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Effects of Atorvastatin on Disease Activity and HDL Cholesterol Function in Patients With Rheumatoid Arthritis

Primary Purpose

Rheumatoid Arthritis

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Atorvastatin
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rheumatoid Arthritis focused on measuring Rheumatoid arthritis, Atherosclerosis, High density lipoprotein (HDL) cholesterol, Statins, HDL anti-inflammatory properties, Atorvastatin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Fulfill American College of Rheumatology (ACR) criteria for RA At least 18 years of age Have RA for at least one year with ongoing active disease (active disease defined as at least two of three: 1) ≥ six tender joints; 2) ≥ three swollen joints; 3) ≥ 45 minutes of morning stiffness) Taking stable doses of disease modifying anti-rheumatic drug (DMARD) therapy for at least 3 months prior to study entry - Exclusion Criteria: Unable to give informed consent Pregnant or lactating Eligible for pharmacologic lipid-lowering therapy per National Cholesterol Treatment Program Adult Treatment Panel III guidelines Using any lipid lowering medication Known hepatic disease Elevated liver transaminase levels within the past two months Previous treatment in the last three months with hydroxychloroquine -

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Experimental

    Arm Label

    Placebo

    Atorvastatin

    Arm Description

    Placebo

    Atorvastatin

    Outcomes

    Primary Outcome Measures

    HDL anti-inflammatory properties at 0 and 12 weeks
    Highly sensitive C-reactive protein (hs-CRP) at 0 and 12 weeks

    Secondary Outcome Measures

    Disease activity score using a 28 joint count (DAS28) at 0,3,6,12, and 18 weeks
    Patient and physician global assessments on visual analogue pain scale (VAS; 0-100) at 0,3,6,12, and 18 weeks
    Swollen and tender joint counts at 0,3,6,12,and 18 weeks
    Patient pain assessment on VAS (0-100)at 0,3,6,12, and 18 weeks
    Erythrocyte sedimentation rate(Westergren) at 0,3,6,12, and 18 weeks
    Cholesterol levels at 0,3,6,12, and 18 weeks
    Health assessment questionnaire disability index (HAQ-DI) at 0,3,6,12, and 18 weeks

    Full Information

    First Posted
    July 25, 2006
    Last Updated
    June 21, 2012
    Sponsor
    University of California, Los Angeles
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00356473
    Brief Title
    Effects of Atorvastatin on Disease Activity and HDL Cholesterol Function in Patients With Rheumatoid Arthritis
    Official Title
    Effects of Atorvastatin on Disease Activity and HDL Cholesterol Anti-inflammatory Properties in Patients With Rheumatoid Arthritis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2006
    Overall Recruitment Status
    Completed
    Study Start Date
    March 2003 (undefined)
    Primary Completion Date
    September 2005 (Actual)
    Study Completion Date
    September 2005 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    University of California, Los Angeles

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This research evaluates the effects of a cholesterol-lowering medication, atorvastatin, on both arthritis activity and the ability of high-density lipoprotein cholesterol (HDL-C, sometimes referred to as "good cholesterol") to prevent changes in low-density lipoprotein cholesterol (LDL-C, sometimes referred to as "bad cholesterol"), which lead to atherosclerosis, or "hardening of the arteries." We hypothesize that atorvastatin may improve both joint inflammation and the anti-inflammatory properties of HDL cholesterol.
    Detailed Description
    Heart attacks are the leading cause of death in patients with rheumatoid arthritis (RA). Cardiovascular events occur more frequently than would be expected in patients with RA and traditional heart risk factors do not explain this increased risk. Further research is needed to pursue ways of reducing heart disease mortality and improving outcome in patients with RA. There is reason to believe that a class of cholesterol-lowering medications called statins, beneficial in cardiovascular disease prevention, may be able to reduce the irritation of the joints ("inflammation") associated with RA. Statins have been shown to reduce manifestations of inflammation in the blood of patients at increased risk for heart disease, and in the process reduce the risk of heart attack, stroke, and sudden death. Some similarities in the nature of both RA and heart disease may suggest potential benefits of statin therapy in both conditions. In addition to inflammation, another factor which may contribute to coronary heart disease (CHD) risk in RA patients is dysfunctional high-density lipoprotein cholesterol (HDL-C, sometimes referred to as "good cholesterol"). Normally, HDL-C acts to counter a type of damage called "oxidation" within LDL-C which is a critical step in the development and progression of heart disease. Data from patients with RA and system lupus erythematosus (SLE) suggests that patients with active rheumatic diseases such as RA and SLE may have increased amounts of dysfunctional HDL-C, and therefore they may be at increased risk of heart disease. A blood test developed by Dr. Navab and colleagues at UCLA rapidly assesses this HDL-C function. This study will investigate both the level of HDL-C antioxidant function in patients with active RA as well as whether abnormal HDL function can be improved by statin use in this population. This research also evaluates the effects of atorvastatin on arthritis activity. We hypothesize that atorvastatin may improve both joint inflammation and the anti-inflammatory properties of HDL cholesterol.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Rheumatoid Arthritis
    Keywords
    Rheumatoid arthritis, Atherosclerosis, High density lipoprotein (HDL) cholesterol, Statins, HDL anti-inflammatory properties, Atorvastatin

