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The risk of new fragility fractures in patients with chronic kidney disease and hip fracture—a population-based cohort study in the UK

SUMMARY: Chronic kidney disease (CKD) is a risk factor for fractures. However, in hip fracture patients, CKD G3-G5 was associated with a higher mortality risk and not associated with a higher risk of subsequent non-hip fractures compared to eGFR > 60 ml/min. The higher mortality risk may, as comp...

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Autores principales: de Bruin, I.J.A., Wyers, C.E., Souverein, P.C., van Staa, T.P., Geusens, P.P.M.M., van den Bergh, J.P.W., de Vries, F., Driessen, J.H.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360657/
https://www.ncbi.nlm.nih.gov/pubmed/32266436
http://dx.doi.org/10.1007/s00198-020-05351-x
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author de Bruin, I.J.A.
Wyers, C.E.
Souverein, P.C.
van Staa, T.P.
Geusens, P.P.M.M.
van den Bergh, J.P.W.
de Vries, F.
Driessen, J.H.M.
author_facet de Bruin, I.J.A.
Wyers, C.E.
Souverein, P.C.
van Staa, T.P.
Geusens, P.P.M.M.
van den Bergh, J.P.W.
de Vries, F.
Driessen, J.H.M.
author_sort de Bruin, I.J.A.
collection PubMed
description SUMMARY: Chronic kidney disease (CKD) is a risk factor for fractures. However, in hip fracture patients, CKD G3-G5 was associated with a higher mortality risk and not associated with a higher risk of subsequent non-hip fractures compared to eGFR > 60 ml/min. The higher mortality risk may, as competing risk, explain our findings. INTRODUCTION: Chronic kidney disease (CKD) is a known risk factor for fragility fractures. Patients aged 50+ with a recent fragility fracture have an increased risk of subsequent fractures. Our aim was to evaluate the association between CKD stages G3–G5 versus estimated glomerular filtration rate (eGFR) > 60 ml/min and the risk of a new non-hip fracture or fragility fracture in patients with a first hip fracture. METHODS: Population-based cohort study using the UK general practices in the Clinical Practice Research Datalink. Associations between CKD stage and first subsequent fracture were determined using Cox proportional hazard analyses to estimate hazard ratios (HRs). To explore the potential competing risk of mortality, cause-specific (cs) HRs for mortality were estimated. RESULTS: CKD G3–G5 was associated with a lower risk of any subsequent non-hip fracture (HR: 0.90, 95%CI: 0.83–0.97), but not with the risk of subsequent major non-hip fragility fracture. CKD G3-G5 was associated with a higher mortality risk (cs-HR: 1.05, 95%CI: 1.01–1.09). Mortality risk was 1.5- to 3-fold higher in patients with CKD G4 (cs-HR: 1.50, 95%CI: 1.38–1.62) and G5 (cs-HR: 2.93, 95%CI: 2.48–3.46) compared to eGFR > 60 ml/min. CONCLUSIONS: The risk of a subsequent major non-hip fragility fractures following hip fracture was not increased in patients with CKD G3–G5 compared to eGFR > 60 ml/min. Mortality risk was higher in both hip fracture and non-hip fracture patients with CKD G4 and G5. The higher mortality risk may, as competing risk, explain our main finding of no increased or even decreased subsequent fracture risk after a hip fracture in patients with CKD G3–G5. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00198-020-05351-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-73606572020-07-16 The risk of new fragility fractures in patients with chronic kidney disease and hip fracture—a population-based cohort study in the UK de Bruin, I.J.A. Wyers, C.E. Souverein, P.C. van Staa, T.P. Geusens, P.P.M.M. van den Bergh, J.P.W. de Vries, F. Driessen, J.H.M. Osteoporos Int Original Article SUMMARY: Chronic kidney disease (CKD) is a risk factor for fractures. However, in hip fracture patients, CKD G3-G5 was associated with a higher mortality risk and not associated with a higher risk of subsequent non-hip fractures compared to eGFR > 60 ml/min. The higher mortality risk may, as competing risk, explain our findings. INTRODUCTION: Chronic kidney disease (CKD) is a known risk factor for fragility fractures. Patients aged 50+ with a recent fragility fracture have an increased risk of subsequent fractures. Our aim was to evaluate the association between CKD stages G3–G5 versus estimated glomerular filtration rate (eGFR) > 60 ml/min and the risk of a new non-hip fracture or fragility fracture in patients with a first hip fracture. METHODS: Population-based cohort study using the UK general practices in the Clinical Practice Research Datalink. Associations between CKD stage and first subsequent fracture were determined using Cox proportional hazard analyses to estimate hazard ratios (HRs). To explore the potential competing risk of mortality, cause-specific (cs) HRs for mortality were estimated. RESULTS: CKD G3–G5 was associated with a lower risk of any subsequent non-hip fracture (HR: 0.90, 95%CI: 0.83–0.97), but not with the risk of subsequent major non-hip fragility fracture. CKD G3-G5 was associated with a higher mortality risk (cs-HR: 1.05, 95%CI: 1.01–1.09). Mortality risk was 1.5- to 3-fold higher in patients with CKD G4 (cs-HR: 1.50, 95%CI: 1.38–1.62) and G5 (cs-HR: 2.93, 95%CI: 2.48–3.46) compared to eGFR > 60 ml/min. CONCLUSIONS: The risk of a subsequent major non-hip fragility fractures following hip fracture was not increased in patients with CKD G3–G5 compared to eGFR > 60 ml/min. Mortality risk was higher in both hip fracture and non-hip fracture patients with CKD G4 and G5. The higher mortality risk may, as competing risk, explain our main finding of no increased or even decreased subsequent fracture risk after a hip fracture in patients with CKD G3–G5. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00198-020-05351-x) contains supplementary material, which is available to authorized users. Springer London 2020-04-07 2020 /pmc/articles/PMC7360657/ /pubmed/32266436 http://dx.doi.org/10.1007/s00198-020-05351-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Original Article
de Bruin, I.J.A.
Wyers, C.E.
Souverein, P.C.
van Staa, T.P.
Geusens, P.P.M.M.
van den Bergh, J.P.W.
de Vries, F.
Driessen, J.H.M.
The risk of new fragility fractures in patients with chronic kidney disease and hip fracture—a population-based cohort study in the UK
title The risk of new fragility fractures in patients with chronic kidney disease and hip fracture—a population-based cohort study in the UK
title_full The risk of new fragility fractures in patients with chronic kidney disease and hip fracture—a population-based cohort study in the UK
title_fullStr The risk of new fragility fractures in patients with chronic kidney disease and hip fracture—a population-based cohort study in the UK
title_full_unstemmed The risk of new fragility fractures in patients with chronic kidney disease and hip fracture—a population-based cohort study in the UK
title_short The risk of new fragility fractures in patients with chronic kidney disease and hip fracture—a population-based cohort study in the UK
title_sort risk of new fragility fractures in patients with chronic kidney disease and hip fracture—a population-based cohort study in the uk
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360657/
https://www.ncbi.nlm.nih.gov/pubmed/32266436
http://dx.doi.org/10.1007/s00198-020-05351-x
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