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Improved renal survival in Japanese children with IgA nephropathy
Nahoko Yata1, Koichi Nakanishi, Yuko Shima
1Department of Pediatrics, Wakayama Medical University, 811-1 Kimiidera, Wakayama 641-8509, Japan.
Insights
Treatment advancements have improved long-term renal survival for Japanese children with IgA nephropathy (IgA-N). Outcomes were significantly better after 1990, especially for severe cases, indicating a positive trend in pediatric kidney disease management.
Area of Science:
- Pediatric Nephrology
- Immunology
- Clinical Epidemiology
Background:
- IgA nephropathy (IgA-N) is a common pediatric kidney disease.
- Treatment strategies for IgA-N in Japanese children evolved in the 1990s with the introduction of ACE inhibitors and steroids.
- Long-term outcomes for pediatric IgA-N in Japan have not been extensively evaluated.
Purpose of the Study:
- To assess the long-term renal survival trends in Japanese children diagnosed with IgA nephropathy.
- To determine if treatment advancements since the 1990s have improved outcomes for pediatric IgA-N.
- To identify factors influencing end-stage renal disease (ESRD)-free survival in this cohort.
Main Methods:
- Retrospective cohort study of 500 children diagnosed with IgA-N between 1976 and 2004.
- Division of the study period into two groups: 1976-1989 and 1990-2004.
- Kaplan-Meier analysis for actuarial renal survival and logrank test for comparisons; Cox proportional hazard model for multivariate analysis.
Main Results:
- Overall actuarial renal survival was 96.4% at 10 years, 84.5% at 15 years, and 73.9% at 20 years.
- Renal survival was significantly better in the 1990-2004 period compared to 1976-1989 (p=0.008).
- A marked improvement in renal survival was observed in patients with severe IgA-N (p=0.0003), with diagnosis year being an independent predictor of ESRD-free survival.
Conclusions:
- Long-term renal survival has significantly improved in Japanese children with IgA nephropathy since the 1990s.
- The improved outcomes are likely associated with changes in treatment protocols, including the use of ACE inhibitors and steroids.
- Diagnosis year is a crucial factor for predicting long-term renal outcomes in pediatric IgA-N.
Abstract:
Since the beginning of the 1990s, Japanese medical practitioners have extensively prescribed angiotensin-converting enzyme (ACE) inhibitors for children with mild IgA nephropathy (IgA-N) and steriods for those with severe IgA-N. We have performed a retrospective cohort study to clarify whether the long-term outcome has improved in Japanese children with IgA-N. Renal survival was defined as the time from onset to end-stage renal disease (ESRD). We divided the study period into two time periods based on the occurrence of the initial renal biopsy:1976-1989 and 1990-2004. Actuarial survivals were calculated by Kaplan-Meier method, and comparisons were made with the logrank test. The Cox proportional hazard model was used for multivariate analysis. Between 1976 and 2004, 500 children were diagnosed as having IgA-N in our hospitals. The actuarial renal survival from the time of apparent disease onset was 96.4% at 10 years, 84.5% at 15 years and 73.9% at 20 years. Renal survival in the 1990-2004 period was significantly better than that in 1976-1989 (p=0.008), and a marked improvement in renal survival in patients with severe IgA-N was also observed (p=0.0003). Multivariate analysis indicated that diagnosis year was a significant factor for ESRD-free survival independently of baseline characteristics. The results of this study show that there has been an improvement in terms of renal survival in Japanese children with IgA-N.
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