Evaluation of oxidative stress in dogs and cats with chronic kidney disease

Abstract Background Oxidative stress is a potential contributor to chronic kidney disease (CKD) progression but has not been evaluated in dogs and cats with CKD. Hypothesis Oxidative stress is higher in animals with CKD compared with healthy controls and decreases with the advancing CKD stage. The a...

Full description

Saved in:
Bibliographic Details
Main Authors: Hilla Chen, Gilad Segev
Format: Article
Language:English
Published: Wiley 2024-11-01
Series:Journal of Veterinary Internal Medicine
Subjects:
Online Access:https://doi.org/10.1111/jvim.17230
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850159105005584384
author Hilla Chen
Gilad Segev
author_facet Hilla Chen
Gilad Segev
author_sort Hilla Chen
collection DOAJ
description Abstract Background Oxidative stress is a potential contributor to chronic kidney disease (CKD) progression but has not been evaluated in dogs and cats with CKD. Hypothesis Oxidative stress is higher in animals with CKD compared with healthy controls and decreases with the advancing CKD stage. The aim of this study was to determine the presence and intensity of oxidative stress in dogs and cats at different CKD stages. Animals Sixty dogs and 30 cats with naturally acquired CKD; 10 dogs and 14 cats, healthy controls. Methods Analytical cross‐sectional study. Oxidative stress was evaluated by measuring the urinary concentration of F2‐isoprostane (uF2‐IsoPs) normalized to urinary creatinine. Results Urinary F2‐isoprostanes normalized to urinary creatinine of healthy dogs and of dogs with CKD Stages 1 to 4 was 3.3 ng/mg, 4.7 ng/mg (range, 1.0‐73.4), 2.4 ng/mg (range, 0.4‐7.8), 0.52 ng/mg (range, 0.01‐2.9), and 0.37 ng/mg (range, 0.01‐0.6), respectively. Urinary F2‐isoprostanes differed among CKD stages (P < .001), but not compared with controls. uF2‐IsoPs of healthy cats and cats with CKD Stages 1 to 4 was 0.68 ng/mg (range, 0.2‐1.4), 0.97 ng/mg (range, 0.4‐1.8), 0.6 ng/mg (range, 0.002‐2.0), 0.94 ng/mg (range, 0.3‐2.3), and 0.2 ng/mg (range, 0.01‐0.4). Urinary F2‐isoprostanes differed among stages (P = .05) but not compared with healthy controls. Conclusion and Clinical Importance Oxidative stress might be present in dogs and cats with CKD. Its magnitude declines as the disease progresses, therefore, it should be considered a potential therapeutic target mostly at the early stages of the disease.
format Article
id doaj-art-3e855e0da54e43c19be2035d7189539f
institution OA Journals
issn 0891-6640
1939-1676
language English
publishDate 2024-11-01
publisher Wiley
record_format Article
series Journal of Veterinary Internal Medicine
spelling doaj-art-3e855e0da54e43c19be2035d7189539f2025-08-20T02:23:40ZengWileyJournal of Veterinary Internal Medicine0891-66401939-16762024-11-013863105311010.1111/jvim.17230Evaluation of oxidative stress in dogs and cats with chronic kidney diseaseHilla Chen0Gilad Segev1Department of Small Animal Internal Medicine Koret School of Veterinary Medicine, The Hebrew University of Jerusalem Rehovot IsraelDepartment of Small Animal Internal Medicine Koret School of Veterinary Medicine, The Hebrew University of Jerusalem Rehovot IsraelAbstract Background Oxidative stress is a potential contributor to chronic kidney disease (CKD) progression but has not been evaluated in dogs and cats with CKD. Hypothesis Oxidative stress is higher in animals with CKD compared with healthy controls and decreases with the advancing CKD stage. The aim of this study was to determine the presence and intensity of oxidative stress in dogs and cats at different CKD stages. Animals Sixty dogs and 30 cats with naturally acquired CKD; 10 dogs and 14 cats, healthy controls. Methods Analytical cross‐sectional study. Oxidative stress was evaluated by measuring the urinary concentration of F2‐isoprostane (uF2‐IsoPs) normalized to urinary creatinine. Results Urinary F2‐isoprostanes normalized to urinary creatinine of healthy dogs and of dogs with CKD Stages 1 to 4 was 3.3 ng/mg, 4.7 ng/mg (range, 1.0‐73.4), 2.4 ng/mg (range, 0.4‐7.8), 0.52 ng/mg (range, 0.01‐2.9), and 0.37 ng/mg (range, 0.01‐0.6), respectively. Urinary F2‐isoprostanes differed among CKD stages (P < .001), but not compared with controls. uF2‐IsoPs of healthy cats and cats with CKD Stages 1 to 4 was 0.68 ng/mg (range, 0.2‐1.4), 0.97 ng/mg (range, 0.4‐1.8), 0.6 ng/mg (range, 0.002‐2.0), 0.94 ng/mg (range, 0.3‐2.3), and 0.2 ng/mg (range, 0.01‐0.4). Urinary F2‐isoprostanes differed among stages (P = .05) but not compared with healthy controls. Conclusion and Clinical Importance Oxidative stress might be present in dogs and cats with CKD. Its magnitude declines as the disease progresses, therefore, it should be considered a potential therapeutic target mostly at the early stages of the disease.https://doi.org/10.1111/jvim.17230biomarkersCKD progressionF2‐isprostanesproteinuriarenal diet
spellingShingle Hilla Chen
Gilad Segev
Evaluation of oxidative stress in dogs and cats with chronic kidney disease
Journal of Veterinary Internal Medicine
biomarkers
CKD progression
F2‐isprostanes
proteinuria
renal diet
title Evaluation of oxidative stress in dogs and cats with chronic kidney disease
title_full Evaluation of oxidative stress in dogs and cats with chronic kidney disease
title_fullStr Evaluation of oxidative stress in dogs and cats with chronic kidney disease
title_full_unstemmed Evaluation of oxidative stress in dogs and cats with chronic kidney disease
title_short Evaluation of oxidative stress in dogs and cats with chronic kidney disease
title_sort evaluation of oxidative stress in dogs and cats with chronic kidney disease
topic biomarkers
CKD progression
F2‐isprostanes
proteinuria
renal diet
url https://doi.org/10.1111/jvim.17230
work_keys_str_mv AT hillachen evaluationofoxidativestressindogsandcatswithchronickidneydisease
AT giladsegev evaluationofoxidativestressindogsandcatswithchronickidneydisease