TY - JOUR
T1 - High-risk type-2 diabetes mellitus patients, without prior ischemic events, have normal blood platelet functionality profiles
T2 - A cross-sectional study
AU - Shlomai, Gadi
AU - Haran-Appel, Tal
AU - Sella, Tal
AU - Grossman, Yoni
AU - Hauschner, Hagit
AU - Rosenberg, Nurit
AU - Ehud, Grossman
N1 - Publisher Copyright:
© Shlomai et al.
PY - 2015/6/12
Y1 - 2015/6/12
N2 - Background: Patients with type 2 diabetes mellitus (DM) display a predisposition for vascular disease. Platelets taken from vasculopathic diabetic patients, show enhanced stimuli-induced activation and aggregation responses. Aspirin remains the cornerstone antiplatelet agent for secondary prevention of vascular complications among diabetic patients, yet evidence of its efficacy and safety in primary prevention are conflicting. Our aim was to assess whether high risk diabetic patients, without previous ischemic events, have abnormal platelet functionality profiles. Methods: The study included 82 diabetic patients and 86 matched non-diabetic patients without prior ischemic events nor treatment with anti-platelet medications. Blood samples were analyzed for platelet markers of activation, turnover and leukocyte-platelet interactions. Results: Our final analysis included 122 males (74 %), with a mean age of 61 years. Mean platelet volume (MPV) was similar between the diabetic patients and controls (9.2 fL for both). Following activation, PAC-1 binding and P-selectin expression were found comparable between the diabetic patients and controls (83 % versus 81 % and 76 % versus 74 %, respectively). Leukocyte-platelet aggregates (LPAs) were similar between the diabetic patients and controls (18 % versus 17 %, respectively). Neutrophil-platelet aggregates (NPAs) and monocyte-platelet aggregates (MPAs) were also found similar in the diabetic patients and controls. Elevated fasting plasma glucose was associated with increased LPAs rates. Conclusions: High risk type-2 diabetes mellitus patients, without prior ischemic events, have normal blood platelet functionality profiles.
AB - Background: Patients with type 2 diabetes mellitus (DM) display a predisposition for vascular disease. Platelets taken from vasculopathic diabetic patients, show enhanced stimuli-induced activation and aggregation responses. Aspirin remains the cornerstone antiplatelet agent for secondary prevention of vascular complications among diabetic patients, yet evidence of its efficacy and safety in primary prevention are conflicting. Our aim was to assess whether high risk diabetic patients, without previous ischemic events, have abnormal platelet functionality profiles. Methods: The study included 82 diabetic patients and 86 matched non-diabetic patients without prior ischemic events nor treatment with anti-platelet medications. Blood samples were analyzed for platelet markers of activation, turnover and leukocyte-platelet interactions. Results: Our final analysis included 122 males (74 %), with a mean age of 61 years. Mean platelet volume (MPV) was similar between the diabetic patients and controls (9.2 fL for both). Following activation, PAC-1 binding and P-selectin expression were found comparable between the diabetic patients and controls (83 % versus 81 % and 76 % versus 74 %, respectively). Leukocyte-platelet aggregates (LPAs) were similar between the diabetic patients and controls (18 % versus 17 %, respectively). Neutrophil-platelet aggregates (NPAs) and monocyte-platelet aggregates (MPAs) were also found similar in the diabetic patients and controls. Elevated fasting plasma glucose was associated with increased LPAs rates. Conclusions: High risk type-2 diabetes mellitus patients, without prior ischemic events, have normal blood platelet functionality profiles.
KW - Aspirin
KW - Cardiovascular risk
KW - Diabetes mellitus
KW - Platelets activity
KW - Primary prevention
UR - http://www.scopus.com/inward/record.url?scp=84931270915&partnerID=8YFLogxK
U2 - 10.1186/s12933-015-0244-x
DO - 10.1186/s12933-015-0244-x
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AN - SCOPUS:84931270915
SN - 1475-2840
VL - 14
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
IS - 1
M1 - 80
ER -