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Pamidronate treatment of severe osteogenesis imperfecta in children under 3 years of age.
Plotkin, H; Rauch, F; Bishop, N J; Montpetit, K; Ruck-Gibis, J; Travers, R; Glorieux, F H.
Afiliación
  • Plotkin H; Shriners Hospital for Children, and Department of Surgery, McGill University, Montréal, Québec, Canada.
J Clin Endocrinol Metab ; 85(5): 1846-50, 2000 May.
Article en En | MEDLINE | ID: mdl-10843163
Severe osteogenesis imperfecta (OI) is a hereditary disorder characterized by increased bone fragility and progressive bone deformity. Cyclical pamidronate infusions improve clinical outcome in children older than 3 yr of age with severe OI. Because earlier treatment may have potential to prevent deformities and improve functional prognosis in young children, we studied nine severely affected OI patients under 2 yr of age (2.3-20.7 months at entry) for a period of 12 months. Pamidronate was administered i.v. in cycles of 3 consecutive days. Patients received four to eight cycles during the treatment period, with cumulative doses averaging 12.4 mg/kg. Clinical changes were evaluated regularly during treatment, and radiological changes were assessed after 6-12 months of treatment. The control group consisted of six age-matched, severely affected OI patients, who had not received pamidronate treatment. During treatment bone mineral density (BMD) increased between 86-227%. The deviation from normal, as indicated by the z-score, diminished from -6.5 +/- 2.1 to -3.0 +/- 2.1 (P < 0.001). In the control group the BMD z-score worsened significantly. Vertebral coronal area increased in all treated patients (11.4 +/- 3.4 to 14.9 +/- 1.8 cm2; P < 0.001), but decreased in the untreated group (P < 0.05). In the treated patients, fracture rate was lower than in control patients (2.6 +/- 2.5 vs. 6.3 +/- 1.6 fractures/year; P < 0.01). No adverse side-effects were noted, apart from the well known acute phase reaction during the first infusion cycle. Pamidronate treatment in severely affected OI patients under 3 yr of age is safe, increases BMD, and decreases fracture rate.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta / Densidad Ósea / Difosfonatos Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: J Clin Endocrinol Metab Año: 2000 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta / Densidad Ósea / Difosfonatos Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: J Clin Endocrinol Metab Año: 2000 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos