Dm. Heywood et al., LEVELS OF VON-WILLEBRAND-FACTOR, INSULIN-RESISTANCE SYNDROME AND A COMMON VWF GENE POLYMORPHISM IN NONINSULIN-DEPENDENT (TYPE-2) DIABETES-MELLITUS, Diabetic medicine, 13(8), 1996, pp. 720-725
Citations number
30
Categorie Soggetti
Endocrynology & Metabolism","Medicine, General & Internal
To examine the association between von Willebrand Factor (VWF) concent
rations and features of the insulin resistance syndrome, 208 patients
with Type 2 (non-insulin-dependent) diabetes (NIDDM) and 80 healthy co
ntrols were studied. A restriction fragment length polymorphism in exo
n 12 of the VWF gene, detected by Aat II endonuclease, was also examin
ed. vWF concentrations were elevated in the patient group (patients 1.
28 IU ml(-1) vs controls 1.12 IU ml(-1), p = 0.003). Genotype frequenc
ies were in Hardy-Weinberg equilibrium and genotype did not relate to
vWF levels: means (95 % Cl) were AA 1.29 (1.29-1.44) IU ml(-1) n = 155
. vWF correlated with (r = 0.23, p < 0.001), and fibrinogen (r = 0.22,
p = 0.002) in the patient group, but was unrelated to blood lipids, H
bA(1C), body mass index, glucose, hypertension and smoking. In a linea
r regression model, age and insulin remained as independent predictors
of VWF levels, explaining 16 % of inter-individual variance in the pa
tient group. In conclusion, these findings show VWF concentrations are
elevated in NIDDM and are weakly related to features of the insulin r
esistance syndrome. No relationship was demonstrated between the gene
polymorphism studied and vWF concentrations in this group.