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Effect of chronic kidney disease on all-cause mortality in tuberculosis disease: an Australian cohort study
BACKGROUND: While there has been a recent epidemiological and clinical focus on the interaction between diabetes and tuberculosis, the interaction between chronic kidney disease and tuberculosis has been less studied. In particular, little is known of the effect of eGFR levels well above that seen i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8812263/ https://www.ncbi.nlm.nih.gov/pubmed/35109801 http://dx.doi.org/10.1186/s12879-022-07039-5 |
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author | Carr, Beau Z. Briganti, Esther M. Musemburi, Joseph Jenkin, Grant A. Denholm, Justin T. |
author_facet | Carr, Beau Z. Briganti, Esther M. Musemburi, Joseph Jenkin, Grant A. Denholm, Justin T. |
author_sort | Carr, Beau Z. |
collection | PubMed |
description | BACKGROUND: While there has been a recent epidemiological and clinical focus on the interaction between diabetes and tuberculosis, the interaction between chronic kidney disease and tuberculosis has been less studied. In particular, little is known of the effect of eGFR levels well above that seen in end stage kidney disease on mortality. METHODS: We conducted a retrospective cohort study of 653 adults from a large Australian hospital network, using data from a state-wide registry of reported tuberculosis cases between 2010 and 2018, with ascertainment of diabetes status and renal function data from hospital medical records and laboratory data. Cox proportional hazards regression models were used to calculate hazard ratios for all-cause mortality associated with categories of chronic kidney disease in adults with tuberculosis disease. RESULTS: Total number of deaths was 25 (3.8%). Compared to tuberculosis cases with eGFR ≥ 60 ml/min, all-cause mortality was higher for those with chronic kidney disease from an eGFR level of 45 ml/min. The association was independent of sex, age and diabetes status with adjusted hazard ratio of 4.6 (95% CI: 1.5, 14.4) for eGFR 30–44 ml/min and 8.3 (95% CI: 2.9, 23.7) for eGFR < 30 ml/min. CONCLUSIONS: Our results suggest a notably increased risk of all-cause mortality even in those with more moderate degrees of renal impairment, in a low tuberculosis prevalence setting. The impact of these findings on a population basis are at least as significant as that found with diabetes and warrant further investigation in populations with higher tuberculosis prevalence. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07039-5. |
format | Online Article Text |
id | pubmed-8812263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88122632022-02-07 Effect of chronic kidney disease on all-cause mortality in tuberculosis disease: an Australian cohort study Carr, Beau Z. Briganti, Esther M. Musemburi, Joseph Jenkin, Grant A. Denholm, Justin T. BMC Infect Dis Research BACKGROUND: While there has been a recent epidemiological and clinical focus on the interaction between diabetes and tuberculosis, the interaction between chronic kidney disease and tuberculosis has been less studied. In particular, little is known of the effect of eGFR levels well above that seen in end stage kidney disease on mortality. METHODS: We conducted a retrospective cohort study of 653 adults from a large Australian hospital network, using data from a state-wide registry of reported tuberculosis cases between 2010 and 2018, with ascertainment of diabetes status and renal function data from hospital medical records and laboratory data. Cox proportional hazards regression models were used to calculate hazard ratios for all-cause mortality associated with categories of chronic kidney disease in adults with tuberculosis disease. RESULTS: Total number of deaths was 25 (3.8%). Compared to tuberculosis cases with eGFR ≥ 60 ml/min, all-cause mortality was higher for those with chronic kidney disease from an eGFR level of 45 ml/min. The association was independent of sex, age and diabetes status with adjusted hazard ratio of 4.6 (95% CI: 1.5, 14.4) for eGFR 30–44 ml/min and 8.3 (95% CI: 2.9, 23.7) for eGFR < 30 ml/min. CONCLUSIONS: Our results suggest a notably increased risk of all-cause mortality even in those with more moderate degrees of renal impairment, in a low tuberculosis prevalence setting. The impact of these findings on a population basis are at least as significant as that found with diabetes and warrant further investigation in populations with higher tuberculosis prevalence. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07039-5. BioMed Central 2022-02-02 /pmc/articles/PMC8812263/ /pubmed/35109801 http://dx.doi.org/10.1186/s12879-022-07039-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Carr, Beau Z. Briganti, Esther M. Musemburi, Joseph Jenkin, Grant A. Denholm, Justin T. Effect of chronic kidney disease on all-cause mortality in tuberculosis disease: an Australian cohort study |
title | Effect of chronic kidney disease on all-cause mortality in tuberculosis disease: an Australian cohort study |
title_full | Effect of chronic kidney disease on all-cause mortality in tuberculosis disease: an Australian cohort study |
title_fullStr | Effect of chronic kidney disease on all-cause mortality in tuberculosis disease: an Australian cohort study |
title_full_unstemmed | Effect of chronic kidney disease on all-cause mortality in tuberculosis disease: an Australian cohort study |
title_short | Effect of chronic kidney disease on all-cause mortality in tuberculosis disease: an Australian cohort study |
title_sort | effect of chronic kidney disease on all-cause mortality in tuberculosis disease: an australian cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8812263/ https://www.ncbi.nlm.nih.gov/pubmed/35109801 http://dx.doi.org/10.1186/s12879-022-07039-5 |
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