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Modern approach to children with osteogenesis imperfecta

Zeitlin, Leonid; Fassier, François; Glorieux, Francis H.

Journal of Pediatric Orthopaedics B: March 2003 - Volume 12 - Issue 2 - p 77-87
OSTEOGENESIS IMPERFECTA
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Osteogenesis Imperfecta (OI) is characterized by bone fragility. At least seven discrete types have been described ranging from mild disease to a lethal form. In a large number of cases, mutations in one of the two genes encoding type I collagen have been found. In forms recently described (types V, VI, VII), such mutations have been excluded. In two other forms, (Bruck, and osteoporosis – pseudoglioma syndromes) defects in other proteins have been characterized. In OI, bone fragility stems from: decreased bone mass, disturbed organization of bone tissue, and altered bone geometry (size and shape). Histologic studies have shown that increased bone turnover is the rule in OI bone. This justifies using bisphosphonates in order to reduce osteoclast mediated bone resorption. Initial results are encouraging. Cyclical intravenous pamidronate administration reduces bone pain and fracture incidence, and increases bone density and level of ambulation, with minimal side effects. Effects on bone include increase in size of vertebral bodies and thickening of cortical bone. These results allow for more efficacious corrective surgery using intramedullary rodding of the long bones and paravertegral instrumentation. Specific occupational and physiotherapy programs are integral parts of the treatment protocol. This multidisciplinary approach will prevail until strategies aiming at the correction of the basic defect(s) will have come to fruition.

Shriners Hospital for Children and McGill University, Montréal, Québec, Canada

Correspondence and requests for reprints to Francis H. Glorieux, Genetics Unit, Shriners Hospital for Children, 1529 Cedar Avenue, Montréal, Québec, Canada H3G 1A6.

Tel: +1 514 842 5964; fax: +1 514 842 5581;

e-mail: glorieux@shriners.mcgill.ca

© 2003 Lippincott Williams & Wilkins, Inc.