O ur current state of knowledge regarding the predictive value and pathomechanistic importance of proteinuria in progressive renal failure has been established mostly by studying glomerular disorders usually acquired in adult life, such as diabetic or IgA nephropathy. Chronic kidney disease (CKD) in children is caused by a quite different spectrum of underlying disorders. At least 60% of children with CKD have a variety of hypo-and dysplastic malformations of the kidneys commonly associated with refluxive or obstructive uropathies and termed "congenital anomalies of the kidneys and urinary tract" (CAKUT). Primary glomerulopathies account for only 15 to 20% of pediatric CKD cases and comprise mainly inherited structural disorders of the podocytes. The rest of the spectrum is formed by various rare disorders, including hereditary kidney disorders such as nephronophthisis or Alport syndrome; systemic diseases involving the kidneys, such as hemolytic uremic syndrome, lupus erythematosus, cystinosis, and oxalosis; and development of CKD after peri-or postnatal acute kidney injury.Few studies have addressed the prevalence, extent, covariates, and prognostic value of proteinuria in this heterogeneous pediatric population. In this issue of CJASN, Wong et al.(1) characterize proteinuria in a large, unselected pediatric cohort followed in the Chronic Kidney Disease in Children (CKiD) Study. Their report is remarkable for a large sample size and high methodologic quality applied in a multicenter effort, including GFR assessments by iohexol clearance and centralized proteinuria measurements. The cross-sectional analysis at time of enrollment revealed that 75% of pediatric patients with stages 2 through 4 CKD exhibit some degree of proteinuria, although only 14% reach the nephrotic range. Notably, in 81% of the children with "significant" and 52% of those with nephrotic-range proteinuria, CKD was due to nonglomerular disorders, although absolute urinary protein/creatinine levels were 140% higher on average in patients with glomerular diagnoses. Hence, the data provided by Wong et al. provide demographic evidence that the majority of children with proteinuria have nephropathies that do not primarily affect the glomerulus. Although the authors did not provide a more detailed analysis of the relative degree of proteinuria in individual nonglomerular nephropathies, it can be assumed that the bulk of patients had CAKUT-type disorders.Irrespective of the nature of the underlying disease, the most important predictor of proteinuria was a low level of GFR. The cross-sectional nature of this study does not allow differentiation of whether heavy proteinuria caused a more rapid progression of CKD or whether proteinuria generally tends to increase with advancing CKD; however, several prospective observational studies of children have provided evidence for an independent link between proteinuria and progression even in children with nonglomerular nephropathies (2-4). As in adult nephropathies, the renal risk conferred by even moderate pr...