Abstract
Atypical membranoproliferative glomerulonephritis (MPGN) has been reported to have a good prognosis when treated with corticosteroids. However, this recommendation is based on uncontrolled trials and is associated with many complications. The purpose of our study is to determine whether steroid therapy is indicated for atypical MPGN. The cases of seven patients with atypical MPGN are reported in this study. Urinary abnormalities of five of them were detected by urine screening at school, of two because of macrohematuria. Hypocomplementemia was noted in six patients. All but one patient were treated without corticosteroids, and five with angiotensin-converting enzyme inhibitors (ACEI) and/or the Chinese herbal medicine Sairei-to (TJ-114). One patient recovered spontaneously from proteinuria and was therefore not treated, and one who developed severe proteinuria during observation was treated with corticosteroids. After an average follow-up period of 10.0 years, five patients showed normal urinary findings, one had hematuria and one proteinuria. At the most recent follow-up, the renal function of all patients remained within the normal range, and serum C3 had returned to normal levels in five out of six. These findings suggest that the indication of steroid therapy for atypical MPGN should be re-examined, since most of the patients with atypical MPGN seem to have an excellent prognosis without treatment with corticosteroids.
Similar content being viewed by others
References
Habib R (1973) Classification of glomerulonephritis based on morphology. In: Kincaid-Smith P, Mathew TH, Becker EL (eds) Glomerulonephritis morphology, natural history, and treatment. John Wiley and Sons, New York, pp17–41
Strife CF, McAdams AJ, West CD (1982) Membranoproliferative glomerulonephritis characterized by focal, segmental proliferative lesions. Clin Nephrol 18:9–16
Watson AR, Poucell S, Thorner P, Arbus GS, Rance CP, Baumal R (1984) Membranoproliferative glomerulonephritis type I in children: correlation of clinical features with pathologic subtypes. Am J Kidney Dis 4:141–146
Yoshikawa N, Yoshiara S, Yoshiya K, Matsuo T, Matsuyama S, Okada S (1988) Focal and diffuse membranoproliferative glomerulonephritis in children. Am J Nephrol 8:102–107
Hattori M, Yamaguchi H, Kawaguchi H, Kono M, Kubota R, Tsunoda Y, Takeda Y, Ito K (1990) Clinico-pathological study of children with membranoproliferative glomerulonephritis (MPGN) characterized by focal, segmental lesion (in Japanese). Jpn J Pediatr 94:2407–2416
Iitaka K, Nakamura S, Moriya S, Motoyama O, Sakai T (2003) Focal segmental membranoproliferative glomerulonephritis in children. Pediatr Nephrol 18:1000–1004
McAdams AJ, McEnery PT, West CD (1975) Mesangiocapillary glomerulonephritis: changes in glomerular morphology with long-term alternate-day prednisone therapy. J Pediatr 86:23–31
McEnery PT, McAdams AJ, West CD (1980) Membranoproliferative glomerulonephritis: improved survival with alternate day prednisone therapy. Clin Nephrol 13:117–124
Warady BA, Guggenheim SJ, Sedman A, Lum GM (1985) Prednisone therapy of membranoproliferative glomerulonephritis in children. J Pediatr 107:702–707
Mota-Hernandez F, Gordillo-Paniagua G, Munoz-Arizpe R, Lopez-Arriaga JA, Barboza-Madueno L (1985) Prednisone versus placebo in membranoproliferative glomerulonephritis: long-term clinicopathological correlations. Int J Pediatr Nephrol 6:25–28
Ford DM, Briscoe DM, Shanley PF, Lum GM (1992) Childhood membranoproliferative glomerulonephritis type I: limited steroid therapy. Kidney Int 41:1606–1612
Yamazaki Y, Shimada M, Tateishi S, Shimizu T, Nomura Y (1997) Atypical Membranoproliferative glomerulonephritis (MPGN) in children—effect of methylprednisolone pulse therapy (MPT) (in Japanese). Jpn J Pediatr 101:819–824
