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Cross-sectional associations between prevalent vertebral fracture and pulmonary function in the sixth Tromsø study

BACKGROUND: Persons with vertebral fracture may have reduced pulmonary function, but this association has not been much studied. The aim of this cross-sectional study was therefore to examine the relationship between vertebral fracture and pulmonary function in a general, elderly population. METHODS...

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Autores principales: Morseth, Bente, Melbye, Hasse, Waterloo, Svanhild, Thomassen, Marte R, Risberg, Marijke J, Emaus, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228451/
https://www.ncbi.nlm.nih.gov/pubmed/24168554
http://dx.doi.org/10.1186/1471-2318-13-116
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author Morseth, Bente
Melbye, Hasse
Waterloo, Svanhild
Thomassen, Marte R
Risberg, Marijke J
Emaus, Nina
author_facet Morseth, Bente
Melbye, Hasse
Waterloo, Svanhild
Thomassen, Marte R
Risberg, Marijke J
Emaus, Nina
author_sort Morseth, Bente
collection PubMed
description BACKGROUND: Persons with vertebral fracture may have reduced pulmonary function, but this association has not been much studied. The aim of this cross-sectional study was therefore to examine the relationship between vertebral fracture and pulmonary function in a general, elderly population. METHODS: Vertebral morphometry was used for vertebral fracture assessment in 2132 elderly men (n = 892) and women (n = 1240) aged 55 to 87 years in the population-based Tromsø Study 2007–08. Pulmonary function was examined by spirometry. Pulmonary function was expressed as FVC% predicted, FEV(1)% predicted, and FEV(1)/FVC% predicted values, adjusted FVC, FEV(1), and FEV(1)/FVC, and obstructive and restrictive ventilatory impairment. Vertebral fracture was classified according to appearance, number, severity, and location of fractures. Associations were analyzed using general linear and logistic models. RESULTS: FVC% predicted and FEV(1)% predicted values were not associated with vertebral fracture (P > 0.05), whereas FEV(1)/FVC% predicted ratio was associated with both prevalent fracture, number of fractures, severity of fractures, and fracture site in men (P < 0.05), but not in women. When FVC, FEV(1), and FEV(1)/FVC values were adjusted for multiple covariates, we found no significant association with vertebral fracture. Obstructive and restrictive ventilatory impairment was not associated with prevalent vertebral fracture. CONCLUSIONS: In conclusion, this study did not confirm any clinically relevant associations between prevalent vertebral fracture and ventilatory impairment in elderly individuals.
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spelling pubmed-42284512014-11-13 Cross-sectional associations between prevalent vertebral fracture and pulmonary function in the sixth Tromsø study Morseth, Bente Melbye, Hasse Waterloo, Svanhild Thomassen, Marte R Risberg, Marijke J Emaus, Nina BMC Geriatr Research Article BACKGROUND: Persons with vertebral fracture may have reduced pulmonary function, but this association has not been much studied. The aim of this cross-sectional study was therefore to examine the relationship between vertebral fracture and pulmonary function in a general, elderly population. METHODS: Vertebral morphometry was used for vertebral fracture assessment in 2132 elderly men (n = 892) and women (n = 1240) aged 55 to 87 years in the population-based Tromsø Study 2007–08. Pulmonary function was examined by spirometry. Pulmonary function was expressed as FVC% predicted, FEV(1)% predicted, and FEV(1)/FVC% predicted values, adjusted FVC, FEV(1), and FEV(1)/FVC, and obstructive and restrictive ventilatory impairment. Vertebral fracture was classified according to appearance, number, severity, and location of fractures. Associations were analyzed using general linear and logistic models. RESULTS: FVC% predicted and FEV(1)% predicted values were not associated with vertebral fracture (P > 0.05), whereas FEV(1)/FVC% predicted ratio was associated with both prevalent fracture, number of fractures, severity of fractures, and fracture site in men (P < 0.05), but not in women. When FVC, FEV(1), and FEV(1)/FVC values were adjusted for multiple covariates, we found no significant association with vertebral fracture. Obstructive and restrictive ventilatory impairment was not associated with prevalent vertebral fracture. CONCLUSIONS: In conclusion, this study did not confirm any clinically relevant associations between prevalent vertebral fracture and ventilatory impairment in elderly individuals. BioMed Central 2013-10-29 /pmc/articles/PMC4228451/ /pubmed/24168554 http://dx.doi.org/10.1186/1471-2318-13-116 Text en Copyright © 2013 Morseth et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Morseth, Bente
Melbye, Hasse
Waterloo, Svanhild
Thomassen, Marte R
Risberg, Marijke J
Emaus, Nina
Cross-sectional associations between prevalent vertebral fracture and pulmonary function in the sixth Tromsø study
title Cross-sectional associations between prevalent vertebral fracture and pulmonary function in the sixth Tromsø study
title_full Cross-sectional associations between prevalent vertebral fracture and pulmonary function in the sixth Tromsø study
title_fullStr Cross-sectional associations between prevalent vertebral fracture and pulmonary function in the sixth Tromsø study
title_full_unstemmed Cross-sectional associations between prevalent vertebral fracture and pulmonary function in the sixth Tromsø study
title_short Cross-sectional associations between prevalent vertebral fracture and pulmonary function in the sixth Tromsø study
title_sort cross-sectional associations between prevalent vertebral fracture and pulmonary function in the sixth tromsø study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228451/
https://www.ncbi.nlm.nih.gov/pubmed/24168554
http://dx.doi.org/10.1186/1471-2318-13-116
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