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Published on: April 1, 2015
Diabetic ketoacidosis promotes a prothrombotic state
G F Carl1, William H Hoffman, Gregory G Passmore
1Department of Neurology, Veteran's Administration Medical Center, Augusta, Georgia, USA.
Insights
Diabetic ketoacidosis (DKA) in children creates a prothrombotic state, increasing stroke risk. Treatment slowly normalizes clotting factors, but elevated von Willebrand factor persists, indicating ongoing vascular activation.
Area of Science:
- Pediatric Endocrinology
- Hematology
- Vascular Biology
Background:
- Cerebrovascular accidents (CVAs) are severe complications in pediatric diabetic ketoacidosis (DKA).
- Understanding DKA's impact on thrombotic factors is crucial for CVA prevention.
Purpose of the Study:
- To investigate the effects of DKA and its treatment on key hemostatic and thrombotic factors in adolescents.
- To evaluate changes in protein C, protein S, von Willebrand factor (vWF), fibrinogen, homocysteine, and folate.
Main Methods:
- Prospective study of seven adolescents with DKA.
- Measurement of thrombotic factors before and at 6, 24, and 120 hours after DKA treatment initiation.
Main Results:
- DKA decreased protein C activity and free protein S levels.
- Von Willebrand factor (vWF) antigen and activity were elevated pre-treatment and vWF activity remained high post-treatment.
- Homocysteine decreased pre-treatment, while folate increased, with reciprocal changes during treatment.
Conclusions:
- DKA and its treatment induce a prothrombotic state characterized by reduced protein C and free protein S, and increased vWF.
- Endothelial activation during DKA contributes to the risk of cerebrovascular accidents in children and adolescents.
Abstract:
Cerebrovascular accidents are one of the life-threatening complications of diabetic ketoacidosis (DKA) in children and adolescents. Our objective was to evaluate the effect of DKA and its treatment on factors known to affect thrombotic activity (protein C; protein S; von Willebrand factor, fibrinogen; homocysteine; and folate) by comparing seven adolescents with DKA prior to treatment and at 6, 24, and 120 hours after initiation of treatment. We found that protein C activity was significantly decreased by DKA, but normalized slowly following treatment. Free protein S was low throughout the study. Protein C antigen and protein S antigen showed varying degrees ofchange within the first 24 hours, but remained in the normal range, with the exception of the initial value of protein C antigen, which was elevated. von Willebrand factor (vWF) antigen and vWF activity were both significantly increased prior to treatment, but decreased with treatment. However, vWF activity remained elevated at 120 hours. Fibrinogen concentrations showed no significant changes throughout the study. Homocysteine was significantly decreased prior to treatment and increased with the initiation of treatment Folate was significantly increased prior to treatment, and decreased to high normal levels. The increased vWF and the decreased levels of protein C activity and of free protein S support the hypothesis that DKA and its treatment results in a prothrombotic state and activation of the vascular endothelium, which, in turn, predispose to cerebrovascular accidents.
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