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. 2021 Apr;85(2):156-160.

Preliminary study of urinary excretion of liver-type fatty acid-binding protein in a cat model of chronic kidney disease

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Preliminary study of urinary excretion of liver-type fatty acid-binding protein in a cat model of chronic kidney disease

Akiko Watanabe et al. Can J Vet Res. 2021 Apr.

Abstract

Urinary liver-type fatty acid-binding protein (uL-FABP) is a clinically useful biomarker for monitoring chronic kidney disease (CKD) in humans. However, long-term monitoring of uL-FABP in CKD cats has not been reported. The objective of this preliminary study was to investigate whether the urinary excretion of L-FABP could predict the deterioration of renal function in 2 CKD model cats. Urinary liver-type fatty acid-binding protein (uL-FABP) increased before standard renal biomarkers, including serum creatinine, blood urea nitrogen, and symmetric dimethylarginine, in 1 cat with deteriorating renal function, but remained low and relatively stable in another cat with stable renal function. Our results suggest that uL-FABP is a potential clinical biomarker for predicting the progression of CKD in cats, as it is in humans.

La protéine urinaire de liaison aux acides gras de type hépatique (uL-FABP) est un biomarqueur cliniquement utile pour la surveillance de l’insuffisance rénale chronique (MRC) chez l’homme. Cependant, aucune surveillance à long terme de l’uL-FABP chez les chats atteints d’IRC n’a été signalée. L’objectif de cette étude préliminaire était de déterminer si l’excrétion urinaire de L-FABP pouvait prédire la détérioration de la fonction rénale chez deux chats modèles de CKD. La protéine uL-FABP a augmenté avant les biomarqueurs rénaux standards, y compris la créatinine sérique, l’azote uréique sanguin et la diméthylarginine symétrique, chez un chat dont la fonction rénale se détériorait, mais est restée faible et relativement stable chez un autre chat dont la fonction rénale était stable. Nos résultats suggèrent que l’uL-FABP est un biomarqueur clinique potentiel pour prédire la progression de l’IRC chez le chat, comme c’est le cas chez l’homme.(Traduit par Docteur Serge Messier).

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Figures

Figure 1
Figure 1
Time course of urinary liver-type fatty acid-binding protein (uL-FABP) and common renal function markers, including serum creatinine (sCre), blood urea nitrogen (BUN), and symmetric dimethylarginine (SDMA) in feline chronic kidney disease (CKD) models. A, C, E, and G — Cat 1. B, D, F, and H — Cat 2. The left ureter was ligated on day 0. The left ureter was released and anastomosed to the bladder mucosa on day 28. Right nephrectomy was conducted on day 42.
Figure 2
Figure 2
Histopathological images of Masson’s trichrome staining in CKD model cats. A — Right non-obstructed kidney tissues of Cat 2. B — Left obstructed kidney of Cat 1. Mild interstitial fibrosis, interstitial inflammation, and tubular atrophy were observed. C — Left obstructed kidney of Cat 2. Moderate interstitial fibrosis, interstitial inflammation, tubular dilation, and tubular atrophy were observed. Bar = 50 μm.

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