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首页> 外文期刊>Veterinary Research Communications >Evaluation of a Commercially Available Human Serum Amyloid A (SAA) Turbidimetric Immunoassay for Determination of Feline SAA Concentration
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Evaluation of a Commercially Available Human Serum Amyloid A (SAA) Turbidimetric Immunoassay for Determination of Feline SAA Concentration

机译:评价用于测定猫SAA浓度的市售人血清淀粉样蛋白A(SAA)浊度免疫法

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摘要

Serum amyloid A (SAA) is an acute-phase protein in cats likely to be useful for diagnosing and monitoring inflammatory diseases, especially if rapid, reliable and automated assays can be made available. A commercially available automated human SAA turbidimetric immunoassay (SAA-TIA) was evaluated for determination of SAA in cats. Intra-assay and inter-assay imprecisions were in the ranges 2.1–9.9% and 7.0–12.5%, respectively, and without significant inaccuracy. Eighty-eight cats were divided into groups according to (A) the presence or absence of an acute-phase response (APR) (n = 23 and 65, respectively) and (B) clinical diagnosis (clinically healthy cats, cats diagnosed with inflammatory/infectious diseases, endocrine/metabolic diseases, neoplastic diseases, and miscellaneous disorders (n=43, 13, 8, 4 and 20, respectively)). The observed SAA concentrations were, as expected, different for (A) cats with and without an APR and (B) cats with inflammatory/infectious diseases compared to other diagnostic groups, except neoplastic diseases. In conclusion, the SAA concentration in cats could be measured reliably using the commercially available TIA designed for measuring human SAA, which should facilitate implementation of the parameter for routine diagnostic purposes.
机译:血清淀粉样蛋白A(SAA)是猫的一种急性期蛋白,可能可用于诊断和监测炎症性疾病,尤其是如果可以提供快速,可靠和自动化的测定方法时。评价了市售的自动化人SAA比浊免疫分析(SAA-TIA),以确定猫中的SAA。批内和批间不准确度分别在2.1%至9.9%和7.0%至12.5%之间,并且没有明显的误差。根据(A)是否存在急性期反应(APR)(分别为n = 23和65)和(B)临床诊断(临床健康的猫,被诊断为发炎的猫)将88只猫分为几组/传染病,内分泌/代谢疾病,赘生性疾病和其他疾病(分别为n = 43、13、8、4和20)。与预期的相比,除了赘生性疾病外,与其他诊断组相比,(A)有和没有APR的猫和(B)有炎性/传染病的猫的观察到的SAA浓度是不同的。总之,可以使用设计用于测量人SAA的市售TIA可靠地测量猫中SAA的浓度,这应该有助于常规诊断目的参数的实现。

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