Antenatal biological models in the characterization and research of congenital lower urinary tract disorders

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisReviewForskningpeer review

  • Kevin Xi Cao, University College London, Great Ormond Street Hospital for Children NHS Foundation Trust
  • ,
  • Nathalie Jane Milmoe, University College London
  • ,
  • Peter Malcom Cuckow, Great Ormond Street Hospital for Children NHS Foundation Trust
  • ,
  • Lars Henning Olsen
  • Navroop Singh Johal, Aarhus Universitet
  • ,
  • Paul Julian Douglas Winyard, University College London
  • ,
  • David Andrew Long, University College London
  • ,
  • Christopher Henry Fry, University of Bristol

Congenital lower urinary tract disorders are a family of diseases affecting both urinary storage and voiding as well as upstream kidney function. Current treatments include surgical reconstruction but many children still fail to achieve urethral continence or progress to chronic kidney disease. New therapies can only be achieved through undertaking research studies to enhance our understanding of congenital lower urinary tract disorders. Animal models form a critical component of this research, a corner of the triangle composed of human in-vitro studies and clinical research. We describe the current animal models for two rare congenital bladder disorders, posterior urethral valves (PUV) and bladder exstrophy (BE). We highlight important areas for researchers to consider when deciding which animal model to use to address particular research questions and outline the strengths and weaknesses of current models available for PUV and BE. Finally, we present ideas for refining animal models for PUV and BE in the future to stimulate future researchers and help them formulate their thinking when working in this field.

OriginalsprogEngelsk
TidsskriftJournal of Pediatric Urology
Vol/bind17
Nummer1
Sider (fra-til)21-29
Antal sider9
ISSN1477-5131
DOI
StatusUdgivet - feb. 2021

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