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Association Between Chronic Osteomyelitis and Risk of End-Stage Renal Disease: A Nationwide Population-Based Cohort Study

Inflammation, which initiates endothelial dysfunction, vascular atherosclerosis, and oxidative stress, may negatively influence renal function and accelerate the development of end-stage renal disease (ESRD). The role of chronic osteomyelitis (COM), a chronic inflammatory disease, in the development...

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Autores principales: Lin, Shih-Yi, Lin, Cheng-Li, Tseng, Chun-Hung, Chang, Yen-Jung, Wang, I-Kuan, Yeh, Hung-Chieh, Kao, Chia-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504595/
https://www.ncbi.nlm.nih.gov/pubmed/26166123
http://dx.doi.org/10.1097/MD.0000000000001141
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author Lin, Shih-Yi
Lin, Cheng-Li
Tseng, Chun-Hung
Chang, Yen-Jung
Wang, I-Kuan
Yeh, Hung-Chieh
Kao, Chia-Hung
author_facet Lin, Shih-Yi
Lin, Cheng-Li
Tseng, Chun-Hung
Chang, Yen-Jung
Wang, I-Kuan
Yeh, Hung-Chieh
Kao, Chia-Hung
author_sort Lin, Shih-Yi
collection PubMed
description Inflammation, which initiates endothelial dysfunction, vascular atherosclerosis, and oxidative stress, may negatively influence renal function and accelerate the development of end-stage renal disease (ESRD). The role of chronic osteomyelitis (COM), a chronic inflammatory disease, in the development of ESRD has not been investigated. This study explored whether patients with COM have a higher risk of ESRD than that of patients without COM. Taiwan National Health Insurance claims from 1997 to 2010 were used to identify 24,267 newly diagnosed patients with COM and 97,068 age- and sex-matched non-COM controls for comparison. The risks of ESRD among COM patients, with adjustment for comorbidities, namely, hypertension, diabetes, coronary artery disease, congestive heart failure, and hyperlipidemia, were assessed until the end of 2010. ESRD risk was 2.01-fold higher (95% confidence interval [CI]: 1.81–2.25) in the COM cohort than in the non-COM cohort. Regarding the joint effect of COM with comorbidity, the ESRD risk was 1.57-fold higher (95% CI: 1.23–2.00) for the COM cohort without comorbidities and increased to 2.25 (95% CI: 1.97–2.57) for the COM cohort with at least 1 comorbidity. Age-specific analysis revealed that the adjusted ESRD risk for the COM cohort increased as age decreased, with the highest hazard ratio being 17.8 (95% CI: 5.18–61.4) for patients aged 20–34 years. This was the first study to report that COM is associated with an increased risk of ESRD, particularly among patients with comorbidities and younger patients.
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spelling pubmed-45045952015-08-05 Association Between Chronic Osteomyelitis and Risk of End-Stage Renal Disease: A Nationwide Population-Based Cohort Study Lin, Shih-Yi Lin, Cheng-Li Tseng, Chun-Hung Chang, Yen-Jung Wang, I-Kuan Yeh, Hung-Chieh Kao, Chia-Hung Medicine (Baltimore) 5200 Inflammation, which initiates endothelial dysfunction, vascular atherosclerosis, and oxidative stress, may negatively influence renal function and accelerate the development of end-stage renal disease (ESRD). The role of chronic osteomyelitis (COM), a chronic inflammatory disease, in the development of ESRD has not been investigated. This study explored whether patients with COM have a higher risk of ESRD than that of patients without COM. Taiwan National Health Insurance claims from 1997 to 2010 were used to identify 24,267 newly diagnosed patients with COM and 97,068 age- and sex-matched non-COM controls for comparison. The risks of ESRD among COM patients, with adjustment for comorbidities, namely, hypertension, diabetes, coronary artery disease, congestive heart failure, and hyperlipidemia, were assessed until the end of 2010. ESRD risk was 2.01-fold higher (95% confidence interval [CI]: 1.81–2.25) in the COM cohort than in the non-COM cohort. Regarding the joint effect of COM with comorbidity, the ESRD risk was 1.57-fold higher (95% CI: 1.23–2.00) for the COM cohort without comorbidities and increased to 2.25 (95% CI: 1.97–2.57) for the COM cohort with at least 1 comorbidity. Age-specific analysis revealed that the adjusted ESRD risk for the COM cohort increased as age decreased, with the highest hazard ratio being 17.8 (95% CI: 5.18–61.4) for patients aged 20–34 years. This was the first study to report that COM is associated with an increased risk of ESRD, particularly among patients with comorbidities and younger patients. Wolters Kluwer Health 2015-07-13 /pmc/articles/PMC4504595/ /pubmed/26166123 http://dx.doi.org/10.1097/MD.0000000000001141 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 5200
Lin, Shih-Yi
Lin, Cheng-Li
Tseng, Chun-Hung
Chang, Yen-Jung
Wang, I-Kuan
Yeh, Hung-Chieh
Kao, Chia-Hung
Association Between Chronic Osteomyelitis and Risk of End-Stage Renal Disease: A Nationwide Population-Based Cohort Study
title Association Between Chronic Osteomyelitis and Risk of End-Stage Renal Disease: A Nationwide Population-Based Cohort Study
title_full Association Between Chronic Osteomyelitis and Risk of End-Stage Renal Disease: A Nationwide Population-Based Cohort Study
title_fullStr Association Between Chronic Osteomyelitis and Risk of End-Stage Renal Disease: A Nationwide Population-Based Cohort Study
title_full_unstemmed Association Between Chronic Osteomyelitis and Risk of End-Stage Renal Disease: A Nationwide Population-Based Cohort Study
title_short Association Between Chronic Osteomyelitis and Risk of End-Stage Renal Disease: A Nationwide Population-Based Cohort Study
title_sort association between chronic osteomyelitis and risk of end-stage renal disease: a nationwide population-based cohort study
topic 5200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504595/
https://www.ncbi.nlm.nih.gov/pubmed/26166123
http://dx.doi.org/10.1097/MD.0000000000001141
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