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Cardiovascular Polycystins: Insights From Autosomal Dominant Polycystic Kidney Disease and Transgenic Animal Models

Authors :
Delphine Bichet
Patrick Delmas
Amanda Patel
Eric Honoré
Dorien Peters
Institut de pharmacologie moléculaire et cellulaire (IPMC)
Université Nice Sophia Antipolis (... - 2019) (UNS)
COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS)
Laboratoire de neurophysiologie cellulaire (LNPC)
Université de la Méditerranée - Aix-Marseille 2-Centre National de la Recherche Scientifique (CNRS)
Université Nice Sophia Antipolis (1965 - 2019) (UNS)
Source :
Trends in Cardiovascular Medicine, Trends in Cardiovascular Medicine, Elsevier, 2006, 16 (8), pp.292-298, HAL, Trends in Cardiovascular Medicine, 2006, 16 (8), pp.292-298
Publication Year :
2006
Publisher :
HAL CCSD, 2006.

Abstract

Mutations in the PKD1 and PKD2 polycystin genes are responsible for autosomal dominant polycystic kidney disease (ADPKD), one of the most prevalent genetic kidney disorders. ADPKD is a multisystem disease characterized by the formation of numerous fluid-filled cysts in the kidneys, the pancreas, and the liver. Moreover, major cardiovascular manifestations are common complications in ADPKD. Intracranial aneurysms and arterial hypertension are among the leading causes of mortality in this disease. In the present review, we summarize our current understanding of the role of polycystins in the development, maintenance, and function of the cardiovascular system.

Details

Language :
English
ISSN :
10501738
Database :
OpenAIRE
Journal :
Trends in Cardiovascular Medicine, Trends in Cardiovascular Medicine, Elsevier, 2006, 16 (8), pp.292-298, HAL, Trends in Cardiovascular Medicine, 2006, 16 (8), pp.292-298
Accession number :
edsair.doi.dedup.....b18580d27d7ee2fc8ecd6a268421a26e