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Related Experiment Video

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Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
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[New therapies for ADPKD].

M Rathaus1

  • 1Unità di Emodialisi, Dipartimento di Nefrologia e Ipertensione, Meir Medical Center, Kfar Saba and Sackler School of Medicine, Tel Aviv University, Kfar Saba, Israel. maurorat@clalit.org.il

Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia
|February 19, 2008
PubMed
Summary

Autosomal dominant polycystic kidney disease (ADPKD) is a leading cause of kidney failure with no current specific treatments. Research is advancing understanding and developing novel therapies to slow disease progression and shift treatment from passive to active management.

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Implementing Patch Clamp and Live Fluorescence Microscopy to Monitor Functional Properties of Freshly Isolated PKD Epithelium
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Implementing Patch Clamp and Live Fluorescence Microscopy to Monitor Functional Properties of Freshly Isolated PKD Epithelium
08:46

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Published on: September 1, 2015

Area of Science:

  • Nephrology
  • Genetics
  • Pharmacology

Context:

  • Autosomal dominant polycystic kidney disease (ADPKD) is a prevalent genetic disorder and a major cause of end-stage renal disease.
  • Current management focuses on supportive care and managing complications, lacking disease-specific interventions to halt progression.

Purpose:

  • To review current therapeutic strategies and novel approaches for managing ADPKD.
  • To highlight recent advancements in understanding ADPKD pathogenesis and their translation into potential treatments.

Summary:

  • ADPKD treatment options are evolving, with established therapies including dietary modifications and medications like ACE inhibitors/ARBs and statins.
  • Novel therapeutic strategies target cyst epithelium proliferation (e.g., C-myc oligonucleotides, kinase inhibitors) and cyst fluid secretion (e.g., vasopressin V2 receptor antagonists).
  • While some novel treatments are in clinical trials, the future of ADPKD management likely involves combination therapies targeting diverse pathogenetic mechanisms.

Impact:

  • This review anticipates a paradigm shift in ADPKD care towards proactive, multifaceted treatment protocols.
  • Advancements promise to significantly improve patient prognosis and quality of life by actively managing disease progression.