We measured levels of platelet-derived microparticles (PMP), which have coa
gulative activity and are produced by platelet activation or physical stimu
lation, and CD62P/ CD63-positive platelets in patients with diabetes mellit
us to determine their clinical significance and effects on complications of
diabetes including diabetic nephropathy. We also compared these levels bef
ore and after administration of the antiplatelet drug cilostazol. Plasma PM
P and CD62P/CD63-positive platelet levels were significantly higher in pati
ents with diabetes mellitus than normal controls. CD62P-positive platelet l
evels were significantly higher in patients with nephropathy than in patien
ts without complications. After administration of cilostazol, PMP and CD62P
/CD63-positive platelet levels were significantly decreased. The increases
in platelet activity and its related procoagulant activity appear to accoun
t in part for the hypercoagulability observed in diabetes mellitus. Our fin
dings suggest that activated platelets might play a role in the development
of diabetic nephropathy. Furthermore, antiplatelet therapy with cilostazol
for diabetic patients may be useful as antithrombin therapy including anti
platelet therapy, since it suppresses the production of intrinsic coagulant
s produced by platelet activation.