COLLAGEN-SYNTHESIS MARKERS AND MATRIX METALLOPROTEINASES-2 (MMP-2) AND METALLOPROTEINASES-9 (MMP-9) IN THE SUCTION BLISTER FLUID AND SERUM OF JUVENILE DIABETIC-PATIENTS
Ap. Annala et al., COLLAGEN-SYNTHESIS MARKERS AND MATRIX METALLOPROTEINASES-2 (MMP-2) AND METALLOPROTEINASES-9 (MMP-9) IN THE SUCTION BLISTER FLUID AND SERUM OF JUVENILE DIABETIC-PATIENTS, EJD. European journal of dermatology, 5(3), 1995, pp. 247-252
In diabetes, various connective tissue alterations have been noted in
the skin, such as thickening of the dermis and changes in the basement
membranes. The mechanisms behind these changes are not known. In the
present study, skin thickness and markers of collagen synthesis and de
gradation were studied in 17 male, juvenile diabetic patients and in 1
1 healthy, male controls. As markers of collagen synthesis, C-propepti
des and N-propeptides of type I procollagen (PICP and PINP) and N-prop
eptides of type III procollagen (PIIINP) were measured both from sucti
on blister fluid and serum. As markers of collagen degradation, the ma
trix metalloproteinases MMP-2 (72 kDa gelatinase) and MMP-9 (92 kDa ge
latinase) were assayed by the zymography method from the blister fluid
s and serum. No marked changes could be found in the skin thickness of
the diabetic patients compared to the controls when the A-scan ultras
ound technique was used. In general the concentrations of the collagen
propeptides and the matrix metalloproteinases were remarkably similar
In the diabetic patients and the controls in both the suction blister
Fluid and the serum. Interestingly, the concentrations of PINP in the
blister fluid in the diabetic patients with long established disease
were lower than those in the controls and the PICP/PINP ratio was ther
efore significantly higher (p < 0.05) in these patients than in the co
ntrols. This may be due to either a rate of PINP into the blister cavi
ty. Since the ratio of PICP/PINP was not changed to the same extent in
the serum as in the blister fluid, there is probably no generalized c
leavage defect of procollagens present in diabetes.