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Development of tibia & fibula bone deficits in children with neurofibromatosis type I - A longitudinal case-control
Alex Ireland1, Amy Riddell2, Ann Prentice3
1Musculoskeletal Science and Sports Medicine Research Centre, Department of Life Sciences, Manchester Metropolitan University, Manchester, UK.
Insights
Children with Neurofibromatosis type 1 (NF1) experience slower bone accrual, leading to progressive lower limb bone deficits. These deficits are partly linked to reduced growth and body weight, suggesting physical activity interventions may help.
Area of Science:
- Pediatric Endocrinology
- Bone Biology
- Genetics
Background:
- Neurofibromatosis type 1 (NF1) is linked to reduced bone mass and increased fracture risk.
- Children with NF1 often exhibit growth deficiencies starting in mid-childhood.
- Tibia bone development and the influence of body size in children with NF1 remain under-explored.
Purpose of the Study:
- To investigate tibia and fibula bone development in children with NF1 throughout childhood.
- To determine the role of body size in bone development among children with NF1.
- To compare bone characteristics between children with and without NF1.
Main Methods:
- Recruited 24 children with NF1 and 104 controls.
- Assessed tibia and fibula bone characteristics using peripheral quantitative computed tomography (pQCT).
- Conducted longitudinal scans over 3.4 years for NF1 group and 1.1 years for controls, using linear mixed effects models.
Main Results:
- Children with NF1 showed a slower rate of tibia and fibula bone mass accrual at all measured sites.
- These differences were partially attenuated (25-50%) when adjusted for height and weight Z-scores.
- Bone mass deficits in NF1 were associated with slower trabecular bone mineral density (BMD) accrual and poorer cortical bone accrual.
Conclusions:
- Lower limb bone deficits in children with NF1 are progressive and evident from mid-childhood.
- These deficits are partly related to impaired longitudinal growth and body weight development in NF1.
- Interventions focused on muscle development or physical activity may help mitigate bone mass accrual deficits in children with NF1.
Abstract:
Neurofibromatosis type 1 (NF1) is associated with lower bone mass and increased risk of fracture. Children with NF1 display faltering growth from mid-childhood. However, to date tibia bone development in children with NF1 across childhood and the role of body size have not been explored. Therefore, we recruited 24 children with NF1 (12 girls, mean age 8.2 ± 1.1y) and 104 children without NF1 (52 girls, mean age 11 ± 1.7y). Tibia and fibula bone characteristics were assessed at 4% and 38% distal-proximal tibia length in all children at baseline using peripheral quantitative computed tomography (pQCT). Longitudinal scans were obtained in 21 children with NF1 (12 girls) over 3.4 ± 0.3y and 71 children without NF1 (34 girls) over 1.1 ± 0.1y, such that at follow-up mean age of both groups (NF1 10.9 ± 1.3y, controls 11.4 ± 1.4y) were similar. Effects of group (NF1/control) on bone outcomes as well as group-by-age interactions, indicating differences in rate of change in bone outcome bone outcomes were assessed via linear mixed effects models with adjustment for sex, age, pubertal status and in additional models with adjustment for height and weight Z-scores. Group (NF1/control)-by-age interactions indicated a slower rate of tibia and fibula bone mass accrual in children with NF1 at all measured sites. These associations were attenuated by 25-50% by adjustment for height and weight Z-scores. At the 4% site, deficits in bone mass at older ages were related to slower trabecular BMD accrual. At the 38% site, group-by-age interactions suggested that bone mass deficits resulted from poorer accrual of cortical CSA and to a lesser extent cortical BMD. Lower limb bone mass deficits evident in children with NF1 appear to be progressive and emerge in mid-childhood. In part, they are related to development of a similar pattern of deficits in longitudinal growth and body weight in NF1. Interventions promoting muscle development or physical activity may be partially effective in attenuating bone mass accrual deficits in this population.
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