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Treatment of IgA nephropathy in children: a land without KDIGO guidance
1Fondazione Ricerca Molinette, Regina Margherita Hospital, Turin, Italy. rosanna.coppo@unito.it.
Insights
IgA nephropathy (IgAN) in children requires tailored treatment. Current guidelines are unsuitable, necessitating new models to predict progression and personalize therapy for better outcomes.
Area of Science:
- Pediatric Nephrology
- Glomerular Diseases
- Immunoglobulin A Nephropathy
Background:
- IgA nephropathy (IgAN) in children is a complex condition with varied outcomes, not a rare, benign disease.
- Treatment decisions for IgAN hinge on individual progression risk.
- Existing Kidney Disease: Improving Global Outcomes (KDIGO) guidelines for adults are often applied to children, despite limited pediatric evidence.
Purpose of the Study:
- To evaluate the suitability of current KDIGO guidelines for treating IgAN in children.
- To highlight the need for pediatric-specific prediction models for IgAN progression.
- To advocate for personalized treatment strategies based on identified risk levels in pediatric IgAN.
Main Methods:
- Review of existing KDIGO guidelines and controversies conference statements.
- Analysis of the evidence base for IgAN treatment in pediatric populations.
- Discussion of the limitations of adult-based risk stratification in children.
Main Results:
- Current KDIGO guidelines are poorly adapted for treating IgAN in children due to scarce pediatric-specific evidence.
- Risk factors for progression in children may differ from adults, making adult schedules unsuitable.
- There is a significant gap in pediatric-focused prediction models for IgAN.
Conclusions:
- Pediatric IgAN management requires distinct approaches from adult guidelines.
- Development of novel prediction models is crucial for identifying children at risk of IgAN progression.
- Personalized treatment strategies, including targeted therapies, are needed for improved pediatric IgAN outcomes.
Abstract:
IgA nephropathy (IgAN) in children is no longer considered a rare and benign disease but a nephritis with different presentations and various outcomes. The decision to initiate a treatment and the therapeutic choice depend on the individual risk of progression. The Kidney Disease: Improving Global Outcomes (KDIGO) clinical guidelines in 2012 considered that the risk factors for progression of IgAN were similar in both children and adults and suggested in some conditions to follow the adult schedules. In 2017 a KDIGO Controversies Conference on management and treatment of glomerular diseases decided not to include an update in children with IgAN since the level of evidence of treatments in children was too scarce. Children can follow the indications for adults as far as the disease is similar in the various ages. This review is aimed at discussing why the KDIGO guidelines are poorly suitable to treat children with IgAN, and there is a need to develop new prediction models for progression of IgAN in children to guide selection of the cases to be treated. The identification of different risk levels in children with IgAN may personalize the choice of available drugs and support the use of new targeted therapies.
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