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Atopic eczema and fracture risk in adults: A population-based cohort study

BACKGROUND: Limited evidence suggests increased fracture risk in people with atopic eczema. Any link could have substantial effect; atopic eczema is common, and fractures have associated morbidity and mortality. OBJECTIVE: We sought to examine whether atopic eczema is associated with fracture and wh...

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Autores principales: Lowe, Katherine E., Mansfield, Kathryn E., Delmestri, Antonella, Smeeth, Liam, Roberts, Amanda, Abuabara, Katrina, Prieto-Alhambra, Daniel, Langan, Sinéad M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mosby 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014587/
https://www.ncbi.nlm.nih.gov/pubmed/31757515
http://dx.doi.org/10.1016/j.jaci.2019.09.015
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author Lowe, Katherine E.
Mansfield, Kathryn E.
Delmestri, Antonella
Smeeth, Liam
Roberts, Amanda
Abuabara, Katrina
Prieto-Alhambra, Daniel
Langan, Sinéad M.
author_facet Lowe, Katherine E.
Mansfield, Kathryn E.
Delmestri, Antonella
Smeeth, Liam
Roberts, Amanda
Abuabara, Katrina
Prieto-Alhambra, Daniel
Langan, Sinéad M.
author_sort Lowe, Katherine E.
collection PubMed
description BACKGROUND: Limited evidence suggests increased fracture risk in people with atopic eczema. Any link could have substantial effect; atopic eczema is common, and fractures have associated morbidity and mortality. OBJECTIVE: We sought to examine whether atopic eczema is associated with fracture and whether fracture risk varies with eczema severity. METHODS: We performed a matched cohort study set in primary care (Clinical Practice Research Datalink GOLD 1998-2016) and linked hospital admissions data (Hospital Episode Statistics), including adults (≥18 years old) with atopic eczema matched (by age, sex, general practice, and cohort entry date) with up to 5 individuals without eczema. We estimated hazard ratios (HRs) from stratified Cox regression comparing risk of major osteoporotic (hip, pelvis, spine, wrist, and proximal humerus) fractures individually and any fracture in those with and without atopic eczema. RESULTS: We identified 526,808 people with atopic eczema and 2,569,030 people without atopic eczema. Those with eczema had increased risk of hip (HR, 1.10; 99% CI, 1.06-1.14), pelvic (HR, 1.10; 99% CI, 1.02-1.19), spinal (HR, 1.18; 99% CI, 1.10-1.27), and wrist (HR, 1.07; 99% CI, 1.03,-1.11) fractures. We found no evidence of increased proximal humeral (HR, 1.06; 99% CI, 0.97-1.15) fracture risk. Fracture risk increased with increasing eczema severity, with the strongest associations in people with severe eczema (compared with those without) for spinal (HR, 2.09; 99% CI, 1.66-2.65), pelvic (HR, 1.66; 99% CI, 1.26-2.20), and hip (HR, 1.50; 99% CI, 1.30-1.74) fractures. Associations persisted after oral glucocorticoid adjustment. CONCLUSIONS: People with atopic eczema have increased fracture risk, particularly major osteoporotic fractures.
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spelling pubmed-70145872020-02-19 Atopic eczema and fracture risk in adults: A population-based cohort study Lowe, Katherine E. Mansfield, Kathryn E. Delmestri, Antonella Smeeth, Liam Roberts, Amanda Abuabara, Katrina Prieto-Alhambra, Daniel Langan, Sinéad M. J Allergy Clin Immunol Article BACKGROUND: Limited evidence suggests increased fracture risk in people with atopic eczema. Any link could have substantial effect; atopic eczema is common, and fractures have associated morbidity and mortality. OBJECTIVE: We sought to examine whether atopic eczema is associated with fracture and whether fracture risk varies with eczema severity. METHODS: We performed a matched cohort study set in primary care (Clinical Practice Research Datalink GOLD 1998-2016) and linked hospital admissions data (Hospital Episode Statistics), including adults (≥18 years old) with atopic eczema matched (by age, sex, general practice, and cohort entry date) with up to 5 individuals without eczema. We estimated hazard ratios (HRs) from stratified Cox regression comparing risk of major osteoporotic (hip, pelvis, spine, wrist, and proximal humerus) fractures individually and any fracture in those with and without atopic eczema. RESULTS: We identified 526,808 people with atopic eczema and 2,569,030 people without atopic eczema. Those with eczema had increased risk of hip (HR, 1.10; 99% CI, 1.06-1.14), pelvic (HR, 1.10; 99% CI, 1.02-1.19), spinal (HR, 1.18; 99% CI, 1.10-1.27), and wrist (HR, 1.07; 99% CI, 1.03,-1.11) fractures. We found no evidence of increased proximal humeral (HR, 1.06; 99% CI, 0.97-1.15) fracture risk. Fracture risk increased with increasing eczema severity, with the strongest associations in people with severe eczema (compared with those without) for spinal (HR, 2.09; 99% CI, 1.66-2.65), pelvic (HR, 1.66; 99% CI, 1.26-2.20), and hip (HR, 1.50; 99% CI, 1.30-1.74) fractures. Associations persisted after oral glucocorticoid adjustment. CONCLUSIONS: People with atopic eczema have increased fracture risk, particularly major osteoporotic fractures. Mosby 2020-02 /pmc/articles/PMC7014587/ /pubmed/31757515 http://dx.doi.org/10.1016/j.jaci.2019.09.015 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lowe, Katherine E.
Mansfield, Kathryn E.
Delmestri, Antonella
Smeeth, Liam
Roberts, Amanda
Abuabara, Katrina
Prieto-Alhambra, Daniel
Langan, Sinéad M.
Atopic eczema and fracture risk in adults: A population-based cohort study
title Atopic eczema and fracture risk in adults: A population-based cohort study
title_full Atopic eczema and fracture risk in adults: A population-based cohort study
title_fullStr Atopic eczema and fracture risk in adults: A population-based cohort study
title_full_unstemmed Atopic eczema and fracture risk in adults: A population-based cohort study
title_short Atopic eczema and fracture risk in adults: A population-based cohort study
title_sort atopic eczema and fracture risk in adults: a population-based cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014587/
https://www.ncbi.nlm.nih.gov/pubmed/31757515
http://dx.doi.org/10.1016/j.jaci.2019.09.015
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