search
Back to results

Statins and Lupus: Effects of Statins on Clinical Lupus Parameters, Serological Markers and Toll-like Receptors

Primary Purpose

Systemic Lupus Erythematosus

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
atorvastatin
Sponsored by
The Center for Rheumatic Disease, Allergy, & Immunology
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Systemic Lupus Erythematosus focused on measuring Lupus, TLR's, Hyperlipidemia, age eighteen to sixty, female with SLE, SLEDAI, greater than four, LDL cholesterol elevated

Eligibility Criteria

18 Years - 60 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-60, female
  • have at least four ACR criteria for SLE
  • SLEDAI score > 4
  • LDL cholesterol level from 100-190mg/dl

Exclusion Criteria:

  • Pregnant, lactating, or wanting to become pregnant
  • unable to take atorvastatin due to allergy, liver disease, elevated lever function test, myositis, or eleveated CPK
  • already on lipid lowering therapy
  • participating in another lupus study
  • on drugs such as: amiodarone, clarithromycin, clclosporine, erythromycin, itraconazole, ketoconazole, nefazodone, verapamil, protease inhibitors, niacin, digoxin, cholestryrmine, colestipol
  • has a diagnosis of myositis

Sites / Locations

  • The Center for Rheumatic Disease, Allergy, and Immunology

Outcomes

Primary Outcome Measures

decrease the SLEDAI level of female lupus patients, down regulate the TLR 2,4, and 9.

Secondary Outcome Measures

lower lipid levels in female lupus patients

Full Information

First Posted
August 20, 2007
Last Updated
March 23, 2010
Sponsor
The Center for Rheumatic Disease, Allergy, & Immunology
Collaborators
Saint Luke's Health System
search

1. Study Identification

Unique Protocol Identification Number
NCT00519363
Brief Title
Statins and Lupus: Effects of Statins on Clinical Lupus Parameters, Serological Markers and Toll-like Receptors
Official Title
Statins and Lupus: Effects of Statins on Clinical Lupus Parameters, Serological Markers and Toll-like Receptors.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2009
Overall Recruitment Status
Completed
Study Start Date
September 2007 (undefined)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
The Center for Rheumatic Disease, Allergy, & Immunology
Collaborators
Saint Luke's Health System

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is an open label pilot clinical trial on a cohort of 15 Lupus patients from the Center for Rheumatic Disease. Clinical evaluations and laboratory tests will be done and then if eligible, the patients will receive oral atorvastatin, at a fixed dose of 40mg/day. Statins have been shown to induce clinical improvement in rheumatoid arthritis patients, as well as lupus patients. The effectiveness has been noted within 8 to 14 days, we will do our study for 3 months. Clinical and laboratory tests will be checked at the 1 and 3 month interval. We hypothesize that statin drugs (atorvastatin) slow the progression of SLE(Systemic Lupus Erythematosus) disease activity and down regulates TLR(Toll-like receptors) 2,4,and 9 pathways in addition to lowering lipid levels.
Detailed Description
Atorvastin (Lipitor) is a commonly used drug approved by the FDA for treatment of dyslipidemias. It is a relatively safe drug to use with periodic monitoring. Eligibility critera: age 18-60, females, as a marjority of lupus patients are female at least 4 ACR (American College of Rheumatology) criteria of SLE(Systemic Lupus Erythematosus) Moderate to Severe disease activity using approved SLEDAI(Systemic Lupus Erythematosus Disease Activity Index) LDL cholesterol 100-190mg/dl Exclusion criteria: Pregnancy, and or lactating or wants to get pregnant Unable to take atorvastatin due to allergy, liver disease, elevated liver functions, myositis, or elvated CPK(creatine phosphakinase) already on lipid lowering therapy already on amiodarone, clarithromycin, cyclosporin, erythromycin, itraconazole, ketoconazole, nefazodone, verapamil, protease inhibitors, niacin, digoxin,k cholestyramine, colestipol has a dianosis of Myositis. Our goal is to colledt preliminary data to see if there is a trend for the efficacy of atorvastatin in ameliorating SLE disease activity and to evaluate TLRs(Toll-like receptor) in SLE patients. A p value of <0.05 will be considered statistically significant. Our baseline and at subsequent visits, we will have 80% power to detect a minimum of 34%-39% difference for most of the continous variables measured at different intervals.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Systemic Lupus Erythematosus
Keywords
Lupus, TLR's, Hyperlipidemia, age eighteen to sixty, female with SLE, SLEDAI, greater than four, LDL cholesterol elevated

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
atorvastatin
Other Intervention Name(s)
Lipitor 40mg
Intervention Description
atorvastatin 40mg, given orally daily for 3 months.
Primary Outcome Measure Information:
Title
decrease the SLEDAI level of female lupus patients, down regulate the TLR 2,4, and 9.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
lower lipid levels in female lupus patients
Time Frame
3 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-60, female have at least four ACR criteria for SLE SLEDAI score > 4 LDL cholesterol level from 100-190mg/dl Exclusion Criteria: Pregnant, lactating, or wanting to become pregnant unable to take atorvastatin due to allergy, liver disease, elevated lever function test, myositis, or eleveated CPK already on lipid lowering therapy participating in another lupus study on drugs such as: amiodarone, clarithromycin, clclosporine, erythromycin, itraconazole, ketoconazole, nefazodone, verapamil, protease inhibitors, niacin, digoxin, cholestryrmine, colestipol has a diagnosis of myositis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nabih I Abdou, MD, PhD
Organizational Affiliation
The Center for Rheumatic Disease, Allergy, and Immunology
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Center for Rheumatic Disease, Allergy, and Immunology
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64111
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Statins and Lupus: Effects of Statins on Clinical Lupus Parameters, Serological Markers and Toll-like Receptors

We'll reach out to this number within 24 hrs