Abstract
Immunoglobulin A (IgA) nephropathy progresses without apparent signs. The only available means of knowing the precise incidence of this disease in children is to analyze data from the school urinary screening system. Students between 6 and 15 years old with IgA nephropathy detected by school urinary screening from 1983 to 1999 in Yonago City, Japan, were examined. In addition, two hospitals with pediatric care units administered a questionnaire and patients with pediatric IgA nephropathy detected by means other than the school urinary screening program were recruited. Of 270,902 children examined by the school urinary screening system, 29 demonstrated suspected chronic nephritis on the basis of abnormal urinalysis and underwent renal biopsy procedures. Among the 29 children, 14 cases of IgA nephropathy were confirmed. During the same period, of the children examined by means other than the school screening program, 20 demonstrated suspected renal disease and underwent renal biopsies. Among these 20 children, 6 cases of IgA nephropathy were diagnosed. In all, 20 cases of pediatric IgA nephropathy were detected over the past 17 years. The incidence rate of pediatric IgA nephropathy was 4.5 cases/year per 100,000 children under 15 years. The incidence of pediatric IgA nephropathy is higher than that of idiopathic nephrotic syndrome.
Similar content being viewed by others
References
Yoshikawa N, Tanaka R, Iijima K (2001) Pathophysiology and treatment of IgA nephropathy in children. Pediatr Nephrol 16:446–457
Kitajima T, Murakami M, Sakai O (1983) Clinicopathological features in Japanese patients with IgA nephropathy. Jpn J Med 22:219–222
Clarkson AR, Seymour AE, Thompson AJ, Haynes WDG, Chan Y-L, Jackson B (1977) IgA nephropathy: a syndrome of uniform morphology, diverse clinical features, and uncertain prognosis. Clin Nephrol 8:459–471
Hood SA, Velosa JA, Holley KE, Donadio JV Jr (1981) IgA-IgG nephropathy: predictive indices of progressive disease. Clin Nephrol 16:55–62
Sissons JGP, Woodrow DF, Curtis JR, Evans DJ, Gover PE, Sloper JC, Peters DK (1975) Isolated glomerulonephritis with mesangial IgA deposits. BMJ 3:611–614
Yoshikawa N, Matsuo T (1984) IgA nephropathy in children. Compr Ther 10:35–41
Yoshikawa N, Iijima K, Ito H (1999) IgA nephropathy in children. Nephron 83:1–12
Schlesinger ER, Schultz HA (1968) The nephrotic syndrome. Its incidence and implications for the community. Am J Dis Child 116:623–632
McKinney PA, Feltbower RG, Brocklebank JT, Fitzpatrick MM (2001) Time trends and ethnic patterns of childhood nephrotic syndrome in Yorkshire, UK. Pediatr Nephrol 16:1040–1044
Wyatt RJ, Julian BA, Baehler RW, Stafford CC, McMorrow RG, Ferguson T, Jackson E, Woodford SY, Miller PM, Kritchevsky S (1998) Epidemiology of IgA nephropathy in central and eastern Kentucky for the period 1975 through 1994. J Am Soc Nephrol 9:553–558
Sehic AM, Gaber LW, Roy S 3rd, Miller PM, Kritchevsky SB, Wyatt RJ (1997) Increased recognition of IgA nephropathy in African-American Children. Pediatr Nephrol 11:435–437
D'Amico G (1987) The commonest glomerulonephritis in the world: IgA nephropathy. QJM 64:709–727
Droz D, Kramar A, Nawer T, Noel LH (1984) Primary IgA nephropathy: prognostic factors. Contrib Nephrol 40:202–207
Wyatt RJ, Kritchevsky SB, Woodford SY, Miller PM, Roy S 3rd, Holland NH, Jackson E, Bishof NA (1995) IgA nephropathy: long-term prognosis for pediatric patients. J Pediatr 127:913–919
Wyatt RJ, Hogg RJ (2001) Evidence-based assessment of treatment options for children with IgA nephropathies. Pediatr Nephrol 16:156–167
Yoshikawa N, Ito H, Sasaki T, Takekoshi Y, Masataka M, Nakagawa K, Nakamura H, Matsuyama M, Seino Y, Takeda Y, Hattori S, Ninomiya M (1999) A controlled trial of combined therapy for newly diagnosed severe childhood IgA nephropathy. J Am Soc Nephrol 10:101–109
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Utsunomiya, Y., Koda, T., Kado, T. et al. Incidence of pediatric IgA nephropathy. Pediatr Nephrol 18, 511–515 (2003). https://doi.org/10.1007/s00467-003-1127-z
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00467-003-1127-z