It has been previously demonstrated that hyperglycaemia activates haem
ostasis; diabetes mellitus is considered a thrombosis-prone state. Aca
rbose, by inhibiting dietary carbohydrate absorption, reduces post-mea
l hyperglycaemia. In this study we. evaluated the effect of post-meal
hyperglycaemia on two markers of coagulation activation: prothrombin f
ragments 1+2 and D-dimer. Seventeen non-insulin-dependent diabetic pat
ients maintained on diet therapy alone were randomly assigned to recei
ve - with a cross-over study design - acarbose (100 mg orally) or plac
ebo before a standard meal. Blood samples for measurement of plasma gl
ucose, insulin, prothrombin fragments 1+2 and D-dimer were drawn at 0,
60, 120 and 240 min. After both placebo and acarbose, hyperglycaemia
and hyperinsulinaemia which followed a standard meal were accompanied
by a significant increase of plasma concentration of prothrombin fragm
ents 1+2 and D-dimer in comparison to their baseline values. Acarbose
administration significantly reduced the rise of glucose, insulin, pro
thrombin fragments 1+2 and D-dimer from 0 to 240 min in comparison to
placebo. We conclude that post-meal hyperglycaemia, at the level reach
ed by many diabetic patients on diet therapy alone, induces a coagulat
ion activation, Acarbose, by decreasing post-meal hyperglycaemia, may
be useful in reducing meal-induced activation of haemostasis in diabet
ic patients.