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Beta-glucans in advanced CKD: role in endotoxaemia and inflammation
BACKGROUND/AIMS: (1–3)-β-D glucans (BG) are cellular components of yeasts and fungi. Elevated blood levels may be an adjunct in diagnosing invasive fungal infection, though can be high in dialysis patients without fungaemia. BG can also induce false positive signals in endotoxin detection assays (Li...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7137517/ https://www.ncbi.nlm.nih.gov/pubmed/32252666 http://dx.doi.org/10.1186/s12882-020-01779-9 |
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author | Wong, Jonathan Zhang, Yonglong Swift, Oscar Finkelman, Malcolm Patidar, Ashish Ramanarayanan, Sivaramakrishnan Vilar, Enric Farrington, Ken |
author_facet | Wong, Jonathan Zhang, Yonglong Swift, Oscar Finkelman, Malcolm Patidar, Ashish Ramanarayanan, Sivaramakrishnan Vilar, Enric Farrington, Ken |
author_sort | Wong, Jonathan |
collection | PubMed |
description | BACKGROUND/AIMS: (1–3)-β-D glucans (BG) are cellular components of yeasts and fungi. Elevated blood levels may be an adjunct in diagnosing invasive fungal infection, though can be high in dialysis patients without fungaemia. BG can also induce false positive signals in endotoxin detection assays (Limulus Amoebocyte Lysate [LAL] assay). We explored the relationship between BG levels, renal impairment, endotoxaemia and inflammation. METHODS: We measured serum BG levels, markers of inflammation and blood endotoxin levels in 20 controls, 20 with stages 1–3 chronic kidney disease (CKD), 20 with stages 4–5 CKD, 15 on peritoneal dialysis (PD) and 60 on haemodialysis (HD). Another 30 patients were studied before and after HD initiation. RESULTS: BG levels increased with advancing CKD, being highest in HD patients, 22% of whom had elevated levels (> 80 pg/ml). Levels increased significantly following HD initiation. Levels also correlated positively with CRP, TNFα, IL-6 levels, independently of CKD stage. Blood endotoxin was detectable by LAL assays in 10–53% of the CKD cohort, being most prevalent in the HD group, and correlating positively with BG levels. Adding BG blocking agent to the assay reduced endotoxin detection confining it to only 5% of HD patients. Levels of inflammatory markers were higher in those with detectable endotoxin - whether false- or true positives. CONCLUSION: BG levels increased with decreasing renal function, being highest in dialysis patients. High BG levels were associated with false positive blood endotoxin signals, and with markers of inflammation, independently of CKD stage. The cause for high BG levels is unknown but could reflect increased gut permeability and altered mononuclear phagocytic system function. |
format | Online Article Text |
id | pubmed-7137517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71375172020-04-11 Beta-glucans in advanced CKD: role in endotoxaemia and inflammation Wong, Jonathan Zhang, Yonglong Swift, Oscar Finkelman, Malcolm Patidar, Ashish Ramanarayanan, Sivaramakrishnan Vilar, Enric Farrington, Ken BMC Nephrol Research Article BACKGROUND/AIMS: (1–3)-β-D glucans (BG) are cellular components of yeasts and fungi. Elevated blood levels may be an adjunct in diagnosing invasive fungal infection, though can be high in dialysis patients without fungaemia. BG can also induce false positive signals in endotoxin detection assays (Limulus Amoebocyte Lysate [LAL] assay). We explored the relationship between BG levels, renal impairment, endotoxaemia and inflammation. METHODS: We measured serum BG levels, markers of inflammation and blood endotoxin levels in 20 controls, 20 with stages 1–3 chronic kidney disease (CKD), 20 with stages 4–5 CKD, 15 on peritoneal dialysis (PD) and 60 on haemodialysis (HD). Another 30 patients were studied before and after HD initiation. RESULTS: BG levels increased with advancing CKD, being highest in HD patients, 22% of whom had elevated levels (> 80 pg/ml). Levels increased significantly following HD initiation. Levels also correlated positively with CRP, TNFα, IL-6 levels, independently of CKD stage. Blood endotoxin was detectable by LAL assays in 10–53% of the CKD cohort, being most prevalent in the HD group, and correlating positively with BG levels. Adding BG blocking agent to the assay reduced endotoxin detection confining it to only 5% of HD patients. Levels of inflammatory markers were higher in those with detectable endotoxin - whether false- or true positives. CONCLUSION: BG levels increased with decreasing renal function, being highest in dialysis patients. High BG levels were associated with false positive blood endotoxin signals, and with markers of inflammation, independently of CKD stage. The cause for high BG levels is unknown but could reflect increased gut permeability and altered mononuclear phagocytic system function. BioMed Central 2020-04-06 /pmc/articles/PMC7137517/ /pubmed/32252666 http://dx.doi.org/10.1186/s12882-020-01779-9 Text en © The Author(s) 2020 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/. 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 in a credit line to the data. |
spellingShingle | Research Article Wong, Jonathan Zhang, Yonglong Swift, Oscar Finkelman, Malcolm Patidar, Ashish Ramanarayanan, Sivaramakrishnan Vilar, Enric Farrington, Ken Beta-glucans in advanced CKD: role in endotoxaemia and inflammation |
title | Beta-glucans in advanced CKD: role in endotoxaemia and inflammation |
title_full | Beta-glucans in advanced CKD: role in endotoxaemia and inflammation |
title_fullStr | Beta-glucans in advanced CKD: role in endotoxaemia and inflammation |
title_full_unstemmed | Beta-glucans in advanced CKD: role in endotoxaemia and inflammation |
title_short | Beta-glucans in advanced CKD: role in endotoxaemia and inflammation |
title_sort | beta-glucans in advanced ckd: role in endotoxaemia and inflammation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7137517/ https://www.ncbi.nlm.nih.gov/pubmed/32252666 http://dx.doi.org/10.1186/s12882-020-01779-9 |
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