TY - JOUR
T1 - Shear-induced platelet adhesion and aggregation on subendothelium are increased in diabetic patients
AU - Knobler, Hilla
AU - Savion, Naphtali
AU - Shenkman, Boris
AU - Kotev-Emeth, Shlomo
AU - Varon, David
N1 - Funding Information:
This research was supported by a grant from the National Council for Research and Development, Israel and Deutsche Forschungsanstalt Luft and Raumfahrt. We thank Dr. Rima Dardik and Dr. Ilia Tamarin for their help in the analysis of platelet activity, and Ilana Gelernter for her help with the statistical analysis of the data.
PY - 1998/5/15
Y1 - 1998/5/15
N2 - Increased platelet aggregation has been suggested to play a role in the accelerated atherosclerosis of diabetics. However the physiological relevance of the aggregation tests has been questioned. The purpose of this study was to determine platelet activation in diabetic patients, using a novel device - the cone and plate(let) analyzer - to measure shear-induced platelet adhesion and aggregation on extracellular matrix (ECM). Whole blood platelet adhesion and aggregation in patients with noninsulin-dependent diabetes mellitus (n = 82) and in nondiabetic controls (n = 71) were compared. Clinical and laboratory characteristics of the diabetic patients were analyzed for possible correlation with parameters of platelet activity. Patients with diabetes had a significantly increased platelet activation compared to nondiabetic subjects, demonstrated by an increased adhesion to the ECM (surface coverage, 23% [95% confidence interval, 22-25%] vs. 19% [95% confidence interval, 18-20%], respectively) and an increased average size of the ECM- bound aggregates (54 μm2 [95% confidence interval, 51-57 μm2] vs. 47 μm2 [95% confidence interval, 43-51 μm2], respectively). Platelet adhesion in the diabetic group was found to correlate with triglyceride levels (r = 0.36) and hematocrit values (r = 0.31) and inversely with high- density lipoprotein cholesterol levels (r = 0.30). There were no correlation, however, between parameters of platelet reactivity and duration of diabetes, vascular complications and low-density lipoprotein levels. Our data demonstrate an increased platelet adhesion and aggregation in diabetic patients and suggest a modulatory role of diabetic dyslipidemia.
AB - Increased platelet aggregation has been suggested to play a role in the accelerated atherosclerosis of diabetics. However the physiological relevance of the aggregation tests has been questioned. The purpose of this study was to determine platelet activation in diabetic patients, using a novel device - the cone and plate(let) analyzer - to measure shear-induced platelet adhesion and aggregation on extracellular matrix (ECM). Whole blood platelet adhesion and aggregation in patients with noninsulin-dependent diabetes mellitus (n = 82) and in nondiabetic controls (n = 71) were compared. Clinical and laboratory characteristics of the diabetic patients were analyzed for possible correlation with parameters of platelet activity. Patients with diabetes had a significantly increased platelet activation compared to nondiabetic subjects, demonstrated by an increased adhesion to the ECM (surface coverage, 23% [95% confidence interval, 22-25%] vs. 19% [95% confidence interval, 18-20%], respectively) and an increased average size of the ECM- bound aggregates (54 μm2 [95% confidence interval, 51-57 μm2] vs. 47 μm2 [95% confidence interval, 43-51 μm2], respectively). Platelet adhesion in the diabetic group was found to correlate with triglyceride levels (r = 0.36) and hematocrit values (r = 0.31) and inversely with high- density lipoprotein cholesterol levels (r = 0.30). There were no correlation, however, between parameters of platelet reactivity and duration of diabetes, vascular complications and low-density lipoprotein levels. Our data demonstrate an increased platelet adhesion and aggregation in diabetic patients and suggest a modulatory role of diabetic dyslipidemia.
KW - Diabetes mellitus
KW - Platelet activation
KW - Platelet adhesion
KW - Platelets aggregation
UR - http://www.scopus.com/inward/record.url?scp=0032524379&partnerID=8YFLogxK
U2 - 10.1016/S0049-3848(98)00050-4
DO - 10.1016/S0049-3848(98)00050-4
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AN - SCOPUS:0032524379
SN - 0049-3848
VL - 90
SP - 181
EP - 190
JO - Thrombosis Research
JF - Thrombosis Research
IS - 4
ER -