Urinary liver-type fatty acid-binding protein in clinically healthy elderly cats: Evaluation of its potential to detect IRIS stage 1 chronic kidney disease and borderline proteinuria

被引:2
|
作者
Kongtasai, Thirawut [1 ,2 ,5 ]
Paepe, Dominique [1 ]
Mortier, Femke [1 ]
Marynissen, Sofie
Meyer, Evelyne [3 ]
Duchateau, Luc [4 ]
Daminet, Sylvie [1 ]
机构
[1] Univ Ghent, Fac Vet Med, Small Anim Dept, Merelbeke, Belgium
[2] Mahidol Univ, Fac Vet Med, Dept Clin Sci & Publ Hlth, Nakhon Pathom, Thailand
[3] Univ Ghent, Fac Vet Med, Dept Pharmacol, Toxicol & Biochem, Merelbeke, Belgium
[4] Univ Ghent, Fac Vet Med, Dept Nutr, Genet & Ethol, Merelbeke, Belgium
[5] Univ Ghent, Fac Vet Med, SmallAnimal Dept, Salisburylaan133, B-9820 Merelbeke, Belgium
关键词
renal biomarker; aged cats; screening; feline CKD; L-FABP; GLOMERULAR-FILTRATION-RATE; L-FABP; BIOMARKERS; MARKERS; CREATININE; EXCRETION; DIAGNOSIS; INJURY; ESRD;
D O I
10.1002/vms3.1003
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
BackgroundUrinary liver-type fatty acid-binding protein (uL-FABP) is a promising biomarker to detect early chronic kidney disease (CKD) in cats. Few healthy cats show increased uL-FABP for unknown reasons. ObjectivesThe objective of this study was to evaluate uL-FABP in a large healthy elderly cat population comparing cats with and without International Renal Interest Society (IRIS) stage 1 CKD and with and without borderline proteinuria. MethodsThis was a cross-sectional study. One hundred ninety-six clinically healthy client-owned cats of >= 7 years old were subdivided based on two criteria: (1) having either IRIS stage 1 CKD or no evidence of CKD and (2) having borderline proteinuria or no proteinuria. Urinary L-FABP was measured using a validated commercially available feline L-FABP ELISA. ResultsOverall, uL-FABP was detectable in 6/196 (3%) healthy elderly cats. For the first subdivision, nine (5%) cats had IRIS stage 1 CKD, 184 cats had no evidence CKD and three cats were excluded. All cats with IRIS stage 1 CKD had uL-FABP concentrations below the detection limit, whereas 6/184 (3%) cats without IRIS stage 1 CKD had detectable uL-FABP concentrations (median 1.79 ng/ml, range 0.79-3.66 ng/ml). For the second subdivision, 47 (24%) cats had borderline proteinuria, 147 cats had no proteinuria and two cats were excluded. One of the borderline proteinuric cats had a detectable uL-FABP concentration, whereas the other five cats with detectable uL-FABP concentrations were non-proteinuric. ConclusionWith the current assay, the screening potential of uL-FABP as an early biomarker for feline CKD is limited as uL-FABP was rarely detected in clinically healthy elderly cats independently of the presence of either IRIS stage 1 CKD or borderline proteinuria.
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收藏
页码:3 / 12
页数:10
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