Bone robusticity in two distinct skeletal dysplasias diverges from established patterns. Issue 11 (4th May 2017)
- Record Type:
- Journal Article
- Title:
- Bone robusticity in two distinct skeletal dysplasias diverges from established patterns. Issue 11 (4th May 2017)
- Main Title:
- Bone robusticity in two distinct skeletal dysplasias diverges from established patterns
- Authors:
- Citron, Kate
Veneziale, Cosmo
Marino, Josephine
Carter, Erin M.
Jepsen, Karl J.
Raggio, Cathleen - Abstract:
- ABSTRACT: Achondroplasia (ACH) is a heritable disorder of endochondral bone formation characterized by disproportionate short stature. Osteogenesis imperfecta (OI) is a heritable bone and connective tissue disorder characterized by bone fragility. To investigate bone morphology of these groups, we retrospectively reviewed 169 de‐identified bone age films from 20 individuals with ACH, 39 individuals with OI and 37 age‐ and sex‐matched controls (matched to historical measurements from the Bolton–Brush Collection). We calculated robustness (Tt.Ar/Le) and relative cortical area (Ct.Ar/Tt.Ar) from measurements of the second metacarpal, which reflect overall bone health. Relative cortical area (RCA) is a significant predictor of fracture risk and correlates with robustness at other sites. Individuals with OI had RCH values above and robustness values below that of the control population. Bisphosphonate treatment did not significantly impact either robustness or RCA. In contrast to that reported in the unaffected population, there was no sexual dimorphism found in OI robustness or relative cortical area. We suggest that the underlying collagen abnormalities in OI override sex‐specific effects. Individuals with ACH had robustness values above and RCA values below that of the control population. Sexual dimorphism was found in ACH robustness and RCH values. Clinical significance: Identifies morphologic trends in two distinct skeletal dysplasia populations (OI and ACH) to betterABSTRACT: Achondroplasia (ACH) is a heritable disorder of endochondral bone formation characterized by disproportionate short stature. Osteogenesis imperfecta (OI) is a heritable bone and connective tissue disorder characterized by bone fragility. To investigate bone morphology of these groups, we retrospectively reviewed 169 de‐identified bone age films from 20 individuals with ACH, 39 individuals with OI and 37 age‐ and sex‐matched controls (matched to historical measurements from the Bolton–Brush Collection). We calculated robustness (Tt.Ar/Le) and relative cortical area (Ct.Ar/Tt.Ar) from measurements of the second metacarpal, which reflect overall bone health. Relative cortical area (RCA) is a significant predictor of fracture risk and correlates with robustness at other sites. Individuals with OI had RCH values above and robustness values below that of the control population. Bisphosphonate treatment did not significantly impact either robustness or RCA. In contrast to that reported in the unaffected population, there was no sexual dimorphism found in OI robustness or relative cortical area. We suggest that the underlying collagen abnormalities in OI override sex‐specific effects. Individuals with ACH had robustness values above and RCA values below that of the control population. Sexual dimorphism was found in ACH robustness and RCH values. Clinical significance: Identifies morphologic trends in two distinct skeletal dysplasia populations (OI and ACH) to better understand development of bone robusticity and slenderness in humans. Understanding these patterns of bone morphology is important to predict how individuals will respond to treatment and to increase treatment effect. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 35:2392–2396, 2017. … (more)
- Is Part Of:
- Journal of orthopaedic research. Volume 35:Issue 11(2017)
- Journal:
- Journal of orthopaedic research
- Issue:
- Volume 35:Issue 11(2017)
- Issue Display:
- Volume 35, Issue 11 (2017)
- Year:
- 2017
- Volume:
- 35
- Issue:
- 11
- Issue Sort Value:
- 2017-0035-0011-0000
- Page Start:
- 2392
- Page End:
- 2396
- Publication Date:
- 2017-05-04
- Subjects:
- achondroplasia -- osteogenesis imperfecta -- bone robustness -- bone morphology -- bisphosphonate treatment
Orthopedics -- Periodicals
Musculoskeletal system -- Periodicals
616.7 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/jor.23543 ↗
- Languages:
- English
- ISSNs:
- 0736-0266
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5027.665000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5308.xml