Lupus Erythematosus, Systemic Clinical Trial
Official title:
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Test the Safety and Efficacy of Lipitor (Atorvastatin) in Reducing the Progression of Carotid IMT in Early Childhood SLE
The purpose of this study is:
1. To assess the efficacy of a lipid-lowering agent (atorvastatin) on the development of
atherosclerosis that predisposes children with SLE to cardiovascular events in
adulthood.
2. To assess the safety of intermediate-term (36 months) treatment of children and young
adults with atorvastatin.
3. To further characterize the course of SLE in children and young adults, by establishing
a cohort of pediatric SLE patients to be followed prospectively.
4. To establish a mechanism for conducting clinical trials in rare pediatric rheumatic
diseases using the Children's Arthritis and Rheumatology Research Alliance (CARRA).
Children and adolescents with SLE represent 15% of all SLE patients. Children with SLE
suffer high morbidity that affects many organ systems, reduces their quality of life, and
shortens their lifespan. As more children with SLE survive into adulthood, atherosclerotic
cardiovascular disease has emerged as a major concern. SLE is a significant risk factor for
myocardial infarction and death in young premenopausal women with SLE, even after
controlling for traditional cardiovascular risk factors. Acceleration of atherogenesis in
SLE most likely reflects SLE-associated vascular immune and inflammatory changes.
Although limited, the data on cardiovascular and lipid abnormalities in children with SLE
implicate atherosclerosis as an important cause of long-term morbidity and mortality. The
3-hydroxy-3-methlglutaryl-coenzyme A (HMG CoA) reductase inhibitors, or statins, reduce
mortality and morbidity from atherosclerosis in adults and have intrinsic anti-inflammatory
and immune modulatory properties. These anti-inflammatory and immune modulatory activities
may have particular benefit in the prevention and treatment of atherosclerosis in SLE. This
trial will evaluate atorvastatin in children with SLE in the largest cohort of pediatric SLE
patients ever studied prospectively.
Children in this study will be randomized to receive either atorvastatin or a placebo. All
children will be followed for 3 years, during which they will have 15 study visits. Study
visits will generally last 2 hours and will include medical interview, medication review and
pill count, physical examination, and blood and urine tests. Cardiovascular-specific outcome
measures will include assessments of high sensitivity CRP; fasting lipid profile;
homocysteine level; apolipoprotein A, B1, and Lp(a); carotid intima media thickness (IMT);
and tensor diffusion/MRI.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment
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