P. Fioretto et al., HETEROGENEOUS NATURE OF MICROALBUMINURIA IN NIDDM - STUDIES OF ENDOTHELIAL FUNCTION AND RENAL STRUCTURE, Diabetologia, 41(2), 1998, pp. 233-236
Microalbuminuria (MA) is associated with microangiopathy (renal and re
tinal lesions) in insulin-dependent diabetic (IDDM) patients. In contr
ast MA does not reflect microvascular damage in a substantial number o
f non-insulin-dependent diabetic (NIDDM) patients. MA predicts cardiov
ascular disease in NIDDM patients with increased von Willebrand factor
(vWF) plasma levels which are hypothesized to reflect endothelial dys
function. However, it is not known whether MA is consequent to general
ised endothelial dysfunction or to renal injury. Thus, this study eval
uated vWF plasma levels in relation to renal and retinal structural ab
normalities in NIDDM patients with MA. Kidney biopsies, fundoscopy and
measures of vWF plasma levels were performed in 32 NIDDM patients wit
h MA. These patients were allocated to two renal structural categories
: A) Without renal structural abnormalities (C I, n = 10): normal or n
ear-normal renal structure, and B) With renal structural abnormalities
(n = 22), further divided into: C II (n = 12) with typical diabetic n
ephropathology, predominantly glomerulopathy, and C III (n = 10) with
atypical patterns of renal injury (more advanced tubulo-interstitial a
nd arteriolar than glomerular changes). vWF plasma levels were signifi
cantly higher in category B (C II: 195 +/- 49 % and C III: 161 +/- 46
%) than in category A (C I: 119 +/- 42 %), (chi-square, p < 0.05). Dia
betic retinopathy was also related to vWF plasma levels (ANOVA, p < 0.
05). These data suggest that there are two types of MA in NIDDM: one a
ssociated with increased vWF levels, established renal injury and freq
uently retinopathy, and the other characterized by normal vWF levels,
normal renal structure and absent or mild diabetic retinopathy, We pro
pose that vWF plasma levels in NIDDM patients with MA may help to iden
tify patients with important renal structural changes, increased retin
opathy risk and, perhaps, generalised endothelial dysfunction. Whether
vWF plasma levels predict end-stage renal disease and cardiovascular
events deserves longitudinal studies.