International Study of Kidney Disease in Children (1982) Alternate-day steroid therapy in membranoproliferative glomerulonephritis: a randomized controlled clinical trial. Kidney Int 21:150
McEnery PT, McAdams AJ, West CD (1985) The effect of prednisone in a high-dose, alternate-day regimen on the natural history of idiopathic membranoproliferative glomerulonephritis. Medicine (Baltimore) 64:401–424
Kawasaki Y, Suzuki J, Nozawa R, Suzuki H (2002) Efficacy of school urinary screening for membranoproliferative glomerulonephritis type 1. Arch Dis Child 86:21–25
Iitaka K, Ishidate T, Hojo M, Kuwao S, Kasai N, Sakai T (1995) Idiopathic membranoproliferative glomerulonephritis in Japanese children. Pediatr Nephrol 9:272–277
Hebert LA, Cosio FG, Neff JC (1991) Diagnostic significance of hypocomplementemia. Kidney Int 39:811–821
Matsell DG, Roy S III, Tamerius JD, Morrow PR, Kolb WP, Wyatt RJ (1991) Plasma terminal complement complexes in acute poststreptococcal glomerulonephritis. Am J Kidney Dis 17:311–316
Churg J, Bernsten J, Glassock RJ (1995) Renal disease, classification and atlas of glomerular disease. Igaku-Shoin, Tokyo, New York, pp 107–131
Churg J, Habib R, White RH (1970) Pathology of the nephrotic syndrome in children: a report for the International Study of Kidney Disease in Children. Lancet 760:1299–1302
Ginsberg JM, Chang BS, Matarese RA, Garella S (1983) Use of single voided urine samples to estimate quantitative proteinuria. N Engl J Med 309:1543–1546
Houser M (1984) Assessment of proteinuria using random urine samples. J Pediatr 104:845–848
Shaw AB, Risdon P, Lewis-Jackson JD (1983) Protein creatinine index and Albustix in assessment of proteinuria. Br Med J (Clin Res Ed) 287:929–932
McEnery PT (1990) Membranoproliferative glomerulonephritis: the Cincinnati experience—cumulative renal survival from 1957 to 1989. J Pediatr 116:109–114
Habib R, Levy M, Gubler MC (1976) Membranoproliferative glomerulonephritis: morphological patterns, immunofluorescence and complement studies. Proceedings of the 11th Congress of the International Academy of Pathology, Washington DC, pp 106
Levy M, Gubler M, Habib R (1979) New concepts on membranoproliferative glomerulonephritis. In: Kincaid-Smith P, d’Apice AJF, Atkins RC (eds) Progress in glomerulonephritis. John Wiley and Sons, New York, pp 177–205
Kitagawa T (1988) Lessons learned from the Japanese nephritis screening study. Pediatr Nephrol 2:256–263
Kincaid-Smith P (1972) The treatment of chronic mesangiocapillary (membranoproliferative) glomerulonephritis with impaired renal function. Med J Aust 9:587–592
Lewis EJ, Hunsicker LG, Bain RP, Rohde RD (1993) The effect of angiotensin-converting-enzyme inhibitor on diabetic nephropathy. The Collaborative Study Group. N Engl J Med 329:1456–1462
Ruggenenti P, Perna A, Gherardi G, Garini G, Zoccali C, Salvadori M, Scolari F, Schena FP, Remuzzi G (1999) Renoprotective properties of ACE-inhibition in non-diabetic nephropathies with non-nephrotic proteinuria. Lancet 354:359–364
Russo D, Pisani A, Balletta MM, De Nicoli L, Savino FA, Andreucci M, Minutolo R (1999) Additive antiproteinuric effect of converting enzyme inhibitor and losartan in normotensive patients with IgA nephropathy. Am J Kidney Dis 33:851-856
Gansevoort RT, de Zeeuw D, de Jong PE (1994) Is the antiproteinuric effect of ACE inhibition mediated by interference in the renin-angiotensin system? Kidney Int 45:861–867
Butani L (2003) Remission of membranoproliferative nephritis with angiotensin converting enzyme inhibition and receptor blockade. Pediatr Nephrol 18:1199
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Fujita, T., Nozu, K., Iijima, K. et al. Long-term follow-up of atypical membranoproliferative glomerulonephritis: are steroids indicated?. Pediatr Nephrol 21, 194–200 (2006). https://doi.org/10.1007/s00467-005-2074-7
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00467-005-2074-7