期刊
RESEARCH IN VETERINARY SCIENCE
卷 135, 期 -, 页码 547-554出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.rvsc.2020.11.005
关键词
Acute kidney injury; Biomarkers; Dogs; ELISA; Multiplex immunoassays
资金
- Australian Companion Animal Health Foundation Research Grant [011/2015]
This study compared the use of two different multiplex assays and previously-validated single analyte immunoassays for measuring five biomarkers in canine samples during ischaemia-reperfusion (IR) acute kidney injury. Only NGAL showed significant elevation following IR, while the concentrations of the other four biomarkers varied depending on the assay used. The concentrations of cystatin C and KIM-1 measured with multiplex assays were much lower compared to single analyte ELISAs, indicating the need for further validation before reliable use in measuring AKI biomarkers in canine samples.
Several protein biomarkers have been shown to be useful for the early diagnosis of acute kidney injury (AKI) in animals and people. Multiplex assays for measurement of a panel of renal biomarkers in canine samples have recently become available. This study compared the use of two such assays, versus previously validated ELISAs, to measure five biomarkers in canine samples during ischaemia-reperfusion (IR) AKI. Blood and urine was collected from six male anaesthetised greyhounds that underwent 1-h of renal ischaemia (severe hypotension induced by acute haemorrhage) and 2-h of reperfusion (intravenous fluid resuscitation). Histology confirmed presence of acute tubular injury at 2 h of reperfusion. Concentrations of clusterin, cystatin C, kidney-injury molecule 1 (KIM-1), monocyte chemoattractant protein 1, and neutrophil gelatinase-associated lipocalin (NGAL) at baseline and following IR, measured by two different multiplex assays and previously-validated single analyte immunoassays, were compared. Only NGAL was significantly elevated following IR with all assays investigated. Whether concentrations of the other four biomarkers were significantly increased following IR depended on the assay used. Concentrations of cystatin C and KIM-1 measured with the multiplex assays were of a vast magnitude lower than those measured with the corresponding single analyte ELISAs. We conclude that further validation is required before these assays can reliably be used to measure AKI biomarkers in canine samples.
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