Cortical bone and fracture risk: The Tromsø Study

Background: The aim of this thesis was to explore the association of the cortical architecture of the proximal femoral shaft with non-vertebral fractures. We tested the hypotheses that: (i) cortical parameters are associated with fracture risk independent of Fracture Risk Assessment Tool (FRAX) or G...

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Published in:Bone
Main Author: Kral, Rita
Format: Doctoral or Postdoctoral Thesis
Language:English
Published: UiT The Arctic University of Norway 2018
Subjects:
Online Access:https://hdl.handle.net/10037/13979
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author Kral, Rita
author_facet Kral, Rita
author_sort Kral, Rita
collection University of Tromsø: Munin Open Research Archive
container_start_page 259
container_title Bone
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description Background: The aim of this thesis was to explore the association of the cortical architecture of the proximal femoral shaft with non-vertebral fractures. We tested the hypotheses that: (i) cortical parameters are associated with fracture risk independent of Fracture Risk Assessment Tool (FRAX) or Garvan estimates, (ii) women with fractures that are unidentified by FRAX but identified by cortical porosity have a different patient profile that contributes to their fracture risk, and (iii) women with type-2 diabetes mellitus (T2DM) have lower bone turnover markers (BTMs) and lower cortical porosity than those without diabetes, and that higher serum glucose level and body mass index (BMI) are associated with lower BTMs and cortical porosity. Methods: We quantified FRAX and Garvan estimates with femoral neck areal bone mineral density (FN aBMD) and femoral subtrochanteric architecture in 211 postmenopausal women, aged 54–94 years, with non-vertebral fractures and 232 controls in a nested case-control study. Results: Paper I: Cortical porosity and thickness were associated with fracture risk independent of FRAX and Garvan estimates. Cortical porosity but not cortical thickness improved the net reclassification of fracture cases compared with FRAX alone but not compared with Garvan. Paper II: Fracture cases unidentified by FRAX but identified by cortical porosity had a patient profile different from fracture cases identified by FRAX. These patients were younger, had a higher FN aBMD, a lower FRAX score, and fewer had a prior fracture, they had higher cortical porosity, thinner cortices, and a larger total bone size than those identified by FRAX alone. Paper III: Women with T2DM had a higher serum glucose, BMI, and subtrochanteric total volumetric BMD but a lower cortical porosity than nondiabetic women. Increasing serum glucose level was associated with lower BTMs and cortical porosity. Increasing BMI was associated with lower BTMs and thicker cortices. Conclusion: These results suggest that cortical porosity was the ...
format Doctoral or Postdoctoral Thesis
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op_doi https://doi.org/10.1016/j.bone.2018.08.018
op_relation Paper I: Kral, R., Osima, M., Borgen, T. T., Vestgaard, R., Richardsen, E., Bjørnerem, Å. (2017). Increased cortical porosity and reduced cortical thickness of the proximal femur are associated with nonvertebral fracture independent of Fracture Risk Assessment Tool and Garvan estimates in postmenopausal women. PLoS ONE 12(9):e0185363. The article is available at http://hdl.handle.net/10037/11902. Paper II: Kral, R., Osima, M., Vestgaard, R., Richardsen, E., Bjørnerem, Å. Women with fracture, unidentified by FRAX, but identified by cortical porosity, have a different patient profile that contribute to fracture risk. (Manuscript). Published version with altered title is available in Bone , 116 (2018) 259-265: https://doi.org/10.1016/j.bone.2018.08.018. Paper III: Osima, M., Kral, R., Borgen, T. T., Høgestøl, I. K., Joakimsen, R. M., Eriksen, E. F., Bjørnerem, Å. (2017). Women with type 2 diabetes mellitus have lower cortical porosity of the proximal femoral shaft using low-resolution CT than nondiabetic women, and increasing glucose is associated with reduced cortical porosity. Bone , 97, 252-260. Also available in https://doi.org/10.1016/j.bone.2017.01.037.
