Long-Term Outcomes in Nephrotic Syndrome by Kidney Biopsy Diagnosis and Proteinuria

Key Points In nephrotic syndrome, diagnosis was associated with kidney failure risk: very high in monogenic cases, substantial in FSGS, and less but not zero in minimal change disease. Early control of proteinuria was associated with lower kidney failure risk, and in FSGS levels <1.5 g/g are associated with good kidney outcomes at 10 years. Monogenic nephrotic syndrome cases had very high proteinuria and rapid progression to kidney failure with little response to current treatments. Background The UK National Registry of Rare Kidney Diseases Idiopathic Nephrotic Syndrome cohort includes adults and children with genetic nephrotic syndrome, FSGS, and minimal change disease. This study examines long-term patient outcomes as a function of kidney biopsy diagnosis and proteinuria control. Methods Two thousand four hundred and sixty-seven adults and 1599 children were followed to establish outcomes including eGFR slope and kidney survival by diagnosis, analyzed as a function of proteinuria from disease onset for FSGS and minimal change disease. Enrollment began in 2010, with follow-up to September 2023. Index date for the survival analyses was date of disease onset. Results The cohort had a median (interquartile range) follow-up of 8.2 (4.3–13.1) years; 30% of patients reached kidney failure or died. In total, 1303 patients had FSGS, 1153 had minimal change disease, and 105 had monogenic nephrotic syndrome. Children showed relatively preserved mean kidney function at disease onset (eGFR >100 ml/min per 1.73 m 2 ), compared with adults (FSGS 61 ml/min per 1.73 m 2 ; minimal change disease 76 ml/min per 1.73 m 2 ). Kidney survival probability (95% confidence interval [CI]) at 10 years varied with diagnosis: genetic 29% (20 to 38), FSGS 58% (55 to 61), minimal change disease 87% (85 to 89) with mean (SD) rates of eGFR loss −26.5 (34.7), −6.2 (14.3), and −1.9 (10.2) ml/min per 1.73 m 2 per year, respectively. FSGS 10-year kidney survival (95% CI) for 6–12 months lowest proteinuria value in complete remission (<0.3 g/g), partial remission (0.3–3.5 g/g), and no remission (>3.5 g/g) was 88% (70 to 96), 65% (50 to 76), and 37% (26 to 48), respectively. Time-averaged proteinuria of <1.5 g/g over 6–24 months from disease onset was associated with 90% 10-year kidney survival. For minimal change disease, patients' 10-year kidney survival (95% CI) stratified by 6–12 months lowest proteinuria value was complete remission 89% (79 to 94), partial remission 75% (51 to 89), and no remission 64% (41 to 81). In FSGS and minimal change disease, 10-year eGFR slope was strongly correlated with absolute levels of proteinuria. Conclusions Kidney outcomes were poor in genetic nephrotic syndrome; in FSGS, outcomes were strongly associated with the proteinuria level. Patients with minimal change disease had better proteinuria control than FSGS and had better outcomes at each proteinuria level.

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Journal
Journal of the American Society of Nephrology
Published
2025-04-17
DOI
https://doi.org/10.1681/asn.0000000610
Citations
9
Primary Topic
Renal Diseases and Glomerulopathies
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article
Field-Weighted Citation Impact
12.88
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article

Long-Term Outcomes in Nephrotic Syndrome by Kidney Biopsy Diagnosis and Proteinuria

Moin A. Saleem, Jonathan Barratt, Retha Steenkamp, Wu Gong et al.
9 citations
Journal of the American Society of Nephrology
Renal Diseases and Glomerulopathies
12.88
article

Long-Term Outcomes in Nephrotic Syndrome by Kidney Biopsy Diagnosis and Proteinuria

Moin A. Saleem, Jonathan Barratt, Retha Steenkamp, Wu Gong, Daniel P. Gale, Neil Turner, David Pitcher, Alex Mercer, Bruce M. Hendry, Fiona Braddon, Katie Wong
article en
9 citations

Abstract

Key Points In nephrotic syndrome, diagnosis was associated with kidney failure risk: very high in monogenic cases, substantial in FSGS, and less but not zero in minimal change disease. Early control of proteinuria was associated with lower kidney failure risk, and in FSGS levels <1.5 g/g are associated with good kidney outcomes at 10 years. Monogenic nephrotic syndrome cases had very high proteinuria and rapid progression to kidney failure with little response to current treatments. Background The UK National Registry of Rare Kidney Diseases Idiopathic Nephrotic Syndrome cohort includes adults and children with genetic nephrotic syndrome, FSGS, and minimal change disease. This study examines long-term patient outcomes as a function of kidney biopsy diagnosis and proteinuria control. Methods Two thousand four hundred and sixty-seven adults and 1599 children were followed to establish outcomes including eGFR slope and kidney survival by diagnosis, analyzed as a function of proteinuria from disease onset for FSGS and minimal change disease. Enrollment began in 2010, with follow-up to September 2023. Index date for the survival analyses was date of disease onset. Results The cohort had a median (interquartile range) follow-up of 8.2 (4.3–13.1) years; 30% of patients reached kidney failure or died. In total, 1303 patients had FSGS, 1153 had minimal change disease, and 105 had monogenic nephrotic syndrome. Children showed relatively preserved mean kidney function at disease onset (eGFR >100 ml/min per 1.73 m 2 ), compared with adults (FSGS 61 ml/min per 1.73 m 2 ; minimal change disease 76 ml/min per 1.73 m 2 ). Kidney survival probability (95% confidence interval [CI]) at 10 years varied with diagnosis: genetic 29% (20 to 38), FSGS 58% (55 to 61), minimal change disease 87% (85 to 89) with mean (SD) rates of eGFR loss −26.5 (34.7), −6.2 (14.3), and −1.9 (10.2) ml/min per 1.73 m 2 per year, respectively. FSGS 10-year kidney survival (95% CI) for 6–12 months lowest proteinuria value in complete remission (<0.3 g/g), partial remission (0.3–3.5 g/g), and no remission (>3.5 g/g) was 88% (70 to 96), 65% (50 to 76), and 37% (26 to 48), respectively. Time-averaged proteinuria of <1.5 g/g over 6–24 months from disease onset was associated with 90% 10-year kidney survival. For minimal change disease, patients' 10-year kidney survival (95% CI) stratified by 6–12 months lowest proteinuria value was complete remission 89% (79 to 94), partial remission 75% (51 to 89), and no remission 64% (41 to 81). In FSGS and minimal change disease, 10-year eGFR slope was strongly correlated with absolute levels of proteinuria. Conclusions Kidney outcomes were poor in genetic nephrotic syndrome; in FSGS, outcomes were strongly associated with the proteinuria level. Patients with minimal change disease had better proteinuria control than FSGS and had better outcomes at each proteinuria level.

Journal of the American Society of NephrologyVol. 36(7)
University of Leicester (GB), Leicester General Hospital (GB), Bristol Royal Hospital for Children (GB), University of Bristol (GB), Kidney Care UK (GB), Therapeutics Clinical Research (US), University College London (GB), University of Edinburgh (GB)
Good health and well-being
Openalex Percentile: Top 1%
Renal Diseases and Glomerulopathies
12.88
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