sabbagh M, Seward J, Browne P; Alzheimer's Disease Cholesterol-Lowering Treatment Team. A position paper: based on observational data indicating an increased rate of altered blood chemistry requiring withdrawal from the Alzheimer's Disease Cholesterol-Lowering Treatment Trial (ADCLT). J Mol Neurosci. 2003;20(3):407-10. Sparks DL, Connor DJ, Browne P, Sabbagh MN; AD Cholesterol-Lowering Treatment Trial Team. Should the guidelines for monitoring serum cholesterol levels in the elderly be re-evaluated? J Mol Neurosci. 2002 Aug-Oct;19(1-2):209-12.
Starting date: October 2000
Ending date: August 2004
Last updated: November 8, 2006
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