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    20 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo
    Arm Title
    Atorvastatin
    Arm Type
    Experimental
    Arm Description
    Atorvastatin
    Intervention Type
    Drug
    Intervention Name(s)
    Atorvastatin
    Primary Outcome Measure Information:
    Title
    HDL anti-inflammatory properties at 0 and 12 weeks
    Time Frame
    at 0 and 12 weeks
    Title
    Highly sensitive C-reactive protein (hs-CRP) at 0 and 12 weeks
    Time Frame
    at 0 and 12 weeks
    Secondary Outcome Measure Information:
    Title
    Disease activity score using a 28 joint count (DAS28) at 0,3,6,12, and 18 weeks
    Time Frame
    at 0,3,6,12, and 18 weeks
    Title
    Patient and physician global assessments on visual analogue pain scale (VAS; 0-100) at 0,3,6,12, and 18 weeks
    Time Frame
    at 0,3,6,12, and 18 weeks
    Title
    Swollen and tender joint counts at 0,3,6,12,and 18 weeks
    Time Frame
    at 0,3,6,12, and 18 weeks
    Title
    Patient pain assessment on VAS (0-100)at 0,3,6,12, and 18 weeks
    Time Frame
    at 0,3,6,12, and 18 weeks
    Title
    Erythrocyte sedimentation rate(Westergren) at 0,3,6,12, and 18 weeks
    Time Frame
    at 0,3,6,12, and 18 weeks
    Title
    Cholesterol levels at 0,3,6,12, and 18 weeks
    Time Frame
    at 0,3,6,12, and 18 weeks
    Title
    Health assessment questionnaire disability index (HAQ-DI) at 0,3,6,12, and 18 weeks
    Time Frame
    at 0,3,6,12, and 18 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Fulfill American College of Rheumatology (ACR) criteria for RA At least 18 years of age Have RA for at least one year with ongoing active disease (active disease defined as at least two of three: 1) ≥ six tender joints; 2) ≥ three swollen joints; 3) ≥ 45 minutes of morning stiffness) Taking stable doses of disease modifying anti-rheumatic drug (DMARD) therapy for at least 3 months prior to study entry - Exclusion Criteria: Unable to give informed consent Pregnant or lactating Eligible for pharmacologic lipid-lowering therapy per National Cholesterol Treatment Program Adult Treatment Panel III guidelines Using any lipid lowering medication Known hepatic disease Elevated liver transaminase levels within the past two months Previous treatment in the last three months with hydroxychloroquine -
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Benjamin J Ansell, MD
    Organizational Affiliation
    University of California, Los Angeles
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    17552046
    Citation
    Charles-Schoeman C, Khanna D, Furst DE, McMahon M, Reddy ST, Fogelman AM, Paulus HE, Park GS, Gong T, Ansell BJ. Effects of high-dose atorvastatin on antiinflammatory properties of high density lipoprotein in patients with rheumatoid arthritis: a pilot study. J Rheumatol. 2007 Jul;34(7):1459-64. Epub 2007 Jun 1.
    Results Reference
    derived

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    Effects of Atorvastatin on Disease Activity and HDL Cholesterol Function in Patients With Rheumatoid Arthritis

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