https://hdl.handle.net/10037/13979
op_rights Attribution-NonCommercial-ShareAlike 3.0 Unported (CC BY-NC-SA 3.0)
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spelling ftunivtroemsoe:oai:munin.uit.no:10037/13979 2025-04-13T14:27:36+00:00 Cortical bone and fracture risk: The Tromsø Study Kral, Rita 2018-03-20 https://hdl.handle.net/10037/13979 eng eng UiT The Arctic University of Norway UiT Norges arktiske universitet Paper I: Kral, R., Osima, M., Borgen, T. T., Vestgaard, R., Richardsen, E., Bjørnerem, Å. (2017). Increased cortical porosity and reduced cortical thickness of the proximal femur are associated with nonvertebral fracture independent of Fracture Risk Assessment Tool and Garvan estimates in postmenopausal women. PLoS ONE 12(9):e0185363. The article is available at http://hdl.handle.net/10037/11902. Paper II: Kral, R., Osima, M., Vestgaard, R., Richardsen, E., Bjørnerem, Å. Women with fracture, unidentified by FRAX, but identified by cortical porosity, have a different patient profile that contribute to fracture risk. (Manuscript). Published version with altered title is available in Bone , 116 (2018) 259-265: https://doi.org/10.1016/j.bone.2018.08.018. Paper III: Osima, M., Kral, R., Borgen, T. T., Høgestøl, I. K., Joakimsen, R. M., Eriksen, E. F., Bjørnerem, Å. (2017). Women with type 2 diabetes mellitus have lower cortical porosity of the proximal femoral shaft using low-resolution CT than nondiabetic women, and increasing glucose is associated with reduced cortical porosity. Bone , 97, 252-260. Also available in https://doi.org/10.1016/j.bone.2017.01.037. https://hdl.handle.net/10037/13979 Attribution-NonCommercial-ShareAlike 3.0 Unported (CC BY-NC-SA 3.0) openAccess Copyright 2018 The Author(s) https://creativecommons.org/licenses/by-nc-sa/3.0 VDP::Medisinske Fag: 700::Helsefag: 800 VDP::Medical disciplines: 700::Health sciences: 800 The Tromsø Study Tromsøundersøkelsen Doctoral thesis Doktorgradsavhandling 2018 ftunivtroemsoe https://doi.org/10.1016/j.bone.2018.08.018 2025-03-14T05:17:57Z Background: The aim of this thesis was to explore the association of the cortical architecture of the proximal femoral shaft with non-vertebral fractures. We tested the hypotheses that: (i) cortical parameters are associated with fracture risk independent of Fracture Risk Assessment Tool (FRAX) or Garvan estimates, (ii) women with fractures that are unidentified by FRAX but identified by cortical porosity have a different patient profile that contributes to their fracture risk, and (iii) women with type-2 diabetes mellitus (T2DM) have lower bone turnover markers (BTMs) and lower cortical porosity than those without diabetes, and that higher serum glucose level and body mass index (BMI) are associated with lower BTMs and cortical porosity. Methods: We quantified FRAX and Garvan estimates with femoral neck areal bone mineral density (FN aBMD) and femoral subtrochanteric architecture in 211 postmenopausal women, aged 54–94 years, with non-vertebral fractures and 232 controls in a nested case-control study. Results: Paper I: Cortical porosity and thickness were associated with fracture risk independent of FRAX and Garvan estimates. Cortical porosity but not cortical thickness improved the net reclassification of fracture cases compared with FRAX alone but not compared with Garvan. Paper II: Fracture cases unidentified by FRAX but identified by cortical porosity had a patient profile different from fracture cases identified by FRAX. These patients were younger, had a higher FN aBMD, a lower FRAX score, and fewer had a prior fracture, they had higher cortical porosity, thinner cortices, and a larger total bone size than those identified by FRAX alone. Paper III: Women with T2DM had a higher serum glucose, BMI, and subtrochanteric total volumetric BMD but a lower cortical porosity than nondiabetic women. Increasing serum glucose level was associated with lower BTMs and cortical porosity. Increasing BMI was associated with lower BTMs and thicker cortices. Conclusion: These results suggest that cortical porosity was the ... Doctoral or Postdoctoral Thesis Tromsø University of Tromsø: Munin Open Research Archive Tromsø Bone 116 259 265
spellingShingle VDP::Medisinske Fag: 700::Helsefag: 800
VDP::Medical disciplines: 700::Health sciences: 800
The Tromsø Study
Tromsøundersøkelsen
Kral, Rita
Cortical bone and fracture risk: The Tromsø Study
title Cortical bone and fracture risk: The Tromsø Study
title_full Cortical bone and fracture risk: The Tromsø Study
title_fullStr Cortical bone and fracture risk: The Tromsø Study
title_full_unstemmed Cortical bone and fracture risk: The Tromsø Study
title_short Cortical bone and fracture risk: The Tromsø Study
title_sort cortical bone and fracture risk: the tromsø study
topic VDP::Medisinske Fag: 700::Helsefag: 800
VDP::Medical disciplines: 700::Health sciences: 800
The Tromsø Study
Tromsøundersøkelsen
topic_facet VDP::Medisinske Fag: 700::Helsefag: 800
VDP::Medical disciplines: 700::Health sciences: 800
The Tromsø Study
Tromsøundersøkelsen
url https://hdl.handle.net/10037/13979