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Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is associated with concerning long-term implications for kidney function and cardiovascular health. Early intervention is needed in order to mitigate these long-term complications. Herein, we review...

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Autor principal: Cadnapaphornchai, Melissa A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362630/
https://www.ncbi.nlm.nih.gov/pubmed/28386535
http://dx.doi.org/10.3389/fped.2017.00053
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author Cadnapaphornchai, Melissa A.
author_facet Cadnapaphornchai, Melissa A.
author_sort Cadnapaphornchai, Melissa A.
collection PubMed
description Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is associated with concerning long-term implications for kidney function and cardiovascular health. Early intervention is needed in order to mitigate these long-term complications. Herein, we review important findings from recent clinical trials in ADPKD and their relevance to affected children and young adults and consider future directions for intervention. Recent clinical trials support aggressive control of blood pressure with blockade of the renin-angiotensin-aldosterone system as well as potential benefit of pravastatin therapy in children and young adults with ADPKD. There are several other candidate therapies, some of which have shown benefit in adult ADPKD, which require further investigation in affected children.
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spelling pubmed-53626302017-04-06 Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease Cadnapaphornchai, Melissa A. Front Pediatr Pediatrics Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is associated with concerning long-term implications for kidney function and cardiovascular health. Early intervention is needed in order to mitigate these long-term complications. Herein, we review important findings from recent clinical trials in ADPKD and their relevance to affected children and young adults and consider future directions for intervention. Recent clinical trials support aggressive control of blood pressure with blockade of the renin-angiotensin-aldosterone system as well as potential benefit of pravastatin therapy in children and young adults with ADPKD. There are several other candidate therapies, some of which have shown benefit in adult ADPKD, which require further investigation in affected children. Frontiers Media S.A. 2017-03-23 /pmc/articles/PMC5362630/ /pubmed/28386535 http://dx.doi.org/10.3389/fped.2017.00053 Text en Copyright © 2017 Cadnapaphornchai. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Cadnapaphornchai, Melissa A.
Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease
title Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease
title_full Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease
title_fullStr Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease
title_full_unstemmed Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease
title_short Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease
title_sort clinical trials in pediatric autosomal dominant polycystic kidney disease
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362630/
https://www.ncbi.nlm.nih.gov/pubmed/28386535
http://dx.doi.org/10.3389/fped.2017.00053
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