Systemic Lupus Erythematosus
Conditions
Keywords
Lupus, TLR's, Hyperlipidemia, age eighteen to sixty, female with SLE, SLEDAI, greater than four, LDL cholesterol elevated
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.
Interventions
atorvastatin 40mg, given orally daily for 3 months.
Sponsors
Study design
Eligibility
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| decrease the SLEDAI level of female lupus patients, down regulate the TLR 2,4, and 9. | 3 months |
Secondary
| Measure | Time frame |
|---|---|
| lower lipid levels in female lupus patients | 3 months |
Countries
United States