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Complement C3 and incident hospitalization due to chronic kidney disease: a population-based cohort study
BACKGROUND: Circulating C3 has been associated with diabetes and hypertension, which are the leading causes of chronic kidney disease (CKD). C3 activation is considered to contribute to several renal diseases. Here we examined whether elevated C3 concentration is associated with hospitalization due...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383246/ https://www.ncbi.nlm.nih.gov/pubmed/30791918 http://dx.doi.org/10.1186/s12882-019-1248-7 |
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author | Bao, Xue Borné, Yan Muhammad, Iram Faqir Schulz, Christina-Alexandra Persson, Margaretha Orho-Melander, Marju Niu, Kaijun Christensson, Anders Engström, Gunnar |
author_facet | Bao, Xue Borné, Yan Muhammad, Iram Faqir Schulz, Christina-Alexandra Persson, Margaretha Orho-Melander, Marju Niu, Kaijun Christensson, Anders Engström, Gunnar |
author_sort | Bao, Xue |
collection | PubMed |
description | BACKGROUND: Circulating C3 has been associated with diabetes and hypertension, which are the leading causes of chronic kidney disease (CKD). C3 activation is considered to contribute to several renal diseases. Here we examined whether elevated C3 concentration is associated with hospitalization due to CKD in the general population, and whether this relationship is mediated by factors such as diabetes and hypertension. METHODS: Baseline plasma C3 was quantified in 4552 participants, without previous hospital admission due to CKD, from the Malmö Diet and Cancer cohort study. Incidence of first hospitalization due to CKD (main diagnosis) was investigated in relation to C3 levels using Cox proportional hazards regression models after a mean follow-up of 19.2 ± 4.16 years. Traditional risk factors of CKD including diabetes, blood pressure, C-reactive protein and baseline renal function were considered in adjustments and sensitivity analyses. RESULTS: During the follow-up period, 94 subjects were admitted to hospital due to CKD. After multivariate adjustment, the hazard ratios (95% confidence interval) for hospitalization from CKD across quartiles of C3 were 1.00 (reference), 1.68 (0.69, 4.13), 2.71 (1.15, 6.39), and 3.16 (1.36, 7.34) (p for trend = 0.003). Results were generally consistent across different sensitivity analyses. CONCLUSIONS: These findings indicate that C3 is associated with incidence of first hospitalization due to CKD in the general population. The observed relationship cannot be entirely attributed to hyperglycemia and hypertension. |
format | Online Article Text |
id | pubmed-6383246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63832462019-03-01 Complement C3 and incident hospitalization due to chronic kidney disease: a population-based cohort study Bao, Xue Borné, Yan Muhammad, Iram Faqir Schulz, Christina-Alexandra Persson, Margaretha Orho-Melander, Marju Niu, Kaijun Christensson, Anders Engström, Gunnar BMC Nephrol Research Article BACKGROUND: Circulating C3 has been associated with diabetes and hypertension, which are the leading causes of chronic kidney disease (CKD). C3 activation is considered to contribute to several renal diseases. Here we examined whether elevated C3 concentration is associated with hospitalization due to CKD in the general population, and whether this relationship is mediated by factors such as diabetes and hypertension. METHODS: Baseline plasma C3 was quantified in 4552 participants, without previous hospital admission due to CKD, from the Malmö Diet and Cancer cohort study. Incidence of first hospitalization due to CKD (main diagnosis) was investigated in relation to C3 levels using Cox proportional hazards regression models after a mean follow-up of 19.2 ± 4.16 years. Traditional risk factors of CKD including diabetes, blood pressure, C-reactive protein and baseline renal function were considered in adjustments and sensitivity analyses. RESULTS: During the follow-up period, 94 subjects were admitted to hospital due to CKD. After multivariate adjustment, the hazard ratios (95% confidence interval) for hospitalization from CKD across quartiles of C3 were 1.00 (reference), 1.68 (0.69, 4.13), 2.71 (1.15, 6.39), and 3.16 (1.36, 7.34) (p for trend = 0.003). Results were generally consistent across different sensitivity analyses. CONCLUSIONS: These findings indicate that C3 is associated with incidence of first hospitalization due to CKD in the general population. The observed relationship cannot be entirely attributed to hyperglycemia and hypertension. BioMed Central 2019-02-21 /pmc/articles/PMC6383246/ /pubmed/30791918 http://dx.doi.org/10.1186/s12882-019-1248-7 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Bao, Xue Borné, Yan Muhammad, Iram Faqir Schulz, Christina-Alexandra Persson, Margaretha Orho-Melander, Marju Niu, Kaijun Christensson, Anders Engström, Gunnar Complement C3 and incident hospitalization due to chronic kidney disease: a population-based cohort study |
title | Complement C3 and incident hospitalization due to chronic kidney disease: a population-based cohort study |
title_full | Complement C3 and incident hospitalization due to chronic kidney disease: a population-based cohort study |
title_fullStr | Complement C3 and incident hospitalization due to chronic kidney disease: a population-based cohort study |
title_full_unstemmed | Complement C3 and incident hospitalization due to chronic kidney disease: a population-based cohort study |
title_short | Complement C3 and incident hospitalization due to chronic kidney disease: a population-based cohort study |
title_sort | complement c3 and incident hospitalization due to chronic kidney disease: a population-based cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383246/ https://www.ncbi.nlm.nih.gov/pubmed/30791918 http://dx.doi.org/10.1186/s12882-019-1248-7 |
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