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Extracellular vesicle Cystatin C and CD14 are associated with both renal dysfunction and heart failure

AIMS: Extracellular vesicles (EVs) are small double‐membrane plasma vesicles that play key roles in cellular crosstalk and mechanisms such as inflammation. The role of EVs in combined organ failure such as cardiorenal syndrome has not been investigated. The aim of this study is to identify EV protei...

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Autores principales: Verbree‐Willemsen, Laura, Zhang, Ya‐nan, Ibrahim, Irwani, Ooi, Shirley B.S., Wang, Jiong‐Wei, Mazlan, Muhammad I., Kuan, Win S., Chan, Siew‐Pang, Peelen, Linda M., Grobbee, Diederick E., Richards, A. Mark, Lam, Carolyn S.P., de Kleijn, Dominique P.V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524227/
https://www.ncbi.nlm.nih.gov/pubmed/32648717
http://dx.doi.org/10.1002/ehf2.12699
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author Verbree‐Willemsen, Laura
Zhang, Ya‐nan
Ibrahim, Irwani
Ooi, Shirley B.S.
Wang, Jiong‐Wei
Mazlan, Muhammad I.
Kuan, Win S.
Chan, Siew‐Pang
Peelen, Linda M.
Grobbee, Diederick E.
Richards, A. Mark
Lam, Carolyn S.P.
de Kleijn, Dominique P.V.
author_facet Verbree‐Willemsen, Laura
Zhang, Ya‐nan
Ibrahim, Irwani
Ooi, Shirley B.S.
Wang, Jiong‐Wei
Mazlan, Muhammad I.
Kuan, Win S.
Chan, Siew‐Pang
Peelen, Linda M.
Grobbee, Diederick E.
Richards, A. Mark
Lam, Carolyn S.P.
de Kleijn, Dominique P.V.
author_sort Verbree‐Willemsen, Laura
collection PubMed
description AIMS: Extracellular vesicles (EVs) are small double‐membrane plasma vesicles that play key roles in cellular crosstalk and mechanisms such as inflammation. The role of EVs in combined organ failure such as cardiorenal syndrome has not been investigated. The aim of this study is to identify EV proteins that are associated with renal dysfunction, heart failure, and their combination in dyspnoeic patients. METHODS AND RESULTS: Blood samples were prospectively collected in 404 patients presenting with breathlessness at the emergency department at National University Hospital, Singapore. Renal dysfunction was defined as estimated glomerular filtration rate < 60 mL/min/1.73 m(2). The presence of heart failure was independently adjudicated by two clinicians on the basis of the criteria of the European Society of Cardiology guidelines. Protein levels of SerpinG1, SerpinF2, Cystatin C, and CD14 were measured with a quantitative immune assay within three EV sub‐fractions and in plasma and were tested for their associations with renal dysfunction, heart failure, and the concurrence of both conditions using multinomial regression analysis, thereby correcting for confounders such as age, gender, ethnicity, and co‐morbidities. Renal dysfunction was found in 92 patients (23%), while heart failure was present in 141 (35%). In total, 58 patients (14%) were diagnosed with both renal dysfunction and heart failure. Regression analysis showed that Cystatin C was associated with renal dysfunction, heart failure, and their combination in all three EV sub‐fractions and in plasma. CD14 was associated with both renal dysfunction and the combined renal dysfunction and heart failure in all EV sub‐fractions, and with presence of heart failure in the high density lipoprotein sub‐fraction. SerpinG1 and SerpinF2 were associated with heart failure in, respectively, two and one out of three EV sub‐fractions and in plasma, but not with renal dysfunction. CONCLUSIONS: We provide the first data showing that Cystatin C and CD14 in circulating EVs are associated with both renal dysfunction and heart failure in patients presenting with acute dyspnoea. This suggests that EV proteins may be involved in the combined organ failure of the cardiorenal syndrome and may represent possible targets for prevention or treatment.
