Brief reportCoated-platelet levels in patients with Type 1 and with Type 2 diabetes mellitus
Section snippets
Methods
The study, which meets Declaration of Helsinki principles, was approved by local Ethics Committees, and each participant gave written informed consent. Microvascular complications were laser-treated retinopathy or increased albuminuria. Macrovascular disease was defined as clinically evident cardiovascular, cerebrovascular, or peripheral vascular disease. Venous blood was collected from 58 Type 1 and 90 Type 2 diabetic and 54 non-diabetic subjects. HbA1c, lipids, and renal function tests were
Clinical characteristics and coated-platelet levels
Age, diabetes duration and HbA1c of diabetic subjects were 52(12) years (mean (S.D.)), 14(12) years, and 8.2(1.8)%, respectively. Eighty percent of the Type 2 group were on oral agents, and 48% were on insulin. Of the diabetes group, 33% had microvascular complications and 45% had macrovascular disease. Twenty-five percent of the diabetic subjects and 9.3% of the controls were smokers. The control group was younger, 39(10) years, with lower HbA1c; 5.1 (0.4)%. Forty-five percent of diabetic and
Discussion
As coated-platelets may be pro-thrombotic and related to inflammation, we hypothesized that levels would be increased in diabetes or its complications and relate to vascular risk factors. In this, we believe the first study in diabetes, we demonstrated lack of significant difference in coated-platelet levels in Type 1 or Type 2 diabetic patients (not on dialysis) and healthy controls, nor were there differences in coated-platelets by age, gender, BMI, lipids, CRP, diabetes duration or
Conflict of interest statement
The authors declare that they have no conflict of interest.
Acknowledgements
Authors acknowledge study participants and the OU General Clinical Research Center staff. American Heart Association Grant-in-Aid (GLD).
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2014, Journal of Stroke and Cerebrovascular DiseasesCitation Excerpt :However, none of these differences were statistically significant (Table 1). To investigate the potential modifying and confounding effects of the recorded subject characteristics and clinical measures, differences in coated-platelet levels between subjects with and without CMBs were calculated after stratifying by smoking status, gender, race/ethnicity, age, use of medications that may influence coated-platelet levels (selective serotonin reuptake inhibitors, statins, or antiplatelets),19 history of diabetes,21 end-stage renal disease,22 or hypertension.23 With the exception of patients that reported taking statins, subjects with CMBs tended to have lower coated–platelet levels compared with those without CMBs regardless of the subgroup under consideration.
Higher levels of coated-platelets are observed in patients with subarachnoid hemorrhage but lower levels are associated with increased mortality at 30 days
2013, Journal of the Neurological SciencesCitation Excerpt :All data analyses for this paper were generated using SAS software, Version 9.2 of the SAS System for Windows (SAS Institute Inc., Cary, NC, USA). Table 1 lists demographics, current smoking, co-morbidities pertinent to coated-platelet levels (hypertension and diabetes) [17,18], use of medications that may alter coated-platelet levels, such as selective serotonin reuptake inhibitors (SSRIs), HMG-CoA reductase inhibitors (statins) or antiplatelet agents [1,26,27], and coated-platelet levels for patients and controls. Of note, although we planned to include patients with ≤ 96 h between the onset of the symptoms and enrollment, all blood samples were actually obtained within 48 h of onset.
Lower coated-platelet levels are associated with early hemorrhagic transformation in patients with non-lacunar brain infarction
2010, Journal of Thrombosis and HaemostasisLevels of procoagulant microparticles expressing phosphatidylserine contribute to bleeding phenotype in patients with inherited thrombocytopenia
2021, Blood Coagulation and Fibrinolysis
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These authors contributed equally.