Enhanced MCP-1 Release in Early Autosomal Dominant Polycystic Kidney Disease

Enhanced MCP-1 Release in Early Autosomal Dominant Polycystic Kidney Disease

Introduction: Autosomal dominant polycystic kidney disease (ADPKD) causes kidney failure typically in adulthood, but the disease starts in utero. Copeptin, epidermal growth factor (EGF), and monocyte chemoattractant protein-1 (MCP-1) are associated with severity and hold prognostic value in adults b...

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Bibliographic Details
Main Authors: Peter Janssens, Jean-Paul Decuypere, Stéphanie De Rechter, Luc Breysem, Dorien Van Giel, Jaak Billen, An Hindryckx, Luc De Catte, Marcella Baldewijns, Kathleen B.M. Claes, Karl M. Wissing, Koen Devriendt, Bert Bammens, Isabelle Meyts, Vicente E. Torres, Rudi Vennekens, Djalila Mekahli
Format: Article
Language:English
Published: Elsevier 2021-06-01
Series:Kidney International Reports
Subjects:
ADPKD
chemokine
distal tubule
inflammation
pediatric nephrology
proximal tubule
Online Access:http://www.sciencedirect.com/science/article/pii/S246802492101041X

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http://www.sciencedirect.com/science/article/pii/S246802492101041X

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