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The cardiovascular effect of the uremic solute indole-3 acetic acid.

Abstract
In CKD, uremic solutes may induce endothelial dysfunction, inflammation, and oxidative stress, leading to increased cardiovascular risk. We investigated whether the uremic solute indole-3 acetic acid (IAA) predicts clinical outcomes in patients with CKD and has prooxidant and proinflammatory effects. We studied 120 patients with CKD. During the median study period of 966 days, 29 patients died and 35 experienced a major cardiovascular event. Kaplan-Meier analysis revealed that mortality and cardiovascular events were significantly higher in the higher IAA group (IAA>3.73 µM) than in the lower IAA group (IAA<3.73 µM). Multivariate Cox regression analysis demonstrated that serum IAA was a significant predictor of mortality and cardiovascular events after adjustments for age and sex; cholesterol, systolic BP, and smoking; C-reactive protein, phosphate, body mass index, and albumin; diastolic BP and history of cardiovascular disease; and uremic toxins p-cresyl sulfate and indoxyl sulfate. Notably, IAA level remained predictive of mortality when adjusted for CKD stage. IAA levels were positively correlated with markers of inflammation and oxidative stress: C-reactive protein and malondialdehyde, respectively. In cultured human endothelial cells, IAA activated an inflammatory nongenomic aryl hydrocarbon receptor (AhR)/p38MAPK/NF-κB pathway that induced the proinflammatory enzyme cyclooxygenase-2. Additionally, IAA increased production of endothelial reactive oxygen species. In conclusion, serum IAA may be an independent predictor of mortality and cardiovascular events in patients with CKD. In vitro, IAA induces endothelial inflammation and oxidative stress and activates an inflammatory AhR/p38MAPK/NF-κB pathway.
AuthorsLaetitia Dou, Marion Sallée, Claire Cerini, Stéphane Poitevin, Bertrand Gondouin, Noemie Jourde-Chiche, Karim Fallague, Philippe Brunet, Raymond Calaf, Bertrand Dussol, Bernard Mallet, Françoise Dignat-George, Stephane Burtey
JournalJournal of the American Society of Nephrology : JASN (J Am Soc Nephrol) Vol. 26 Issue 4 Pg. 876-87 (Apr 2015) ISSN: 1533-3450 [Electronic] United States
PMID25145928 (Publication Type: Journal Article)
CopyrightCopyright © 2015 by the American Society of Nephrology.
Chemical References
  • Indoleacetic Acids
  • Reactive Oxygen Species
  • indoleacetic acid
  • Cyclooxygenase 2
  • PTGS2 protein, human
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Cardiovascular Diseases (blood, etiology)
  • Cyclooxygenase 2 (metabolism)
  • Endothelium, Vascular (metabolism)
  • Female
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Indoleacetic Acids (blood)
  • Male
  • Middle Aged
  • Oxidative Stress
  • Reactive Oxygen Species (metabolism)
  • Renal Insufficiency, Chronic (blood, complications, mortality)
  • Signal Transduction
  • Uremia (complications)
  • Young Adult

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