G. Jorneskog et al., Fibrin gel structure in diabetic patients before and during treatment withacetylsalicylic acid: a pilot study, FIBRINOL PR, 12(6), 1998, pp. 360-365
Objective: To investigate if treatment with a low daily dose of acetylsalic
ylic acid (ASA) may increase fibrin gel porosity in patients with diabetes
mellitus. Design: A pilot-study. Setting.: Out-patient clinic, Department o
f Endocrinology and Diabetology, Karolinska Hospital, Stockholm. Patients:
10 patients with type 1 diabetes. Interventions: Treatment with 75 mg ASA (
Trombyl, Pharmacia & Upjohn, Uppsala, Sweden) once daily far 5 weeks, Venou
s blood samples were drawn before and at the end of the treatment period fo
r determination of metabolic control, plasma fibrinogen level, and plasma f
ibrin gel structure. Main outcome measures: The long-term metabolic status
was determined by fructosamine and glycosylated hemoglobin (HbA1c) in blood
. The properties of the plasma fibrin gel structure, i.e. the permeability
coefficient (Ks) and the fibre mass-length ratio (mu) formed in recalcified
plasma on addition of thrombin were investigated. Results: The mean values
of HbA1c and fructosamine were not significantly changed during, as compar
ed to before, treatment with ASA. Plasma fibrinogen increased slightly (p =
0.05), while fibrin gel porosity, as assessed by Ks and mu, increased sign
ificantly (p < 0.05) in eight of the patients during treatment with ASA. Th
e increase was most pronounced in three patients who at the same time impro
ved HbA1c more than 10%. In contrast, Ks and mu decreased in two patients w
ho experienced complications during the treatment. Conclusion: The results
of this pilot study indicate that ASA may have positive effects on the fibr
in gel porosity in patients with type I diabetes. However, long-term metabo
lic control seems also important, while the positive effects on fibrin gel
structure seem abolished when inflammatory processes are present. Further s
tudies are strongly needed to investigate factors influencing plasma fibrin
ogen and fibrin gel structure.