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Chronic kidney disease in children: an update
Luigi Cirillo1,2, Letizia De Chiara2, Samantha Innocenti1
1Nephrology and Dialysis Unit, Meyer Children's Hospital IRCCS, Florence, Italy.
Insights
Pediatric chronic kidney disease (CKD) is underdiagnosed due to challenges in definition. Advances in genetic sequencing suggest CKD is more common in children and adolescents than previously thought.
Area of Science:
- Nephrology
- Pediatric Nephrology
- Genetics
Background:
- Chronic kidney disease (CKD) is a significant global health concern.
- Accurate prevalence and consistent information on pediatric CKD are lacking.
- Current CKD definitions based on GFR and albuminuria are challenging in children due to age-related physiological changes, leading to underdiagnosis and delayed management.
Purpose of the Study:
- To review recent innovations in pediatric CKD.
- To provide a new perspective on CKD in children and adolescents.
- To highlight how advances in knowledge can improve diagnosis and management.
Main Methods:
- Review of recent literature on pediatric CKD.
- Focus on advances in understanding epidemiology and causes.
- Emphasis on the impact of massive-parallel sequencing technology.
Main Results:
- Massive-parallel sequencing has revised the understanding of CKD causes in children.
- Evidence suggests pediatric CKD is more frequent than currently reported.
- New knowledge is emerging on molecular pathways and cellular responses to kidney damage.
Conclusions:
- Advances in genetic technologies are crucial for a better understanding of pediatric CKD.
- Improved diagnostic criteria and management strategies are needed for children and adolescents.
- Future research will focus on identifying novel therapeutic targets for pediatric CKD.
Abstract:
Chronic kidney disease (CKD) is a major healthcare issue worldwide. However, the prevalence of pediatric CKD has never been systematically assessed and consistent information is lacking in this population. The current definition of CKD is based on glomerular filtration rate (GFR) and the extent of albuminuria. Given the physiological age-related modification of GFR in the first years of life, the definition of CKD is challenging per se in the pediatric population, resulting in high risk of underdiagnosis in this population, treatment delays and untailored clinical management. The advent and spreading of massive-parallel sequencing technology has prompted a profound revision of the epidemiology and the causes of CKD in children, supporting the hypothesis that CKD is much more frequent than currently reported in children and adolescents. This acquired knowledge will eventually converge in the identification of the molecular pathways and cellular response to damage, with new specific therapeutic targets to control disease progression and clinical features of children with CKD. In this review, we will focus on recent innovations in the field of pediatric CKD and in particular those where advances in knowledge have become available in the last years, with the aim of providing a new perspective on CKD in children and adolescents.
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