Literature DB >> 26084617

A predictive model of progressive chronic kidney disease in idiopathic nephrotic syndrome.

Ana Carmen Quaresma Mendonça1, Eduardo Araújo Oliveira1, Brunna Pinto Fróes1, Lauro Damasceno Carvalho Faria2, Juliana Silva Pinto2, Maira Melo Ibrahim Nogueira2, Gabriella Oliveira Lima2, Priscila Isa Resende2, Natália Silva Assis2, Ana Cristina Simões E Silva1, Sérgio Veloso Brant Pinheiro3.   

Abstract

BACKGROUND: There are limited data on the risk factors for chronic kidney disease (CKD) in children with idiopathic nephrotic syndrome (INS). This retrospective cohort study aimed to develop a predictive model for CKD progression in children with INS.
METHODS: Between 1970 and 2012, a total of 294 patients with INS were followed up. The primary outcome was progression to CKD stage 3 or higher. A predictive model was developed using a Cox proportional hazards model. A score was calculated using b-coefficients and summing up points assigned to each significant variable. Prognostic score was grouped into categories: low risk, medium risk, and high risk.
RESULTS: Median follow-up was 6.9 years. Median renal survival was 26.1 years and probability of CKD stage 3 or higher was 8% in 10 years. Multivariate analysis showed that the most accurate model included initial age, hematuria, and steroid resistance. Accuracy was high with a c-statistic of 0.95 (95% confidence interval [CI] 0.91-0.99), 0.92 (95% CI 0.88-0.96), and 0.92 (95% CI 0.87-0.97) at 2, 5, and 10 years of follow-up respectively. By survival analysis, 10-year renal survival was 100% for the low-risk and 95% for the medium-risk group, while 40% of high-risk patients would exhibit CKD stage 3 or higher (P < 0.001).
CONCLUSIONS: Our predictive model of CKD may contribute to the early identification of a subgroup of INS patients at a high risk of renal dysfunction.

Entities:  

Keywords:  Chronic kidney disease; End-stage renal disease; Focal segmental glomerulosclerosis; Minimal change nephrotic syndrome; Nephrotic syndrome; Predictive model

Mesh:

Year:  2015        PMID: 26084617     DOI: 10.1007/s00467-015-3136-0

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  46 in total

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