Microalbuminuria is a marker of manifestation of diabetic nephropathy.
Experimental data give evidence for the underlying mechanisms in the
development of diabetic nephropathy. Therapeutic measures have develop
ed from which some are still experimental some are already in clinical
practice. A strict control of blood glucose is able to prevent diabet
ic nephropathy in IDDM which is followed by lower morbidity and mortal
ity. Use of ACE-Inhibitors should lead to an effective blood pressure
control and a restriction of proteinuria in the case of normotonia. Pr
otein restriction of 0.8 g per kg body weight is recommended. Aldose r
eductase inhibitors block the polyol pathway resulting a lower intrace
llular accumulation of sorbitol. Aminoguanidin demonstrates inhibitory
effects on advanced glycosylated end products. Both substances are in
phase II/III studies. Experimental data suggest a broadening of the a
rmentarium against diabetic nephropathy, e.g. antibodies or selective
inhibitors of Amadori product, cytokine receptor antibodies or selecti
ve inhibitors of proteinkinase C. The clinical relevance has to be sho
wn by studies in the future. Treatment of comorbid factors like hypert
ension, smoking, hyperlipidemia and infections should always play an i
mportant role in the therapy of diabetic nephropathy.