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Assessment of Kidney Function in Mouse Models of Glomerular Disease
Published on: June 30, 2018
Evidence-based assessment of treatment options for children with IgA nephropathies
1Le Bonheur Children's Medical Center and The Center for Health Policy , University of Tennessee Health Science Center, Memphis 38103, USA.
Insights
Current treatments for IgA nephropathies in children lack high-level evidence. More rigorous randomized controlled trials are needed to establish effective therapies for idiopathic IgA nephropathy (IgAN) and Henoch-Schonlein purpura nephritis (HSPN).
Area of Science:
- Pediatric Nephrology
- Immunology
- Clinical Evidence Evaluation
Background:
- IgA nephropathies, including idiopathic IgA nephropathy (IgAN) and Henoch-Schonlein purpura nephritis (HSPN), are significant causes of kidney disease in children.
- Current therapeutic strategies lack robust evidence from high-quality studies.
Purpose of the Study:
- To critically evaluate existing evidence on therapeutic interventions for pediatric IgA nephropathies.
- To identify outcome markers most relevant to predicting progressive renal failure.
Main Methods:
- Systematic review and evidence-based evaluation of published studies on IgAN and HSPN treatments in children.
- Focus on studies utilizing outcome markers strongly associated with renal failure progression.
Main Results:
- No treatment for pediatric IgAN or HSPN has demonstrated efficacy through high-level evidence (Level 1 randomized controlled trials).
- Some evidence supports corticosteroid use, but findings are conflicting.
- No convincing evidence supports fish oil, ACE inhibitors, or tonsillectomy for these conditions.
Conclusions:
- There is a critical need for well-designed randomized controlled trials in pediatric IgA nephropathies.
- Current treatment approaches require further validation to ensure efficacy and safety in children.
Abstract:
We present an evidence-based evaluation of published data on therapy for children with various presentations of the IgA nephropathies--idiopathic IgA nephropathy (IgAN) and Henoch-Schonlein purpura nephritis (HSPN). Particular attention has been paid to the outcome markers used in the studies reviewed, with the best evidence provided by markers highly associated with progressive renal failure. No treatment modality for either IgAN or HSPN in pediatric patients has been shown to be effective by a properly designed and administered randomized controlled trial (i.e., the highest level of evidence--level 1). Lower levels of evidence support the use of a variety of corticosteroid regimens, often in combination with other agents, although there are some conflicting studies in this area. No convincing evidence has been published to date to support the use of fish oil, angiotensin-converting enzyme inhibitors or tonsillectomy for the treatment of children with IgAN or HSPN. Well designed randomized controlled trials in children with the IgA nephropathies need to be undertaken.
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