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Updated: May 26, 2026

Experimental and Imaging Techniques for Examining Fibrin Clot Structures in Normal and Diseased States
Published on: April 1, 2015
High-dose aspirin is required to influence plasma fibrin network structure in patients with type 1 diabetes
Sara Tehrani1, Aleksandra Antovic, Fariborz Mobarrez
1Division of Medicine, Department of Clinical Sciences, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden. sara.tehrani@ds.se
Insights
High-dose aspirin (320 mg) improved fibrin network permeability in type 1 diabetes patients, unlike low-dose aspirin. This suggests higher aspirin doses may be needed to effectively manage cardiovascular disease risk in this population.
Area of Science:
- Cardiovascular Disease Research
- Diabetes Mellitus Therapeutics
- Hematology and Thrombosis
Background:
- Type 1 diabetes is associated with a less permeable fibrin network, increasing cardiovascular disease (CVD) risk.
- Standard low-dose aspirin treatment for CVD may be less effective in diabetic patients.
- Aspirin's impact on fibrin network permeability and its interaction with glycemic control in type 1 diabetes requires investigation.
Purpose of the Study:
- To investigate the effects of low- and high-dose aspirin on fibrin network formation in type 1 diabetes patients.
- To explore the interaction between aspirin dosage, fibrin network permeability, and glycemic control in type 1 diabetes.
Main Methods:
- Forty-eight type 1 diabetes patients (24 good, 24 poor glycemic control) were randomized to 75 mg or 320 mg aspirin daily for 4 weeks in a crossover design.
- A 4-week washout period was implemented between treatments.
- Plasma fibrin network permeability was assessed using the permeability coefficient (K(s)).
Main Results:
- 75 mg aspirin did not affect fibrin network permeability (K(s)).
- 320 mg aspirin significantly increased K(s) (P = 0.004) compared to 75 mg (P = 0.009).
- The increase in K(s) with high-dose aspirin was significant in patients with poor glycemic control (P = 0.02) and trended in those with good control (P = 0.06).
Conclusions:
- A high aspirin dose (320 mg) is necessary to alter fibrin network permeability in type 1 diabetes.
- Low-dose aspirin's lack of effect on fibrin permeability may explain treatment failure in diabetes.
- Findings highlight the importance of aspirin dosage in managing CVD risk in type 1 diabetes.
Objective:
Patients with type 1 diabetes form a less permeable fibrin network, which could contribute to their increased risk of cardiovascular disease (CVD). Low-dose aspirin treatment is the standard in the management of CVD; however, the effect seems reduced in patients with diabetes. We investigated the effects of low- and high-dose aspirin treatment on fibrin network formation in patients with type 1 diabetes (primary aim) and the possible interaction between the treatment effects of aspirin on fibrin network permeability and glycemic control in these patients (secondary aim).
Research Design And Methods:
Forty-eight patients (24 subjects with good [HbA(1c) <7.4%] and 24 subjects with poor [HbA(1c) >8.4%] glycemic control) were randomly assigned to treatment with 75 or 320 mg/day aspirin during 4 weeks in a crossover fashion. A 4-week washout period separated the treatment periods. The plasma fibrin network was assessed by determination of the permeability coefficient (K(s)).
Results:
Treatment with 75 mg aspirin did not influence fibrin network permeability (K(s)). However, K(s) increased significantly during treatment with 320 mg aspirin (P = 0.004), and a significant treatment effect was seen compared with treatment with 75 mg aspirin (P = 0.009). The increase in K(s) during high-dose aspirin treatment was significant in patients with poor glycemic control (P = 0.02), whereas K(s) only tended to increase in patients with good glycemic control (P = 0.06).
Conclusions:
A high dose of aspirin is required to influence fibrin network permeability in patients with type 1 diabetes. The observed lack of effect with low-dose aspirin may contribute to aspirin treatment failure in diabetes.
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