Polycystic Kidney Disease in Children: The Current Status and the Next Horizon
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, přehledy
Grantová podpora
R01 FD008225
FDA HHS - United States
K12 HD001399
NICHD NIH HHS - United States
U54 DK126087
NIDDK NIH HHS - United States
R03 DK127132
NIDDK NIH HHS - United States
R01 DK114425
NIDDK NIH HHS - United States
PubMed
40113156
PubMed Central
PMC12476570
DOI
10.1053/j.ajkd.2025.01.022
PII: S0272-6386(25)00772-3
Knihovny.cz E-zdroje
- Klíčová slova
- Childhood polycystic kidney disease, genetics, pediatric clinical trials, transition of care,
- MeSH
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- polycystické ledviny autozomálně dominantní * terapie diagnóza genetika MeSH
- polycystické ledviny autozomálně recesivní * terapie diagnóza genetika MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD) are inherited disorders that share many features such as kidney cysts, hypertension, urinary concentrating defects, and progressive chronic kidney disease. The underlying pathogenic mechanisms for both include cilia dysfunction and dysregulated intracellular signaling. ADPKD has been traditionally regarded as an adult-onset disease whereas ARPKD has been classically described as an infantile or childhood condition. However, clinicians must recognize that both disorders can present across all age groups, ranging from fetal life and infancy to childhood and adolescence as well as adulthood. Here we highlight the points of overlap and distinct features for these disorders with respect to pathogenesis, diagnostic modalities (radiological and genetic), clinical assessment, and early therapeutic management. In particular, we consider key issues at 2 critical points for transition of care: fetal life to infancy and adolescence to adulthood. These time points are poorly covered in the extant literature. Therefore, we recommend guiding principles for transitions of clinical care at these critical junctures in the life span. Although there is no cure for polycystic kidney disease (PKD), recent insights into pathogenic mechanisms have identified promising therapeutic targets that are currently being evaluated in a growing portfolio of clinical trials. We summarize the key findings from these largely adult-based trials and discuss the implications for designing child-focused studies. Finally, we look forward to the next horizon for childhood PKD, highlighting gaps in our current knowledge and discussing future directions and strategies to attenuate the full burden of disease for children affected with PKD.
Charles University Prague Czech Republic; Ostrava University Ostrava Czech Republic
Children's Hospital of Philadelphia and the University of Pennsylvania Philadelphia Pennsylvania
Children's National Hospital and the George Washington University Washington DC
Cleveland Clinic Children's Institute and Case Western Reserve University Cleveland Ohio
KU Leuven University and UZ Leuven Hospital Leuven Belgium
Townsville University Hospital and James Cook University Townsville Australia
University Children's Hospital Heidelberg Germany
University Hospital Cologne and the University of Cologne Cologne Germany
Zobrazit více v PubMed
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