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Published on: August 19, 2020
Predictive factors of chronic kidney disease in primary focal segmental glomerulosclerosis
Marcelo M Abrantes1, Luis Sergio B Cardoso, Eleonora M Lima
1Pediatric Nephrourology Unit, Hospital das Clínicas, School of Medicine, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Insights
Predictors of chronic kidney disease (CKD) in children with focal segmental glomerulosclerosis (FSGS) include age, creatinine levels, and steroid response. Early identification of these factors aids in managing pediatric kidney disease progression.
Area of Science:
- Pediatric Nephrology
- Glomerular Diseases
- Renal Pathology
Background:
- Focal segmental glomerulosclerosis (FSGS) is a significant cause of nephrotic syndrome in children, with 75% exhibiting steroid resistance.
- Identifying predictors of chronic kidney disease (CKD) is crucial for managing pediatric FSGS patients.
Purpose of the Study:
- To evaluate predictive factors for the development of CKD in children diagnosed with biopsy-proven FSGS.
- To establish models predicting CKD from symptom onset and from renal biopsy time.
Main Methods:
- Retrospective review of 110 pediatric FSGS patients (1972-2004).
- Analysis of renal survival using Kaplan-Meier and Cox regression models.
- Development of two multivariate models to identify CKD predictors.
Main Results:
- 21.8% of patients progressed to CKD over a mean 10-year follow-up.
- Baseline predictors of CKD: age >6.5 years, creatinine >1 mg/dl, and non-response to steroids.
- Renal biopsy predictors of CKD: hematuria and creatinine >0.8 mg/dl.
Conclusions:
- Age, creatinine levels, hematuria, and steroid response are key predictors of CKD in pediatric FSGS.
- These findings aid in risk stratification and management strategies for children with FSGS.
Abstract:
Renal histological features of focal segmental glomerulosclerosis (FSGS) are found in 75% of pediatric patients with steroid-resistant nephrotic syndrome. In order to evaluate the predictive factors of chronic kidney disease (CKD), we retrospectively reviewed the records of 110 children with biopsy-proven FSGS admitted between 1972 and 2004. Renal survival was analyzed by the Kaplan-Meier method and Cox's regression model. Two multivariate models were developed: (1) from the onset of symptoms to the occurrence of CKD and (2) from the time of renal biopsy to CKD. Mean follow-up time was 10 years [standard deviation ((SD) 5.5], and 24 patients (21.8%) progressed to CKD. At baseline, after adjustment three variables remained as independent predictors of CKD: age >6.5 years (RR=3.3, 95% CI=1.3-7.8), creatinine >1 mg/dl (RR=2.5, 95% CI=0.97-6.5), and non-response to steroids (RR=7.3, 95% CI=2.7-19.7). In a model with continuous variables only age and non-response to steroids were associated with CKD. At the time of renal biopsy, after adjustment two variables remained as independent predictors of CKD: hematuria (RR=3.0, 95% CI=1.2-7.3) and creatinine >0.8 mg/dl (RR=4.3, 95% CI=1.7-10.6). In a model with continuous variables four factors predicted CKD: age, creatinine, hematuria, and percentage of global sclerosis.
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