Mg. Costigan et al., ORIGIN AND SIGNIFICANCE OF URINARY N-ACETYL-BETA,D-GLUCOSAMINIDASE (NAG) IN RENAL PATIENTS WITH PROTEINURIA, Clinica chimica acta, 255(2), 1996, pp. 133-144
In patients with proteinuria, indices of tubular damage are unreliable
since filtered plasma enzymes could contribute to tubular enzymuria.
Previous work has suggested the existence of various forms of the 'A'
isoenzyme of N-acetyl-beta,D-glucosaminidase (NAG), one of which could
be kidney specific and thus a useful marker of renal tubular damage.
By using fast protein liquid chromatography, two forms of the 'A' isoe
nzyme, 'A1' and 'A2' were separated in human urine, plasma and kidney
tissue. The isoenzyme profile in pathological urine resembled that see
n in kidney tissue, the 'A2' isoenzyme predominating. The ratio A2/A1
in the urine of renal patients was significantly greater than in the p
lasma of renal patients, end-stage renal failure patients and healthy
volunteers. There was no difference in the plasma ratios of the three
groups studied. The clearances of total NAG, 'A1' and 'A2' isoenzymes
were all greater than that of the lower molecular weight protein trans
ferrin. This indicates that the origin of urinary NAG in patients with
proteinuria is from the kidney itself. Thus, analysis of urinary NAG
and its isoenzymes may be of benefit as an early predictor of renal tu
bular damage and may also be useful as a non-invasive indicator of dis
ease progression.