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Evaluating Simvastatin's Potential Role in Therapy (ESPRIT)

Primary Purpose

Alzheimer Disease

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Simvastatin
Placebo
Sponsored by
University of Wisconsin, Madison
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Alzheimer Disease focused on measuring amyloid protein, apolipoprotein, cerebrospinal fluid, cerebrovascular circulation, inflammation, magnetic resonance imaging, prevention & control

Eligibility Criteria

35 Years - 69 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age 35 to 69
  • Parent with Alzheimer's disease

Exclusion Criteria:

  • Current use of cholesterol-lowering medication
  • Active liver disease
  • History of adverse reaction to statins
  • Contraindication to lumbar puncture
  • Elevated lab values (creatine kinase and creatinine)
  • Use of medications known to interact with statins
  • History of dementia
  • Currently pregnant or planning to become pregnant
  • Use of large quantities of grapefruit juice (more than 1 quart per day)
  • Current involvement in another investigational drug study
  • Contraindications to MRI (for MRI sub-study)
  • Ethical contraindication to placebo (persons with high vascular risk)

Sites / Locations

  • University of Wisconsin

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

simvastatin

Placebo

Arm Description

simvastatin 40 mg nightly for 1 month then 80 mg nightly for 8 months

Matching placebo tablet nightly for 9 months

Outcomes

Primary Outcome Measures

Change in Cerebrospinal Fluid (CSF) Beta-amyloid-42

Secondary Outcome Measures

Changes in Regional Cerebral Blood Flow on MRI
Mean changes noted in posterior cingulate cortex
Change in Inflammatory Markers
Change noted in serum high-sensitivity c-reactive protein
Changes in Cognitive Performance
Change in Hopkins Verbal Learning Test Delayed Recall The Hopkins Verbal Learning Test Delayed Recall score is the raw number of words recalled at Trial 4, adjusted for years of education and age. This is a 12-item word list test.

Full Information

First Posted
June 12, 2007
Last Updated
February 14, 2019
Sponsor
University of Wisconsin, Madison
Collaborators
National Institute on Aging (NIA), Paul Beeson Faculty Scholars Program, The John A. Hartford Foundation, The Atlantic Philanthropies, Starr Foundation, American Federation for Aging Research, Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT00486044
Brief Title
Evaluating Simvastatin's Potential Role in Therapy
Acronym
ESPRIT
Official Title
Effect of Statins on Pathobiology of Alzheimer's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
February 2005 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
June 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Wisconsin, Madison
Collaborators
National Institute on Aging (NIA), Paul Beeson Faculty Scholars Program, The John A. Hartford Foundation, The Atlantic Philanthropies, Starr Foundation, American Federation for Aging Research, Merck Sharp & Dohme LLC

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to see how simvastatin, a cholesterol-lowering drug, affects processes related to the development of Alzheimer's disease, including: 1) levels of a substance called beta-amyloid-42 found in the spinal fluid surrounding the brain, 2) blood flow in the brain, 3) inflammation in the brain, and 4) cognitive function.
Detailed Description
Some studies suggest that statin medications, which are a group of cholesterol-lowering medicines, may help prevent Alzheimer's disease. However, this has not been proven in humans. The purpose of this study is to see how simvastatin affects a substance in the spinal fluid around the brain called beta-amyloid-42 which is thought to contribute to Alzheimer's disease. This study also evaluates whether simvastatin improves regional brain blood flow (on magnetic resonance imaging [MRI]), reduces inflammation, and improves cognitive function. The ESPRIT study was a 9-month randomized, controlled clinical trial that randomized 100 middle-aged adults with a parental history of Alzheimer's disease. Participants were randomized to simvastatin 40 mg for one month then 80 mg daily or matching placebo tablets. Fifty of the ESPRIT subjects participated in the MRI sub-study. Participants had the following data collected: fasting blood tests (baseline and months 3 and 9), medical history and medication questionnaires (each visit), study medication side effect review (all visits), lumbar puncture procedure (baseline and month 9), memory testing (baseline and months 3 and 9), and MRI (baseline and month 9 in 50 sub-study participants).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease
Keywords
amyloid protein, apolipoprotein, cerebrospinal fluid, cerebrovascular circulation, inflammation, magnetic resonance imaging, prevention & control

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
103 (Actual)

8. Arms, Groups, and Interventions

Arm Title
simvastatin
Arm Type
Experimental
Arm Description
simvastatin 40 mg nightly for 1 month then 80 mg nightly for 8 months
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Matching placebo tablet nightly for 9 months
Intervention Type
Drug
Intervention Name(s)
Simvastatin
Other Intervention Name(s)
Zocor
Intervention Description
40 mg tablet each night for one month, then 80 mg for 8 months
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Matching tablet each night for 9 months
Primary Outcome Measure Information:
Title
Change in Cerebrospinal Fluid (CSF) Beta-amyloid-42
Time Frame
baseline and 9 months
Secondary Outcome Measure Information:
Title
Changes in Regional Cerebral Blood Flow on MRI
Description
Mean changes noted in posterior cingulate cortex
Time Frame
baseline and 9 months
Title
Change in Inflammatory Markers
Description
Change noted in serum high-sensitivity c-reactive protein
Time Frame
baseline and 9 months
Title
Changes in Cognitive Performance
Description
Change in Hopkins Verbal Learning Test Delayed Recall The Hopkins Verbal Learning Test Delayed Recall score is the raw number of words recalled at Trial 4, adjusted for years of education and age. This is a 12-item word list test.
Time Frame
Baseline and 9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 35 to 69 Parent with Alzheimer's disease Exclusion Criteria: Current use of cholesterol-lowering medication Active liver disease History of adverse reaction to statins Contraindication to lumbar puncture Elevated lab values (creatine kinase and creatinine) Use of medications known to interact with statins History of dementia Currently pregnant or planning to become pregnant Use of large quantities of grapefruit juice (more than 1 quart per day) Current involvement in another investigational drug study Contraindications to MRI (for MRI sub-study) Ethical contraindication to placebo (persons with high vascular risk)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cynthia M. Carlsson, MD, MS
Organizational Affiliation
University of Wisconsin, Madison
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Wisconsin
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53705
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11296263
Citation
Fassbender K, Simons M, Bergmann C, Stroick M, Lutjohann D, Keller P, Runz H, Kuhl S, Bertsch T, von Bergmann K, Hennerici M, Beyreuther K, Hartmann T. Simvastatin strongly reduces levels of Alzheimer's disease beta -amyloid peptides Abeta 42 and Abeta 40 in vitro and in vivo. Proc Natl Acad Sci U S A. 2001 May 8;98(10):5856-61. doi: 10.1073/pnas.081620098. Epub 2001 Apr 10.
Results Reference
background
PubMed Identifier
11344276
Citation
Wolozin B. A fluid connection: cholesterol and Abeta. Proc Natl Acad Sci U S A. 2001 May 8;98(10):5371-3. doi: 10.1073/pnas.101123198. No abstract available.
Results Reference
background
PubMed Identifier
15734937
Citation
Johnson NA, Jahng GH, Weiner MW, Miller BL, Chui HC, Jagust WJ, Gorno-Tempini ML, Schuff N. Pattern of cerebral hypoperfusion in Alzheimer disease and mild cognitive impairment measured with arterial spin-labeling MR imaging: initial experience. Radiology. 2005 Mar;234(3):851-9. doi: 10.1148/radiol.2343040197.
Results Reference
background
Links:
URL
http://adrc.wisc.edu/
Description
Wisconsin Alzheimer's Disease Research Center

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Evaluating Simvastatin's Potential Role in Therapy

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