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Platelet, monocyte and neutrophil activation and glucose tolerance in South African Mixed Ancestry individuals

Platelet activation has been described in patients with chronic inflammation, however in type 2 diabetes mellitus it remains controversial. We compared levels of platelet leucocyte aggregates, monocyte and granulocyte activation across glucose tolerance statuses in mixed ancestry South Africans. Ind...

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Autores principales: Davison, Glenda M., Nkambule, Bongani B., Mkandla, Zibusiso, Hon, Gloudina M., Kengne, Andre P., Erasmus, Rajiv T., Matsha, Tandi E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238515/
https://www.ncbi.nlm.nih.gov/pubmed/28091589
http://dx.doi.org/10.1038/srep40329
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author Davison, Glenda M.
Nkambule, Bongani B.
Mkandla, Zibusiso
Hon, Gloudina M.
Kengne, Andre P.
Erasmus, Rajiv T.
Matsha, Tandi E.
author_facet Davison, Glenda M.
Nkambule, Bongani B.
Mkandla, Zibusiso
Hon, Gloudina M.
Kengne, Andre P.
Erasmus, Rajiv T.
Matsha, Tandi E.
author_sort Davison, Glenda M.
collection PubMed
description Platelet activation has been described in patients with chronic inflammation, however in type 2 diabetes mellitus it remains controversial. We compared levels of platelet leucocyte aggregates, monocyte and granulocyte activation across glucose tolerance statuses in mixed ancestry South Africans. Individuals (206) were recruited from Bellville-South, Cape Town, and included 66% with normal glucose tolerance, 18.7% pre-diabetes, 8.7% screen-detected diabetes and 6.3% known diabetes. Monocyte and neutrophil activation were measured by calculating the percentage of cells expressing CD142 and CD69 while platelet monocyte aggregates were defined as CD14(++) CD42b(+) events and platelet neutrophil aggregates as CD16(++) CD42b(+) events. The percentage of monocytes and neutrophils expressing CD69 and CD142 was significantly higher in known diabetes and prediabetes, but, lowest in screen-detected diabetes (both p ≤ 0.016). The pattern was similar for platelet monocyte and neutrophil aggregates (both p ≤ 0.003). In robust linear regressions adjusted for age and gender, known diabetes was significantly and positively associated with the percentage of monocytes expressing CD69 [beta 11.06 (p = 0.016)] and CD42b (PMAs) [19.51 (0.003)] as well as the percentage of neutrophils expressing CD69 [14.19 (<0.0001)] and CD42b [17.7 (0.001)]. We conclude that monitoring platelet activation in diagnosed diabetic patients may have a role in the management and risk stratification.
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spelling pubmed-52385152017-01-19 Platelet, monocyte and neutrophil activation and glucose tolerance in South African Mixed Ancestry individuals Davison, Glenda M. Nkambule, Bongani B. Mkandla, Zibusiso Hon, Gloudina M. Kengne, Andre P. Erasmus, Rajiv T. Matsha, Tandi E. Sci Rep Article Platelet activation has been described in patients with chronic inflammation, however in type 2 diabetes mellitus it remains controversial. We compared levels of platelet leucocyte aggregates, monocyte and granulocyte activation across glucose tolerance statuses in mixed ancestry South Africans. Individuals (206) were recruited from Bellville-South, Cape Town, and included 66% with normal glucose tolerance, 18.7% pre-diabetes, 8.7% screen-detected diabetes and 6.3% known diabetes. Monocyte and neutrophil activation were measured by calculating the percentage of cells expressing CD142 and CD69 while platelet monocyte aggregates were defined as CD14(++) CD42b(+) events and platelet neutrophil aggregates as CD16(++) CD42b(+) events. The percentage of monocytes and neutrophils expressing CD69 and CD142 was significantly higher in known diabetes and prediabetes, but, lowest in screen-detected diabetes (both p ≤ 0.016). The pattern was similar for platelet monocyte and neutrophil aggregates (both p ≤ 0.003). In robust linear regressions adjusted for age and gender, known diabetes was significantly and positively associated with the percentage of monocytes expressing CD69 [beta 11.06 (p = 0.016)] and CD42b (PMAs) [19.51 (0.003)] as well as the percentage of neutrophils expressing CD69 [14.19 (<0.0001)] and CD42b [17.7 (0.001)]. We conclude that monitoring platelet activation in diagnosed diabetic patients may have a role in the management and risk stratification. Nature Publishing Group 2017-01-16 /pmc/articles/PMC5238515/ /pubmed/28091589 http://dx.doi.org/10.1038/srep40329 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Davison, Glenda M.
Nkambule, Bongani B.
Mkandla, Zibusiso
Hon, Gloudina M.
Kengne, Andre P.
Erasmus, Rajiv T.
Matsha, Tandi E.
Platelet, monocyte and neutrophil activation and glucose tolerance in South African Mixed Ancestry individuals
title Platelet, monocyte and neutrophil activation and glucose tolerance in South African Mixed Ancestry individuals
title_full Platelet, monocyte and neutrophil activation and glucose tolerance in South African Mixed Ancestry individuals
title_fullStr Platelet, monocyte and neutrophil activation and glucose tolerance in South African Mixed Ancestry individuals
title_full_unstemmed Platelet, monocyte and neutrophil activation and glucose tolerance in South African Mixed Ancestry individuals
title_short Platelet, monocyte and neutrophil activation and glucose tolerance in South African Mixed Ancestry individuals
title_sort platelet, monocyte and neutrophil activation and glucose tolerance in south african mixed ancestry individuals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238515/
https://www.ncbi.nlm.nih.gov/pubmed/28091589
http://dx.doi.org/10.1038/srep40329
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