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Pravastatin Therapy and Biomarker Changes in Children and Young Adults with Autosomal Dominant Polycystic Kidney Disease.
- Source :
-
Clinical journal of the American Society of Nephrology : CJASN [Clin J Am Soc Nephrol] 2015 Sep 04; Vol. 10 (9), pp. 1534-41. Date of Electronic Publication: 2015 Jul 29. - Publication Year :
- 2015
-
Abstract
- Background and Objectives: Disease-specific treatment options for autosomal dominant polycystic kidney disease are limited. Clinical intervention early in life is likely to have the greatest effect. In a 3-year randomized double-blind placebo-controlled phase 3 clinical trial, the authors recently showed that pravastatin decreased height-corrected total kidney volume (HtTKV) progression of structural kidney disease over a 3-year period. However, the underlying mechanisms have not been elucidated.<br />Design, Setting, Participants, & Measurements: Participants were recruited nationally from July 2007 through October 2009. Plasma and urine samples collected at baseline, 18 months, and 36 months from 91 pediatric patients enrolled in the above-mentioned clinical trial were subjected to mass spectrometry-based biomarker analysis. Changes in biomarkers over 3 years were compared between placebo and pravastatin-treated groups. Linear regression was used to evaluate the changes in biomarkers with the percent change in HtTKV over 3 years.<br />Results: Changes in plasma concentrations of proinflammatory and oxidative stress markers (9- hydroxyoctadecadienoic acid, 13-hydroxyoctadecadienoic acid, and 15-hydroxyeicosatetraenoic acid [HETE]) over 3 years were significantly different between the placebo and pravastatin-treated groups, with the pravastatin group showing a lower rate of biomarker increase. Urinary 8-HETE, 9-HETE, and 11-HETE were positively associated with the changes in HtTKV in the pravastatin group.<br />Conclusions: Pravastatin therapy diminished the increase of cyclooxygenase- and lipoxygenase-derived plasma lipid mediators. The identified biomarkers and related molecular pathways of inflammation and endothelial dysfunction may present potential targets for monitoring of disease severity and therapeutic intervention of autosomal dominant polycystic kidney disease.<br /> (Copyright © 2015 by the American Society of Nephrology.)
- Subjects :
- 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid blood
Adolescent
Biomarkers blood
Biomarkers urine
Child
Female
Humans
Hydroxyeicosatetraenoic Acids blood
Hydroxyeicosatetraenoic Acids urine
Linoleic Acids blood
Male
Organ Size drug effects
Oxidative Stress
Polycystic Kidney, Autosomal Dominant drug therapy
Time Factors
Young Adult
Hydroxymethylglutaryl-CoA Reductase Inhibitors therapeutic use
Polycystic Kidney, Autosomal Dominant blood
Polycystic Kidney, Autosomal Dominant urine
Pravastatin therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1555-905X
- Volume :
- 10
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Clinical journal of the American Society of Nephrology : CJASN
- Publication Type :
- Academic Journal
- Accession number :
- 26224879
- Full Text :
- https://doi.org/10.2215/CJN.11331114