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Haemodiafiltration elicits less platelet activation compared to haemodialysis

BACKGROUND: Mortality in patients with end-stage renal disorders is often a consequence of cardiovascular complications. Renal replacement therapies may contribute to this morbidity by promoting cellular activation. In renal failure patients peripheral blood samples were investigated for platelet an...

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Autores principales: Becs, Gergely, Hudák, Renáta, Fejes, Zsolt, Debreceni, Ildikó Beke, Bhattoa, Harjit Pal, Balla, József, Kappelmayer, János
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064778/
https://www.ncbi.nlm.nih.gov/pubmed/27737645
http://dx.doi.org/10.1186/s12882-016-0364-x
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author Becs, Gergely
Hudák, Renáta
Fejes, Zsolt
Debreceni, Ildikó Beke
Bhattoa, Harjit Pal
Balla, József
Kappelmayer, János
author_facet Becs, Gergely
Hudák, Renáta
Fejes, Zsolt
Debreceni, Ildikó Beke
Bhattoa, Harjit Pal
Balla, József
Kappelmayer, János
author_sort Becs, Gergely
collection PubMed
description BACKGROUND: Mortality in patients with end-stage renal disorders is often a consequence of cardiovascular complications. Renal replacement therapies may contribute to this morbidity by promoting cellular activation. In renal failure patients peripheral blood samples were investigated for platelet and endothelial cell activation markers to compare the effects of haemodiafiltration (HDF) and haemodialysis (HD). METHODS: Overall 28 patients were included in the study. Platelet P-selectin and leukocyte - platelet heterotypic aggregates were studied by flow cytometry. Soluble P- and E-selectin values were determined by ELISA, while von Willebrand factor (vWF) antigen levels were measured by immunoturbidimetry. Statistical analysis was done by the SPSS v22 software. RESULTS: Platelet surface P-selectin was below 3.0 % in healthy controls, but it was higher during the dialysis after 4 h, 8 % and 14.3 % in HDF and HD, respectively. Monocyte-platelet heterotypic aggregates were significantly elevated after 4 h in both treatments, up to 69.2 % in HDF and to 82.9 % in HD. Soluble P-selectin levels were also significantly elevated by the end of both treatment procedures (p < 0.001), vWF antigen values, however, showed elevation only during HD treatment. CONCLUSIONS: The attenuated platelet activating effects of HDF compared to HD may contribute to a less unfavourable vascular effect in this treatment modality. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12882-016-0364-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-50647782016-10-18 Haemodiafiltration elicits less platelet activation compared to haemodialysis Becs, Gergely Hudák, Renáta Fejes, Zsolt Debreceni, Ildikó Beke Bhattoa, Harjit Pal Balla, József Kappelmayer, János BMC Nephrol Research Article BACKGROUND: Mortality in patients with end-stage renal disorders is often a consequence of cardiovascular complications. Renal replacement therapies may contribute to this morbidity by promoting cellular activation. In renal failure patients peripheral blood samples were investigated for platelet and endothelial cell activation markers to compare the effects of haemodiafiltration (HDF) and haemodialysis (HD). METHODS: Overall 28 patients were included in the study. Platelet P-selectin and leukocyte - platelet heterotypic aggregates were studied by flow cytometry. Soluble P- and E-selectin values were determined by ELISA, while von Willebrand factor (vWF) antigen levels were measured by immunoturbidimetry. Statistical analysis was done by the SPSS v22 software. RESULTS: Platelet surface P-selectin was below 3.0 % in healthy controls, but it was higher during the dialysis after 4 h, 8 % and 14.3 % in HDF and HD, respectively. Monocyte-platelet heterotypic aggregates were significantly elevated after 4 h in both treatments, up to 69.2 % in HDF and to 82.9 % in HD. Soluble P-selectin levels were also significantly elevated by the end of both treatment procedures (p < 0.001), vWF antigen values, however, showed elevation only during HD treatment. CONCLUSIONS: The attenuated platelet activating effects of HDF compared to HD may contribute to a less unfavourable vascular effect in this treatment modality. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12882-016-0364-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-13 /pmc/articles/PMC5064778/ /pubmed/27737645 http://dx.doi.org/10.1186/s12882-016-0364-x Text en © The Author(s). 2016 Open AccessThis 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
Becs, Gergely
Hudák, Renáta
Fejes, Zsolt
Debreceni, Ildikó Beke
Bhattoa, Harjit Pal
Balla, József
Kappelmayer, János
Haemodiafiltration elicits less platelet activation compared to haemodialysis
title Haemodiafiltration elicits less platelet activation compared to haemodialysis
title_full Haemodiafiltration elicits less platelet activation compared to haemodialysis
title_fullStr Haemodiafiltration elicits less platelet activation compared to haemodialysis
title_full_unstemmed Haemodiafiltration elicits less platelet activation compared to haemodialysis
title_short Haemodiafiltration elicits less platelet activation compared to haemodialysis
title_sort haemodiafiltration elicits less platelet activation compared to haemodialysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064778/
https://www.ncbi.nlm.nih.gov/pubmed/27737645
http://dx.doi.org/10.1186/s12882-016-0364-x
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