H. Trachtman et al., ISOLATED PROTEINURIA IN CHILDREN - NATURAL-HISTORY AND INDICATIONS FOR RENAL BIOPSY, Clinical pediatrics, 33(8), 1994, pp. 468-472
The significance of isolated proteinuria in pediatric patients is unce
rtain. Therefore, we retrospectively studied all children evaluated fo
r this urinary abnormality during the 6-year period from 1986 to 1992.
Thirty-one patients (19 males), age 2 to 20 years, were identified as
having isolated proteinuria that had persisted for a mean interval of
9.6 +/- 1.9 (SEM) months. The diagnosis was based upon the presence o
f a urine protein:creatinine ratio >0.2 in an early-morning specimen.
None of the patients had hematuria, edema, or azotemia. Seventeen chil
dren underwent a renal biopsy. There was no difference between the pat
ients who were biopsied and those who were not with respect to age, ma
gnitude of proteinuria, glomerular filtration rate (GFR), or serum alb
umin and cholesterol concentrations. The renal histopathology revealed
focal segmental glomerulosclerosis (FSGS) (n = 8), membranous nephrop
athy (n = 1), postinfectious nephritis (n = 2),focal global glomerulos
clerosis (FGGS) (n = 1), and normal kidney tissue (n = 5). Twelve of t
he patients who did not undergo a kidney biopsy and four of the five c
hildren with a normal renal biopsy were followed for at least 12 month
s; there was complete resolution of the proteinuria in 11 (69%) of the
se patients. The level of proteinuria did not predict the presence or
absence of important kidney disease. However, if isolated proteinuria
persists for more than 1 year, it is then unlikely to spontaneously re
mit and a renal biopsy is indicated to clarify the nature of any under
lying glomerulopathy. In children with isolated proteinuria of 1 year'
s duration, there is a high likelihood of detecting significant renal
pathology that may adversely affect their long-term prognosis.