Vitamin D Supplementation in Systemic Lupus Erythematosus
- Conditions
- Vitamin D Deficiency
- Registration Number
- NCT01413230
- Lead Sponsor
- Assistance Publique - Hôpitaux de Paris
- Brief Summary
Systemic Lupus Erythematosus (SLE) is a systemic autoimmune disorder. It mainly involves the skin, the joints, the nervous system and the kidney and may be life threatening.
SLE is associated with production of autoantibodies and perturbations in regulatory T cells and T helper lymphocytes producing interleukin (IL)-17 (Th17 cells).
Treatments include corticosteroids, hydroxychloroquine and immunosuppressive agents.
Immunomodulatory effects of vitamin D supplementation in VITRO was recently described, notably the expansion of Treg able to suppress inflammatory responses mediated by CD4+ and CD8+ T cells and the decrease of Th17 cells.
- Detailed Description
Systemic Lupus Erythematosus (SLE) is a systemic autoimmune disorder. It mainly involves the skin, the joints, the nervous system and the kidney and may be life threatening.
SLE is associated with production of autoantibodies and perturbations in regulatory T cells and T helper lymphocytes producing interleukin (IL)-17 (Th17 cells).
Treatments include corticosteroids, hydroxychloroquine and immunosuppressive agents.
Immunomodulatory effects of vitamin D supplementation in VITRO was recently described, notably the expansion of Treg able to suppress inflammatory responses mediated by CD4+ and CD8+ T cells and the decrease of Th17 cells.
Objective : To evaluate the cellular immune response after vitamin D supplementation in patients with SLE.
Methods : This is an open prospective trial. SLE patients with hypovitaminosis D (\< 30 ng/mL) receive vitamin D supplementation. 100 000 UI of cholecalciferol per week for 4 weeks then 100 000 UI of cholecalciferol per month for 6 months will be administered. All patients are followed after the beginning of vitamin D supplementation at month 2 and month 6.
End points :
1. Clinical and biological tolerance: Absence of hypercalcemia or lithiasis during and after vitamin D supplementation.
2. Immunologic follow-up of T cells and B cells homeostasis (including Treg and Th17) and gene expression profile in PBMCs using TRANSCRIPTOMIC analysis, before, during and after vitamin D supplementation.
3. Clinical efficacy: follow-up of clinical manifestations of SLE and disease activity score (SLEDAI) during and after vitamin D supplementation.
Schedule : Duration of patients' inclusion period is estimated 3
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
- Systemic lupus erythematosus
- Age > 18 years
- Serum vitamin D levels [25(OH)D] < 30 ng/mL
- Low to moderate active disease without modification of associated treatments
- Pregnancy
- Serum 25(OH)D levels > 30 ng/mL
- Flare requiring modification of treatments
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Immunologic follow-up of T cells and B cells homeostasis (including regulatory T cells and Th17 cells) and gene expression profile of PBMCs using TRANSCRIPTOMIC analysis, before, during and after vitamin D supplementation 6 months Immunologic follow-up of T cells and B cells homeostasis (including regulatory T cells and Th17 cells) and gene expression profile of PBMCs using TRANSCRIPTOMIC analysis, before, during and after vitamin D supplementation
- Secondary Outcome Measures
Name Time Method Clinical tolerance: Absence of Hypercalcemia and lithiasis during and after vitamin D supplementation 6 months Clinical tolerance: Absence of Hypercalcemia and lithiasis during and after vitamin D supplementation
Clinical efficacy: follow-up of clinical manifestations of SLE and disease activity score (SLEDAI) 6 months Clinical efficacy: follow-up of clinical manifestations of SLE and disease activity score (SLEDAI)
Trial Locations
- Locations (3)
Chu Pitie Salpetriere
🇫🇷Paris, France
Nathalie Costedoat-Chalumeau
🇫🇷Paris, France
Hopital la Pitie Salpétrière
🇫🇷Paris, France