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Platelet adhesion in type 2 diabetes: impact of plasma albumin and mean platelet volume

BACKGROUND: Altered mean platelet volume (MPV) and plasma albumin has been reported in type 2 diabetes (T2D). MPV is suggested to predict cardiovascular risk but there is a lack of evidence for associations between MPV and platelet adhesion. Plasma albumin and magnesium are other factors reported to...

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Autores principales: Johansson, Mona, Eriksson, Andreas C., Östgren, Carl Johan, Whiss, Per A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173756/
https://www.ncbi.nlm.nih.gov/pubmed/34078390
http://dx.doi.org/10.1186/s12959-021-00291-w
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author Johansson, Mona
Eriksson, Andreas C.
Östgren, Carl Johan
Whiss, Per A.
author_facet Johansson, Mona
Eriksson, Andreas C.
Östgren, Carl Johan
Whiss, Per A.
author_sort Johansson, Mona
collection PubMed
description BACKGROUND: Altered mean platelet volume (MPV) and plasma albumin has been reported in type 2 diabetes (T2D). MPV is suggested to predict cardiovascular risk but there is a lack of evidence for associations between MPV and platelet adhesion. Plasma albumin and magnesium are other factors reported to influence thrombotic risk. The objectives of this study were to assess the association between platelet adhesion and plasma factors with a potential role to affect platelet activation. METHODS: Blood was collected from 60 T2D patients and 60 healthy controls. Platelet adhesion to different protein surfaces induced by various soluble activators were measured in microplates. MPV, albumin and magnesium were analysed together with additional routine tests. RESULTS: Despite normal levels, plasma albumin significantly correlated with adhesion of T2D platelets but not with controls. There was a significant association between MPV and platelet adhesion in both groups, but association was smaller in T2D. Levels of glucose, HbA1c or magnesium did not correlate with platelet adhesion. CONCLUSIONS: Plasma albumin was associated with platelet adhesion in T2D suggesting that albumin may be a factor to consider upon cardiovascular risk assessment. MPV was more associated with the level of platelet adhesion in healthy individuals than in well-controlled T2D patients.
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spelling pubmed-81737562021-06-03 Platelet adhesion in type 2 diabetes: impact of plasma albumin and mean platelet volume Johansson, Mona Eriksson, Andreas C. Östgren, Carl Johan Whiss, Per A. Thromb J Research BACKGROUND: Altered mean platelet volume (MPV) and plasma albumin has been reported in type 2 diabetes (T2D). MPV is suggested to predict cardiovascular risk but there is a lack of evidence for associations between MPV and platelet adhesion. Plasma albumin and magnesium are other factors reported to influence thrombotic risk. The objectives of this study were to assess the association between platelet adhesion and plasma factors with a potential role to affect platelet activation. METHODS: Blood was collected from 60 T2D patients and 60 healthy controls. Platelet adhesion to different protein surfaces induced by various soluble activators were measured in microplates. MPV, albumin and magnesium were analysed together with additional routine tests. RESULTS: Despite normal levels, plasma albumin significantly correlated with adhesion of T2D platelets but not with controls. There was a significant association between MPV and platelet adhesion in both groups, but association was smaller in T2D. Levels of glucose, HbA1c or magnesium did not correlate with platelet adhesion. CONCLUSIONS: Plasma albumin was associated with platelet adhesion in T2D suggesting that albumin may be a factor to consider upon cardiovascular risk assessment. MPV was more associated with the level of platelet adhesion in healthy individuals than in well-controlled T2D patients. BioMed Central 2021-06-02 /pmc/articles/PMC8173756/ /pubmed/34078390 http://dx.doi.org/10.1186/s12959-021-00291-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Johansson, Mona
Eriksson, Andreas C.
Östgren, Carl Johan
Whiss, Per A.
Platelet adhesion in type 2 diabetes: impact of plasma albumin and mean platelet volume
title Platelet adhesion in type 2 diabetes: impact of plasma albumin and mean platelet volume
title_full Platelet adhesion in type 2 diabetes: impact of plasma albumin and mean platelet volume
title_fullStr Platelet adhesion in type 2 diabetes: impact of plasma albumin and mean platelet volume
title_full_unstemmed Platelet adhesion in type 2 diabetes: impact of plasma albumin and mean platelet volume
title_short Platelet adhesion in type 2 diabetes: impact of plasma albumin and mean platelet volume
title_sort platelet adhesion in type 2 diabetes: impact of plasma albumin and mean platelet volume
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173756/
https://www.ncbi.nlm.nih.gov/pubmed/34078390
http://dx.doi.org/10.1186/s12959-021-00291-w
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