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Procalcitonin as a Marker of Comorbid Atrial Fibrillation in Chronic Kidney Disease and History of Sepsis

Cardiovascular disease and infection are the leading causes of mortality in patients with stage 5 chronic kidney disease on hemodialysis (CKD5-HD). Inflammation is a large component in the pathogenesis of both atrial fibrillation (AF) and sepsis and may link these conditions in CKD5-HD. Procalcitoni...

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Autores principales: Bontekoe, Jack, Bansal, Vinod, Lee, Justin, Syed, Mushabbar, Hoppensteadt, Debra, Maia, Paula, Walborn, Amanda, Liles, Jeffrey, Vasaiwala, Smit, Fareed, Jawed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427007/
https://www.ncbi.nlm.nih.gov/pubmed/32539447
http://dx.doi.org/10.1177/1076029620932228
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author Bontekoe, Jack
Bansal, Vinod
Lee, Justin
Syed, Mushabbar
Hoppensteadt, Debra
Maia, Paula
Walborn, Amanda
Liles, Jeffrey
Vasaiwala, Smit
Fareed, Jawed
author_facet Bontekoe, Jack
Bansal, Vinod
Lee, Justin
Syed, Mushabbar
Hoppensteadt, Debra
Maia, Paula
Walborn, Amanda
Liles, Jeffrey
Vasaiwala, Smit
Fareed, Jawed
author_sort Bontekoe, Jack
collection PubMed
description Cardiovascular disease and infection are the leading causes of mortality in patients with stage 5 chronic kidney disease on hemodialysis (CKD5-HD). Inflammation is a large component in the pathogenesis of both atrial fibrillation (AF) and sepsis and may link these conditions in CKD5-HD. Procalcitonin (PCT) is an inflammatory biomarker elevated in systemic infection and CKD5-HD, yet its value with regard to comorbid AF has not been thoroughly investigated. The aim of this study sought to evaluate circulating inflammatory markers, including PCT, Angiopoietin-1, Angiopoetin-2, CD40-L, C-reactive protein, d-dimer, and von Willebrand factor in relation to these conditions. Plasma levels of inflammatory markers were measured by enzyme linked immunosorbent assay method in CKD5-HD (n = 97) patients and controls (n = 50). Procalcitonin levels were significantly elevated (P = .0270) in CKD5-HD with comorbid AF compared to those without AF. Further analysis of patients with a history of sepsis demonstrated significantly elevated levels of PCT (P = .0405) in those with comorbid AF (160.7 ± 39.5 pg/mL) compared to those without AF (117.4 ± 25.3 pg/mL). This study demonstrates that the inflammatory biomarker PCT is further elevated in the presence of both AF and a history of sepsis in hemodialysis patients and suggests that underlying chronic inflammation following sepsis resolution may place these patients at greater risk of developing AF.
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spelling pubmed-74270072020-08-25 Procalcitonin as a Marker of Comorbid Atrial Fibrillation in Chronic Kidney Disease and History of Sepsis Bontekoe, Jack Bansal, Vinod Lee, Justin Syed, Mushabbar Hoppensteadt, Debra Maia, Paula Walborn, Amanda Liles, Jeffrey Vasaiwala, Smit Fareed, Jawed Clin Appl Thromb Hemost Original Article Cardiovascular disease and infection are the leading causes of mortality in patients with stage 5 chronic kidney disease on hemodialysis (CKD5-HD). Inflammation is a large component in the pathogenesis of both atrial fibrillation (AF) and sepsis and may link these conditions in CKD5-HD. Procalcitonin (PCT) is an inflammatory biomarker elevated in systemic infection and CKD5-HD, yet its value with regard to comorbid AF has not been thoroughly investigated. The aim of this study sought to evaluate circulating inflammatory markers, including PCT, Angiopoietin-1, Angiopoetin-2, CD40-L, C-reactive protein, d-dimer, and von Willebrand factor in relation to these conditions. Plasma levels of inflammatory markers were measured by enzyme linked immunosorbent assay method in CKD5-HD (n = 97) patients and controls (n = 50). Procalcitonin levels were significantly elevated (P = .0270) in CKD5-HD with comorbid AF compared to those without AF. Further analysis of patients with a history of sepsis demonstrated significantly elevated levels of PCT (P = .0405) in those with comorbid AF (160.7 ± 39.5 pg/mL) compared to those without AF (117.4 ± 25.3 pg/mL). This study demonstrates that the inflammatory biomarker PCT is further elevated in the presence of both AF and a history of sepsis in hemodialysis patients and suggests that underlying chronic inflammation following sepsis resolution may place these patients at greater risk of developing AF. SAGE Publications 2020-06-15 /pmc/articles/PMC7427007/ /pubmed/32539447 http://dx.doi.org/10.1177/1076029620932228 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Bontekoe, Jack
Bansal, Vinod
Lee, Justin
Syed, Mushabbar
Hoppensteadt, Debra
Maia, Paula
Walborn, Amanda
Liles, Jeffrey
Vasaiwala, Smit
Fareed, Jawed
Procalcitonin as a Marker of Comorbid Atrial Fibrillation in Chronic Kidney Disease and History of Sepsis
title Procalcitonin as a Marker of Comorbid Atrial Fibrillation in Chronic Kidney Disease and History of Sepsis
title_full Procalcitonin as a Marker of Comorbid Atrial Fibrillation in Chronic Kidney Disease and History of Sepsis
title_fullStr Procalcitonin as a Marker of Comorbid Atrial Fibrillation in Chronic Kidney Disease and History of Sepsis
title_full_unstemmed Procalcitonin as a Marker of Comorbid Atrial Fibrillation in Chronic Kidney Disease and History of Sepsis
title_short Procalcitonin as a Marker of Comorbid Atrial Fibrillation in Chronic Kidney Disease and History of Sepsis
title_sort procalcitonin as a marker of comorbid atrial fibrillation in chronic kidney disease and history of sepsis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427007/
https://www.ncbi.nlm.nih.gov/pubmed/32539447
http://dx.doi.org/10.1177/1076029620932228
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