We aimed to describe the longitudinal changes in bone mineral content and influencing factors, in children with cystic fibrosis (CF). One hundred children (50 females) had dual X-ray absorptiometry (DXA) performed. Of these, 48 and 24 children had two to three scans, respectively over 10 years of follow-up. DXA data were expressed as lumbar spine bone mineral content standard deviation score (LSBMCSDS) adjusted for age, gender, ethnicity and bone area. Markers of disease, anthropometry and bone biochemistry were collected retrospectively. Baseline LSBMCSDS was >0.5 SDS in 13% children, between -0.5; 0.5 SDS, in 50% and ≤-0.5 in the remainder. Seventy-eight percent of the children who had baseline LSBMCSDS >-0.5, and 35% of the children with poor baseline (LSBMCSDS
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Chirita-Emandi, A., Shepherd, S., Kyriakou, A., Mcneilly, J. D., Dryden, C., Corrigan, D., … Ahmed, S. F. (2017). A retrospective analysis of longitudinal changes in bone mineral content in cystic fibrosis. Journal of Pediatric Endocrinology and Metabolism, 30(8), 807–814. https://doi.org/10.1515/jpem-2016-0057
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