10
IRUS Total
Downloads

Nanoscale mechanisms in age-related hip-fractures

File Description SizeFormat 
s41598-020-69783-5.pdfPublished version2.11 MBAdobe PDFView/Open
Title: Nanoscale mechanisms in age-related hip-fractures
Authors: Ma, S
Goh, EL
Tay, T
Wiles, C
Boughton, O
Churchwell, J
Wu, Y
Karunaratne, A
Bhattacharya, R
Terrill, N
Cobb, J
Hansen, U
Abel, R
Item Type: Journal Article
Abstract: Nanoscale mineralized collagen fibrils may be important determinants of whole-bone mechanical properties and contribute to the risk of age-related fractures. In a cross-sectional study nano-and tissue-level mechanics were compared across trabecular sections from the proximal femora of three groups(n=10 each): ageing non-fractured donors (Controls);untreated fracture patients (Fx-Untreated); bisphosphonate-treated fracture patients (Fx-BisTreated).Collagen fibril, mineral and tissue mechanics were measured using synchrotron X-Ray diffraction,of bone sections under load. Mechanical data were compared across groups, and tissue-level data were regressed against nano. Compared to controls fracture patients exhibited significantly lower critical strain, max strain and normalized strength, with lower peak collagen and mineral strain. Bisphosphonate-treated exhibited the lowest properties. In all three groups, peak mineral strain coincided with maximum tissue strength (i.e. ultimate stress), whilst peak fibril strain occurred afterwards(i.e. higher strain). Tissue strain and strength were positively and strongly correlated with peak fibril and mineral strains. Age-related fractures were associated with lower peak fibril and mineral strain irrespective of treatment. Indicating earlier mineral disengagement and the subsequent onset of fibril sliding is one of the key mechanisms leading to fracture. Treatments for fragility should target collagen-mineral interactions to restore nano-scale strain to that of healthy bone.
Issue Date: 26-Aug-2020
Date of Acceptance: 13-Jul-2020
URI: http://hdl.handle.net/10044/1/81410
DOI: 10.1038/s41598-020-69783-5
ISSN: 2045-2322
Publisher: Nature Publishing Group
Start Page: 1
End Page: 14
Journal / Book Title: Scientific Reports
Volume: 10
Issue: 14208
Copyright Statement: © The Author(s) 2020. Tis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. Te images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Sponsor/Funder: National Osteoporosis Society
Funder's Grant Number: REF: 402
Publication Status: Published
Online Publication Date: 2020-08-26
Appears in Collections:Mechanical Engineering
Department of Surgery and Cancer
Faculty of Medicine
Faculty of Engineering