THROMBOMODULIN AND INDUCED TISSUE FACTOR EXPRESSION ON MONOCYTES AS MARKERS OF DIABETIC MICROANGIOPATHY - A PROSPECTIVE-STUDY ON HEMOSTASISAND LIPOPROTEINS IN INSULIN-DEPENDENT DIABETES-MELLITUS
Jl. Reverter et al., THROMBOMODULIN AND INDUCED TISSUE FACTOR EXPRESSION ON MONOCYTES AS MARKERS OF DIABETIC MICROANGIOPATHY - A PROSPECTIVE-STUDY ON HEMOSTASISAND LIPOPROTEINS IN INSULIN-DEPENDENT DIABETES-MELLITUS, American journal of hematology, 56(2), 1997, pp. 93-99
Vascular complications are the main cause of morbidity in diabetes mel
litus, To evaluate lipoprotein and hemostatic parameters and their rel
ationship with clinically detectable microangiopathy, we studied 58 in
sulin-dependent diabetes mellitus patients and 60 controls matched for
age, sex, and body mass index, Thirteen patients presented clinically
detectable microangiopathy (8 retinopathy and 5 both retinopathy and
microalbuminuria), A cross-sectional study of lipid profile, coagulati
on parameters, and a flowcytometric evaluation of tissue factor expres
sion in normal monocytes induced by patient plasma were performed, Pat
ients were re-evaluated for microangiopathy in a 3-year median follow-
up, Patients showed triglyceride enrichment in low (P=0.00002) and hig
h density lipoproteins (P=0.004) and increased levels of D-dimer (P<0.
00001), prothrombin fragment 1 + 2 (P < 0.00001), and thrombin-antithr
ombin III complex (P = 0.0001), Patients with clinically detectable mi
croangiopathy had increased type 1 plasminogen activator inhibitor (P=
0.00001), thrombomodulin (P=0.02), and induced monocyte tissue factor
expression (P < 0.00001), Nine patients developed clinically detectabl
e microangiopathy in the follow-up and the only predictive variable wa
s increased induced tissue factor expression, In conclusion, in these
patients elevated thrombin and fibrin generation reflects a hypercoagu
lable state but clinically detectable microangiopathy seems related to
endothelial cell injury markers and to increased induced tissue facto
r expression on monocytes. (C) 1997 Wiley-Liss, Inc.