Wun Matthew K, Broughton-Neiswanger Liam E, Villarino Nicolas F
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Washington State University, Pullman, WA, United States.
Department of Veterinary Microbiology and Pathology, College of Veterinary Medicine, Washington State University, Pullman, WA, United States.
Front Vet Sci. 2024 May 15;11:1395505. doi: 10.3389/fvets.2024.1395505. eCollection 2024.
Serum symmetric dimethylarginine (SDMA) and creatinine are commonly used biomarkers of renal function in cats. We hypothesize that the serum analytes creatinine and SDMA are equally effective at detecting impaired renal function caused by meloxicam-induced renal injury in cats. Our primary objective was to compare serum concentrations of SDMA and creatinine in cats before, during, and after induction of renal injury from repeated dosages of meloxicam in the context of a small pilot study.
This follow-up study results from data collected in a well-controlled study that included 12 healthy female adult purpose-bred cats. Cats in the treatment group received meloxicam 0.3 mg/kg subcutaneously (SC) every 24 h for 31 days. Cats in the control group received saline (0.1 mL SC). Renal injury was defined as the presence of tubular damage, basement membrane damage, and/or interstitial inflammation in histological sections of kidney tissue. Serum creatinine and SDMA concentration were measured every 4 days.
In the control group, no cats developed renal azotemia. In the treatment group, four out of six cats developed elevated serum creatinine and histopathological evidence of renal injury. Three of these cats developed an elevation in serum SDMA. The time to the development of renal azotemia using serum creatinine or SDMA was not significantly different ( > 0.05).
In this pilot study, there was no evidence that serum SDMA was superior to serum creatinine at detecting impaired renal function caused by meloxicam-induced renal injury in cats.
血清对称二甲基精氨酸(SDMA)和肌酐是猫肾功能常用的生物标志物。我们假设血清分析物肌酐和SDMA在检测猫美洛昔康诱导的肾损伤所致肾功能损害方面同样有效。我们的主要目标是在一项小型试点研究的背景下,比较猫在重复给予美洛昔康诱导肾损伤之前、期间和之后血清中SDMA和肌酐的浓度。
这项随访研究的数据来自一项严格控制的研究,该研究纳入了12只健康的成年雌性专用猫。治疗组的猫每24小时皮下注射(SC)0.3mg/kg美洛昔康,持续31天。对照组的猫接受生理盐水(0.1mL SC)。肾损伤定义为肾组织组织学切片中存在肾小管损伤、基底膜损伤和/或间质炎症。每4天测量血清肌酐和SDMA浓度。
在对照组中,没有猫出现肾性氮血症。在治疗组中,6只猫中有4只出现血清肌酐升高和肾损伤的组织病理学证据。其中3只猫血清SDMA升高。使用血清肌酐或SDMA出现肾性氮血症的时间没有显著差异(>0.05)。
在这项试点研究中,没有证据表明血清SDMA在检测猫美洛昔康诱导的肾损伤所致肾功能损害方面优于血清肌酐。