OBJECTIVE -The aim of this study was to establish whether type 1 diabetes has a long-term effect on bone development in children and adolescents.RESEARCH DESIGN AND METHODS -Bone characteristics and muscle crosssectional area (CSA) were analyzed cross-sectionally in 41 (19 female and 22 male) patients and were reevaluated after 5.56 Ϯ 0.4 years using peripheral quantitative computed tomography (pQCT). We hypothesize that bone size and muscle mass normalize with age.RESULTS -At the first evaluation, mean Ϯ SD age was 9.87 Ϯ 2.3 years and disease duration was 4.31 Ϯ 2.9 years. Height was Ϫ0.36 Ϯ 1.9 SD, and BMI was 0.39 Ϯ 0.9 SD. Parameters of bone size were low in the whole patient group (corrected for patient's height). At reevaluation, age was 15.44 Ϯ 2.3 years, and patients had a mean height of Ϫ0.12 Ϯ 0.8 SD. BMI SD had increased to 0.57 Ϯ 1.1. Total and cortical CSA had normalized. Those patients with an increase in total CSA had a significant younger age at disease manifestation and a younger age at initial pQCT measurement. Bone size was well adapted to muscle mass expressed as the ratio of bone mineral content per muscle mass, and a close correlation was shown between the increase in bone size and in muscle CSA (r ϭ 0.46, P ϭ 0.03).CONCLUSIONS -Patients with manifestation of type 1 diabetes at an early age had transient impaired bone development. Within the follow-up period, the greatest increase in bone size was found in these patients. In adolescence, all patients had a normal bone size and appropriate adaptation of bone on muscle. There are still no conclusive data on the relative importance of several diabetesspecific characteristics, such as age at onset, disease duration, and glycemic control or insulin regimen, on bone health (6).
Diabetes CareThe majority of earlier studies were cross-sectional using dual-energy X-ray absorptiometry of the spine. In pediatric patients, in particular, this method has l i m i t a t i o n s b e c a u s e o f t h e t w odimensional measurement and therefore height dependency. Longitudinal data on relatively small numbers of patients over 2-4 years revealed disturbed or normal bone development (7,8). A recently published study over a wide time range from 12 to 84 months showed slightly reduced mineralization of the spine independent of metabolic control or microvascular complications (9). The incidence of bone fractures was not increased in a large adult population with type 1 diabetes (10). Therefore, the clinical importance of possibly lower bone mineralization in type 1 diabetes is not clear.The objectives of the present longitudinal study were to evaluate bone mineral density (BMD) and bone size and muscle mass in patients with type 1 diabetes at two time points (5.5 years apart) using peripheral quantitative computed tomography (pQCT). Interpretation of BMD and geometry measurements is incomplete without taking into account muscle mass (11). Therefore, we looked at the ratio between bone mineral content (BMC) and muscle mass (12).
RESEARCH DESIGN ANDMETHODS -In a ...