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Mycophenolate mofetil in children with steroid-dependent and/or frequently relapsing nephrotic syndrome

BACKGROUND: Mycophenolate mofetil (MMF) has emerged as a new agent for treatment of a variety of glomerular diseases. This study examines the safety and efficacy of MMF in treating pediatric patients with steroid-dependent (SD) and/or frequently relapsing (FR) nephrotic syndrome (NS). METHODS: We re...

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Detalles Bibliográficos
Autores principales: Al-Akash, Samhar, Al Makdama, Abdulkarim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089728/
https://www.ncbi.nlm.nih.gov/pubmed/16270759
http://dx.doi.org/10.5144/0256-4947.2005.380
Descripción
Sumario:BACKGROUND: Mycophenolate mofetil (MMF) has emerged as a new agent for treatment of a variety of glomerular diseases. This study examines the safety and efficacy of MMF in treating pediatric patients with steroid-dependent (SD) and/or frequently relapsing (FR) nephrotic syndrome (NS). METHODS: We retrospectively reviewed the medical records of 18 patients with SDNS and/or FRNS treated with MMF for at least 3 months. MMF was used in 11 patients with SDNS (n=10) and FRNS (n=1), including 7 males and 4 females. RESULTS: Mean age at time of diagnosis of NS was 3.3 years (range, 1.1–8.5 years), and at the start of MMF 5.9 years (range, 2.9–10 years). Seven patients had a renal biopsy prior to starting MMF; all had mesangial proliferative glomerulonephritis. Mean follow-up after starting MMF was 12.2 months (range, 4–24 months). Mean MMF dose was 948 mg/m(2)/day (range, 500–1087 mg/m(2)/day). MMF resulted in improvement in 9 of 11 patients, with 8 patients weaned off steroids completely, with a reduction in the mean relapse rate from 4.7 relapses/patient/year (range, 2.4–6) before MMF to 1.05 relapses/patient/year (range, 0–4.5) after MMF therapy (P=0.0001). The relative risk for relapse before MMF was 4.7 (P=0.0002). None of the patients had significant adverse events or intolerance to MMF therapy. CONCLUSION: We conclude that MMF is a safe and effective option for treatment of children with SDNS and/or FRNS.