NDT Advance Access published online on September 12, 2006
Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfl237
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Universidade de São Paulo, Medicina-Nefrologia, São Paulo, Brazil
* To whom correspondence should be addressed. Background. The Paulista Registry of Glomerulopathies was created in May 1999 and comprises several centres of São Paulo, the most populous Brazilian State, that concentrates people from all regions of the country who look for health care. Methods. This report includes data from 2086 patients from Brazil submitted to renal biopsy due to the presumed diagnosis of glomerular diseases, registered prospectively since May 1999 until January 2005. Data were collected by the integrants of the 11 centres involved, utilizing a standardized questionnaire. Results. The mean age of the patients was 34.5 ± 14.6 years. Primary glomerular diseases were more frequent in males (55.1%) than in females; on the other hand, secondary glomerular diseases were more frequent in females (71.8%). The most common clinical presentation was nephrotic syndrome and the frequency of hypertension, at this time, was 55.5%. There was a predominance of indication of biopsies in the third, fourth and fifth decades of life. The most common primary glomerular diseases were focal and segmental glomerulosclerosis (29.7%), followed by membranous nephropathy (20.7%), IgA nephropathy (17.8%), minimal change disease (9.1%), membranoproliferative glomerulonephritis (7%), crescentic glomerulonephritis (4.1%), advanced chronic glomerulopathy (4%), non-IgA mesangial glomerulonephritis (3.8%), diffuse proliferative glomerulonephritis (2.5%), focal segmental proliferative glomerulonephritis (1%) and others (0.3%). The most frequent secondary glomerular disease was lupus nephritis, corresponding to 66.2% of the cases, followed by post-infectious glomerulonephritis (12.5%), diabetic nephropathy (6.2%), diseases associated to paraproteinaemia (4.9%), hereditary diseases (4.6%), vasculitis (3.2%), malignancies (0.9.%), secondary focal segmental glomerulosclerosis (0.6%) and others (0.9%). Conclusion. Focal segmental glomerulosclerosis was the most frequent primary glomerular disease, followed by membranous nephropathy and IgA nephropathy. Lupus nephritis predominated over all the other secondary glomerular diseases. First and second authors had equivalent participation in the elaboration of this article.
Received March 31, 2006
Accepted April 3, 2006
Original Article
Paulista registry of glomerulonephritis: 5-year data report
Patricia Malafronte 1, Gianna Mastroianni-Kirsztajn 2 *, Gustavo N. Betônico 3, João Egídio Romão Jr 4, Maria Almerinda R. Alves 5, Maria Fernanda Carvalho 6, Osvaldo M. Viera Neto 7, Ricardo A. M. Cadaval 8, Ronaldo R. Bérgamo 9, Viktória Woronik 1, Yvoty A. S. Sens 10, Mauro S. M. Marrocos 11, and Rui T. Barros 1
2 Universidade Federal de São Paulo, Medicina-Nefriligia, São Paulo, Brazil
3 Universidade do Oeste Paulista-UNOESTE, Medicina-Nefriligia, Presidente Prudente, Brazil
4 Hospital da Beneficência Portuguesa de São Paulo, Medicina-Nefrologia, São Paulo, Brazil
5 Universidade Estadual de Campinas, Medicina-Nefrologia, Campinas, Brazil
6 Universidade Estadual Paulista-Botucatu, Medicina-Nefrologia, Botucatu, Brazil
7 Universidade de São Paulo-Ribeirão Preto, Medicina-Nefrologia, Ribeirão Preto, Brazil
8 Pontifícia Universidade Católica de São Paulo-Sorocaba, Medicina-Nefrologia, Sorocaba, Brazil
9 Faculdade de Medicina do ABC, Medicina-Nefrologia, Santo André, Brazil
10 Faculdade de Ciências Médicas da Santa Casa de São Paulo, Medicina-Nefrologia, São Paulo, Brazil
11 Universidade de São Paulo-Hospital Universitário, Medicina-Nefrologia, São Paulo, SP, Brazil
Gianna Mastroianni-Kirsztajn, E-mail: giannamk{at}uol.com.br
![]()
Abstract ![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
B. W. J. van Rensburg, A. M. van Staden, G. J. Rossouw, and G. Joubert The profile of adult nephrology patients admitted to the Renal Unit of the Universitas Tertiary Hospital in Bloemfontein, South Africa from 1997 to 2006 Nephrol. Dial. Transplant., October 28, 2009; (2009) gfp535v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. B. Hanko, R. N. Mullan, D. M. O'Rourke, P. T. McNamee, A. P. Maxwell, and A. E. Courtney The changing pattern of adult primary glomerular disease Nephrol. Dial. Transplant., October 1, 2009; 24(10): 3050 - 3054. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. P. McQuarrie, B. Mackinnon, B. Young, L. Yeoman, G. Stewart, S. Fleming, S. Robertson, K. Simpson, J. Fox, C. C. Geddes, et al. Centre variation in incidence, indication and diagnosis of adult native renal biopsy in Scotland Nephrol. Dial. Transplant., May 1, 2009; 24(5): 1524 - 1528. [Abstract] [Full Text] [PDF] |
||||
![]() |
F.-d. Zhou, M.-h. Zhao, W.-z. Zou, G. Liu, and H. Wang The changing spectrum of primary glomerular diseases within 15 years: A survey of 3331 patients in a single Chinese centre Nephrol. Dial. Transplant., March 1, 2009; 24(3): 870 - 876. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Lopez-Gomez, F. Rivera, and on behalf of Spanish Registry of Glomerulonephriti Renal Biopsy Findings in Acute Renal Failure in the Cohort of Patients in the Spanish Registry of Glomerulonephritis Clin. J. Am. Soc. Nephrol., May 1, 2008; 3(3): 674 - 681. [Abstract] [Full Text] [PDF] |
||||

