Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/6371
Title: Platelet, monocyte and neutrophil activation and glucose tolerance in South African Mixed Ancestry individuals
Authors: Davison, Glenda Mary 
Nkambule, Bongani B 
Mkandla, Zibusiso 
Hon, Gloudina M 
Kengne, Andre Pascal 
Erasmus, Rajiv T 
Matsha, Tandi 
Keywords: Platelet activation;Type 2 diabetes mellitus;South African Mixed Ancestry individuals
Issue Date: 2017
Publisher: Scientific Reports
Journal: Scientific Reports 
Abstract: 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.
URI: http://dx.doi.org/10.1038/srep40329
http://hdl.handle.net/11189/6371
ISSN: 2045-2322
Appears in Collections:HWSci - Journal Articles (DHET subsidised)

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