Diabetic nephropathy is the only increasing cause of renal failure in
the Western world. It affects a large proportion of both insulin-depen
dent (IDDM) and non-insulin-dependent diabetic (NIDDM) patients. A cri
tical stage in the development of diabetic renal disease is the onset
of microalbuminuria, defined as an albumin excretion rate of 30 to 300
mg/day. Microalbuminuria predicts progression to renal failure and ea
rly cardiovascular mortality in both IDDM and NIDDM patients. Microalb
uminuria is associated with a constellation of other risk factors for
small and large vessel damage which include raised blood pressure, poo
r glycemic control, plasma lipid and clotting factor abnormalities, le
ft ventricular hypertrophy, and insulin resistance. Treatment with ang
iotensin-converting enzyme inhibitors corrects microalbuminuria and pr
events progression to persistent proteinuria. Good blood glucose contr
ol significantly reduces the risk of progression from normoalbuminuria
to microalbuminuria. The treatment of microalbuminuria appears highly
cost-beneficial and substantially increases life expectancy. The deve
lopment of microalbuminuria, for which all diabetic patients aged 12 t
o 70 years should be screened, should alert the physician to set in mo
tion a program of assessment, monitoring, and correction of all risk f
actors for renal and cardiovascular disease.