Peripheral quantitative computed tomography detects differences at the radius in prepubertal children with cystic fibrosis compared to healthy controls
- PMID: 29324908
- PMCID: PMC5764746
- DOI: 10.1371/journal.pone.0191013
Peripheral quantitative computed tomography detects differences at the radius in prepubertal children with cystic fibrosis compared to healthy controls
Abstract
Introduction: In 2015, 11.9% of people with cystic fibrosis (CF) in the United States had osteopenia, 5.1% osteoporosis, and 0.3% experienced a fracture. Screening for CF-related bone disease starts in childhood, and dual energy x-ray absorptiometry (DXA) is the recommended method. It is unknown whether peripheral quantitative computed tomography (pQCT) can detect deficits earlier than DXA. This study compared pQCT and DXA scans in a group of pre-pubertal children with CF and healthy controls.
Methods: This was a cross-sectional study of children at Tanner stage 1. A pQCT scan of the radius at proximal and distal sites was performed plus a total body DXA scan. Serum C-reactive protein, interleukin-6 and tumor necrosis factor-alpha were also measured.
Results: A total of 34 subjects completed the study; 14 with CF and 20 controls. At the distal radius, pQCT showed a lower total bone mineral density (BMD) Z-score for the CF group (P = 0.01 and P = 0.03 for 2 different reference databases) compared to controls. At the proximal site, the polar strength-strain index was lower in the CF group (P = 0.017). Finally, the total body BMD Z-score by DXA was lower in the CF group, although it did not meet the definition of reduced bone density (P = 0.004). Biomarkers of inflammation were not different.
Conclusions: In this group of pre-pubertal children with CF, measures of bone strength and density by both pQCT and DXA were reduced compared to healthy controls.
Conflict of interest statement
References
-
- Aris RM, Merkel PA, Bachrach LK, Borowitz DS, Boyle MP, Elkin SL, et al. Guide to bone health and disease in cystic fibrosis. J Clin Endocrinol Metab. 2005;90(3):1888–96. doi: 10.1210/jc.2004-1629 - DOI - PubMed
-
- Cystic Fibrosis Foundation 2015 Patient Registry Annual Data Report. Bethesda, MD: Cystic Fibrosis Foundation; 2016.
-
- Louis O, Clerinx P, Gies I, De Wachter E, De Schepper J. Well-nourished cystic fibrosis patients have normal mineral density, but reduced cortical thickness at the forearm. Osteoporos Int. 2009;20(2):309–14. doi: 10.1007/s00198-008-0646-7 - DOI - PubMed
-
- Brookes DS, Briody JN, Munns CF, Davies PS, Hill RJ. Cystic fibrosis-related bone disease in children: Examination of peripheral quantitative computed tomography (pQCT) data. J Cyst Fibros. 2015;14(5):668–77. doi: 10.1016/j.jcf.2015.04.005 - DOI - PubMed
-
- Greulich WW, Pyle SI. Radiographic atlas of skeletal development of the hand and wrist Second edition Stanford University Press, Stanford; 1959.
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