Enzymuria as a Marker of Renal Injury and Disease: Studies of N-Acetyl-βglucosaminidase in the General Population and in Patients with Renal Disease

PEDIATRICS ◽  
1978 ◽  
Vol 62 (5) ◽  
pp. 751-760
Author(s):  
Calvin M. Kunin ◽  
Russell W. Chesney ◽  
William A. Craig ◽  
Albert C. England ◽  
Catherine DeAngelis

Urinary excretion of N-acetyl-β-D-glucosaminidase (NAG) was shown to be reproducible in random urine specimens when expressed as the ratio of NAG to milligrams of urinary creatinine. The enzyme/creatinine ratio in 815 healthy people was relatively constant throughout childhood and adult life except for the first two years after birth and in individuals 56 years or greater. High ratios in the young children may be explained by low urinary creatinine excretion probably related to small body mass and reduced glomerular filtration rate at this age. The ratio was increased in adult uremic patients and children and adults with a variety of neurologic and obstructive lesions of the voiding mechanism. The presence of bacteriuria did not appear to increase the ratio. Significant enzymuria (> 2 SD above the mean for age and sex) was detected in 38 of 81 children with well-characterized renal disease. Among patients with predominantly glomerular disorders there was a close relationship between activity of the disease and enzymuria. In patients with tubulointerstitial disease enzymuria was frequent even in the absence of proteinuria. One of the highest enzyme/creatinine ratios was observed in a child with cystinosis. These studies indicate that NAG enzymuria is a sensitive indicator of activity of renal disease and may prove to be a suitable screening test for significant renal disease or injury in childhood.

1970 ◽  
Vol 16 (12) ◽  
pp. 1012-1015 ◽  
Author(s):  
Philip E Cryer ◽  
Jonas Sode

Abstract Urinary creatinine excretion, measured in 96 24-h urine specimens collected from a single subject, was less variable (CV, 9.3%) than daily urine volume (CV, 20.7%). However, a small variation in measured creatinine excretion did exist, since the observed CV of 9.3% was not explicable either on the basis of analytical error (CV for replicate determinations, 1.1%) or of collection error. Thus, 24-h urinary creatinine excretion is not constant. On the other hand, demonstrated variation in creatinine excretion was small, and urinary 17-hydroxycorticosteroids could be validly expressed in mg/g of creatinine. In a given individual, biologic variation in 24-h creatinine excretion is negligible as compared with variation in 17-hydroxycorticosteroid excretion.


2012 ◽  
Vol 31 (2) ◽  
pp. 212-216 ◽  
Author(s):  
Caterina Guidone ◽  
Donatella Gniuli ◽  
Lidia Castagneto-Gissey ◽  
Laura Leccesi ◽  
Eugenio Arrighi ◽  
...  

PEDIATRICS ◽  
1983 ◽  
Vol 71 (1) ◽  
pp. 140-140
Author(s):  
JAMES L. SUTPHEN

In Reply.— The questions posed by Harkavy allow me to expand on the initial presentation of the data in my previous report.1 As documented by numerous previous reports, urinary creatinine excretion does, in fact, reflect body muscle mass.2 Furthermore, it has been documented in older infants that creatinine excretion per kilogram increases with the age, weight, and length of the infant.3 The regression data in my report are not expressed in terms of creatinine per kilogram as the dependent variable as this multiplies the error of creatinine measurement by including the error in weight measurement (hydration states etc).


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