HDL Proteomics: Plaque Inflammation and Dysfunctional HDL in AIM-HIGH

Sponsor
University of Washington (Other)
Overall Status
Completed
CT.gov ID
NCT00880178
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
324
29
40
11.2
0.3

Study Details

Study Description

Brief Summary

Coronary heart disease (CHD) is a serious health concern that affects millions of people in the United States. It is usually caused by atherosclerosis-a condition that occurs when fatty material and plaque build up on the walls of the arteries that supply blood and oxygen to the heart, causing the arteries to narrow. As the arteries narrow, blood flow to the heart can slow down or stop, which can cause chest pain, shortness of breath, heart attack, or heart failure. Another component of CHD events involves inflammatory changes that result in structural breakdown of atherosclerotic plaques. Adding niacin to statin medications may be an effective way to block inflammation in the atherosclerotic plaques. This study will examine magnetic resonance imaging (MRI) images and blood samples of participants in the AIM-HIGH study who are taking niacin plus statins or statins alone to determine the effect of these medications on inflammation in atherosclerotic plaques.

Condition or Disease Intervention/Treatment Phase

Detailed Description

CHD is the leading cause of death in the United States. Preliminary research has shown that CHD is associated with oxidative and inflammatory changes in high-density lipoprotein (HDL) cholesterol, which is considered the "good" cholesterol. The inflammatory changes can impair HDL cholesterol's normal function, which is to remove excess cholesterol from the arteries and thereby slow the build-up of atherosclerotic plaque. Statins are cholesterol-lowering medications that are used to treat people with CHD. Taking niacin, a type of B vitamin, in combination with statins may stabilize atherosclerotic plaques better than statins alone, but more research is needed to examine how niacin may do this. By improving the ability of HDL cholesterol to repair inflammatory damage to atherosclerotic plaques, niacin may assist in preventing the inflammation that leads to plaque breakdown.

The AIM-HIGH study (NCT00120289) is examining the use of niacin plus statins in people with vascular disease. Participants in the AIM-HIGH study are randomly assigned to receive either niacin plus simvastatin, which is a type of statin medication, or simvastatin alone. The purpose of this substudy is to determine whether niacin in combination with statins reduces atherosclerotic plaque inflammation and dysfunctional HDL cholesterol more than statins alone. The substudy will enroll participants who are participating in the AIM-HIGH study. At the AIM-HIGH baseline and Year 2 study visits, study researchers for this substudy will collect an additional blood sample from participants to examine the changes in HDL oxidation levels and protein composition at both time points. Study researchers will also analyze participants' MRI scans to examine changes in plaque inflammation during the study period; these MRI scans will be completed as part of another AIM-HIGH substudy, conducted by Dr. Xue-Qiao Zhao. There will be no additional study procedures or visits for participants in this substudy.

Study Design

Study Type:
Observational
Actual Enrollment :
324 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Plaque Inflammation and Dysfunctional HDL in AIM-HIGH
Study Start Date :
May 1, 2008
Actual Primary Completion Date :
Aug 1, 2011
Actual Study Completion Date :
Sep 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Simvastatin

Participants in the main AIM-HIGH study who are receiving simvastatin.

Drug: Simvastatin
Participants will be enrolled in this substudy only if they are candidates for the main AIM-HIGH study (NCT00120289). Participants will be randomly assigned to simvastatin or simvastatin plus niacin as a part of the main AIM-HIGH protocol, and adjustments in simvastatin and/or niacin doses will be made as per the protocol for the main AIM-HIGH study.

Simvastatin and Extended-Release Niacin

Participants in the main AIM-HIGH study who are receiving simvastatin and extended-release niacin.

Drug: Simvastatin and Extended-Release niacin
Participants will be enrolled in this substudy only if they are candidates for the main AIM-HIGH study (NCT00120289). Participants will be randomly assigned to simvastatin or simvastatin plus niacin as a part of the main AIM-HIGH protocol, and adjustments in simvastatin and/or niacin doses will be made as per the protocol for the main AIM-HIGH study.
Other Names:
  • Simvastatin/Niacin
  • Outcome Measures

    Primary Outcome Measures

    1. Change in HDL oxidation and proteomics [Measured at Year 2]

    Secondary Outcome Measures

    1. Comparison of HDL oxidation and proteomics changes between participants receiving statins versus participants receiving statins plus niacin [Measured at Year 2]

    2. Comparison of change in an MRI marker of plaque inflammation between participants receiving statins versus participants receiving statins plus niacin [Measured at Year 2]

    3. Comparison of changes in HDL oxidation and proteomics with change in an MRI marker of plaque inflammation [Measured at Year 2]

    4. Change in an MRI marker of plaque inflammation [Measured at Year 2]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Eligible for main AIM-HIGH study (NCT00120289)

    • Willing to provide informed consent for participation in this substudy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Cardiovascular Associates Birmingham Alabama United States 35213
    2 Cardiovascular Consultants Phoenix Arizona United States 85032
    3 Long Beach VA Medical Center Long Beach California United States 90822
    4 Christiana Care Health Services Newark Delaware United States 19718
    5 University of Maryland Baltimore Maryland United States 21201
    6 University of Minnesota Minneapolis Minnesota United States 55414
    7 HealthPartners Riverside Clinic Minneapolis Minnesota United States 55454
    8 Mayo Clinic Rochester Minnesota United States 55905
    9 Duke University Durham North Carolina United States 27710
    10 Wake Forest University, Geriatrics Greensboro North Carolina United States 27157
    11 Wake Forest University, Cardiology Winston-Salem North Carolina United States 27157
    12 Wake Forest University, Endocrinology Winston-Salem North Carolina United States 27157
    13 St. Vincent Charity Hospital Cleveland Ohio United States 44115
    14 Portland VA Medical Center Portland Oregon United States 97239
    15 Philadelphia VA Medical Center Philadelphia Pennsylvania United States 19104
    16 Pennsylvania Cardiology Associates Philadelphia Pennsylvania United States 19106
    17 Cardiology Consultants of Philadelphia Philadelphia Pennsylvania United States 19148
    18 Baylor College of Medicine Houston Texas United States 77030
    19 Kelsey Research Foundation Houston Texas United States 77030
    20 Methodist Hospital Houston Texas United States 77030
    21 McGuire VA Medical Center Richmond Virginia United States 23249
    22 Harborview Medical Center Seattle Washington United States 98104
    23 University of Washington Seattle Washington United States 98105
    24 Puget Sound VA Medical Center, Seattle Campus Seattle Washington United States 98108
    25 Heart Health Institute Calgary Alberta Canada T2E-7C5
    26 University of Calgary Calgary Alberta Canada T2N-2T9
    27 Vancouver General Hospital Vancouver British Columbia Canada V5Z-1M9
    28 University of Western Ontario London Ontario Canada N6A-5A5
    29 St. Michael's Health Centre Toronto Ontario Canada M5C-2T2

    Sponsors and Collaborators

    • University of Washington
    • National Heart, Lung, and Blood Institute (NHLBI)

    Investigators

    • Principal Investigator: Kevin D. O'Brien, MD, University of Washington

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Kevin O'Brien, Professor of Medicine, Cardiology, University of Washington
    ClinicalTrials.gov Identifier:
    NCT00880178
    Other Study ID Numbers:
    • 28201
    • R01HL089504
    First Posted:
    Apr 13, 2009
    Last Update Posted:
    May 14, 2018
    Last Verified:
    Feb 1, 2018

    Study Results

    No Results Posted as of May 14, 2018