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spelling pubmed-75242272020-10-02 Extracellular vesicle Cystatin C and CD14 are associated with both renal dysfunction and heart failure Verbree‐Willemsen, Laura Zhang, Ya‐nan Ibrahim, Irwani Ooi, Shirley B.S. Wang, Jiong‐Wei Mazlan, Muhammad I. Kuan, Win S. Chan, Siew‐Pang Peelen, Linda M. Grobbee, Diederick E. Richards, A. Mark Lam, Carolyn S.P. de Kleijn, Dominique P.V. ESC Heart Fail Original Research Articles AIMS: Extracellular vesicles (EVs) are small double‐membrane plasma vesicles that play key roles in cellular crosstalk and mechanisms such as inflammation. The role of EVs in combined organ failure such as cardiorenal syndrome has not been investigated. The aim of this study is to identify EV proteins that are associated with renal dysfunction, heart failure, and their combination in dyspnoeic patients. METHODS AND RESULTS: Blood samples were prospectively collected in 404 patients presenting with breathlessness at the emergency department at National University Hospital, Singapore. Renal dysfunction was defined as estimated glomerular filtration rate < 60 mL/min/1.73 m(2). The presence of heart failure was independently adjudicated by two clinicians on the basis of the criteria of the European Society of Cardiology guidelines. Protein levels of SerpinG1, SerpinF2, Cystatin C, and CD14 were measured with a quantitative immune assay within three EV sub‐fractions and in plasma and were tested for their associations with renal dysfunction, heart failure, and the concurrence of both conditions using multinomial regression analysis, thereby correcting for confounders such as age, gender, ethnicity, and co‐morbidities. Renal dysfunction was found in 92 patients (23%), while heart failure was present in 141 (35%). In total, 58 patients (14%) were diagnosed with both renal dysfunction and heart failure. Regression analysis showed that Cystatin C was associated with renal dysfunction, heart failure, and their combination in all three EV sub‐fractions and in plasma. CD14 was associated with both renal dysfunction and the combined renal dysfunction and heart failure in all EV sub‐fractions, and with presence of heart failure in the high density lipoprotein sub‐fraction. SerpinG1 and SerpinF2 were associated with heart failure in, respectively, two and one out of three EV sub‐fractions and in plasma, but not with renal dysfunction. CONCLUSIONS: We provide the first data showing that Cystatin C and CD14 in circulating EVs are associated with both renal dysfunction and heart failure in patients presenting with acute dyspnoea. This suggests that EV proteins may be involved in the combined organ failure of the cardiorenal syndrome and may represent possible targets for prevention or treatment. John Wiley and Sons Inc. 2020-07-10 /pmc/articles/PMC7524227/ /pubmed/32648717 http://dx.doi.org/10.1002/ehf2.12699 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Articles
Verbree‐Willemsen, Laura
Zhang, Ya‐nan
Ibrahim, Irwani
Ooi, Shirley B.S.
Wang, Jiong‐Wei
Mazlan, Muhammad I.
Kuan, Win S.
Chan, Siew‐Pang
Peelen, Linda M.
Grobbee, Diederick E.
Richards, A. Mark
Lam, Carolyn S.P.
de Kleijn, Dominique P.V.
Extracellular vesicle Cystatin C and CD14 are associated with both renal dysfunction and heart failure
title Extracellular vesicle Cystatin C and CD14 are associated with both renal dysfunction and heart failure
title_full Extracellular vesicle Cystatin C and CD14 are associated with both renal dysfunction and heart failure
title_fullStr Extracellular vesicle Cystatin C and CD14 are associated with both renal dysfunction and heart failure
title_full_unstemmed Extracellular vesicle Cystatin C and CD14 are associated with both renal dysfunction and heart failure
title_short Extracellular vesicle Cystatin C and CD14 are associated with both renal dysfunction and heart failure
title_sort extracellular vesicle cystatin c and cd14 are associated with both renal dysfunction and heart failure
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524227/
https://www.ncbi.nlm.nih.gov/pubmed/32648717
http://dx.doi.org/10.1002/ehf2.12699
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