Osteogenesis imperfecta in childhood: Impairment and disability. a prospective study with 4-year follow-up

Abstract

Engelbert RH, Uiterwall CS, Gerver W-J, van der Net J-J, Pruijs HE, Helders PJ. Osteogenesis imperfecta in childhood: impairment and disability. A prospective study with 4-year follow-up. Arch Phys Med Rehabil 2004;85:772-8. Objectives To study (1) changes in anthropometrics, joint range of motion (ROM), muscle strength, functional ability, caregiver assistance, and level of ambulation in children with osteogenesis imperfecta (OI) and (2) the prediction of clinical characteristics at the level of ambulation at follow-up and the prediction of clinical characteristics on progression or regression at the level of ambulation over time. Design Prospective study with follow-up of 4 years. Setting A children’s hospital that serves a nationwide center for treatment and research in children with OI in the Netherlands. Participants At follow-up, 49 children (24 boys, 25 girls; mean age ± standard deviation, 11.3±3.8y; range, 5.2–19.4y) participated. Interventions Not applicable. Main outcome measures Anthropometry, joint ROM, muscle strength, fracture frequency, intramedullary rodding, level of ambulation, functional ability, and caregiver assistance. Results In type I OI, total joint ROM decreased significantly over time, especially in the lower extremities, with a significant decrease in generalized joint hypermobility according to Bulbena (median start, 7.5; interquartile range [IQR], 4–9; median end, 6; IQR, 2–7; P<.001). In types III and IV, a severe decrease in total joint ROM was present without significant changes over time. No significant changes in total muscle strength (upper or lower extremities) in the different types of OI were measured at follow-up. In OI type I, a significant increase in self-care ( P=.003) and social function ( P=.008) was measured; in type III, a significant increase in self-care ( P=.003), mobility ( P=.004), and social function ( P=.005) was measured, with a significant decrease in parental assistance in self-care ( P=.02) and mobility ( P=.005). In type IV, a significant increase was observed in the self-care ( P=.01) and social function domains ( P=.02). Type of OI (regression coefficient=−1.0; 95% confidence interval [CI], −1.64 to −0.47) and total muscle strength were the only significant predictors for level of ambulation (regression coefficient=.01; 95% CI, .17–.32). Body weight was significantly lower in the group that progressed in level of ambulation ( P=.03), whereas children with a decline in level of ambulation had significantly higher body weight ( P=.05). Conclusions Ours is the first study with a long-term follow-up that provides information concerning the natural course of developmental outcome parameters of OI in childhood. Joint ROM and muscle strength did not change significantly over time, possibly because of the biomechanical skeletal properties of the different OI types. Functional ability improved significantly over time, but, especially in types III and IV, did not reach normative values, possibly because of a plateau phase in functional ability. Knowledge of the natural course of the disease is essential to interpret the results from intervention studies.