Wg. Guder et al., Physiopathology of proteinuria and laboratory diagnostic strategy based onsingle protein analysis, CLIN CH L M, 36(12), 1998, pp. 935-939
A quantification of proteins of different molecular size has been shown to
be useful in characterizing the mechanism and medical causes of proteinuria
. By analyzing urine albumin, alpha(1)-microglobulin, immunoglobulin G and
alpha(2)-macroglobulin together with total protein, prerenal, glomerular, t
ubular and postrenal causes of proteinuria can be detected and differentiat
ed by their specific urine protein patterns. Using automated turbidimetric
procedures, prerenal proteinurias are characterized by an albumin/total pro
tein ratio below 0.4. Tubulo-interstitial diseases which are negative in th
e protein test strip procedure are detected and clearly differentiated from
other causes of proteinuria by their high alpha(1)-microglobulin/albumin r
atios. In postrenal proteinuria, alpha(2)-macroglobulin proved to be a usef
ul marker, when albumin excretion exceeds 100 mg/l urine. This protein exhi
bits plasma-like ratios to albumin in postrenal causes, whereas it is much
lower in renal proteinurias.
The new strategy, which has been evaluated in more than 500 clinically and
partly histologically proven cases of renal diseases, more sensitively dete
cts glomerular and tubulo-interstitial diseases when applied in urine scree
ning and allows us to distinguish all clinically important causes from anal
ysis of a morning spot urine sample.