Rosca Madalina, Forcada Yaiza, Solcan Gheorghe, Church David B, Niessen Stijn J M
1Department of Veterinary Clinical Sciences, 'Ion Ionescu de la Brad' University of Agricultural Sciences and Veterinary Medicine Iasi, Romania.
J Feline Med Surg. 2014 Feb;16(2):82-8. doi: 10.1177/1098612X13496246. Epub 2013 Jul 4.
Screening diabetic cats for feline hypersomatotropism (HS) is currently dependent on using a radioimmunoassay (RIA) for measurement of growth hormone or insulin-like growth factor 1 (IGF-1), both of which require radioactivity, are costly and have limited availability. Performance of an enzyme-linked immunosorbent assay (ELISA) using anti-human IGF-1 antibodies was assessed. Total IGF-1 was determined in diabetic cat samples across a wide range of IGF-concentrations using a previously validated RIA (serum: 92 cats; plasma: 31 cats). Repeat IGF-1 measurement was then performed using the ELISA-system. Mean IGF-1 recovery after serial dilution proved satisfactory with a correlation coefficient of 0.96 (serum) and 0.97 (plasma). Appropriate precision was established [intra-assay coefficient of variation (CV) 9.5 ± 2% (serum) and 13.6 ± 7% (plasma); inter-assay CV 11.4 ± 4% (serum) and 7.6 ± 6% (plasma)] and significant effect of hyperlipidaemia, haemoglobinaemia, bilirubinaemia and storage was excluded, with the exception of an increase in serum IGF-1 when left at room temperature for more than 24 h. ELISA concentrations correlated significantly with RIA concentrations (serum Pearson r(2): 0.75; plasma: 0.83, P <0.001). Receiver operating characteristics analysis showed an area under the curve of 0.99 (serum) and 0.96 (plasma), and indicated high diagnostic accuracy for categorising a diabetic cat correctly as suspicious for HS at a serum IGF-1 cut-off of 997 ng/ml (sensitivity, 100%; specificity, 88.1%). The current study is the first to validate an easy-to-use and economical IGF-1 ELISA for the screening for HS among diabetic cats, which is important given the suspected significant prevalence of HS-induced diabetes mellitus.
目前,筛查患有猫垂体生长激素分泌亢进症(HS)的糖尿病猫依赖于使用放射免疫分析法(RIA)来测量生长激素或胰岛素样生长因子1(IGF-1),这两种方法都需要放射性物质,成本高昂且可用性有限。评估了使用抗人IGF-1抗体的酶联免疫吸附测定法(ELISA)的性能。使用先前验证的RIA在广泛的IGF浓度范围内测定糖尿病猫样本中的总IGF-1(血清:92只猫;血浆:31只猫)。然后使用ELISA系统进行IGF-1的重复测量。系列稀释后的平均IGF-1回收率令人满意,血清的相关系数为0.96,血浆的相关系数为0.97。确定了适当的精密度[批内变异系数(CV),血清为9.5±2%,血浆为13.6±7%;批间CV,血清为11.4±4%,血浆为7.6±6%],排除了高脂血症、血红蛋白血症、胆红素血症和样本储存的显著影响,但血清IGF-1在室温下放置超过24小时会增加。ELISA浓度与RIA浓度显著相关(血清Pearson r²:0.75;血浆:0.83,P<0.001)。受试者工作特征分析显示,血清曲线下面积为0.99,血浆为0.96,表明在血清IGF-1临界值为997 ng/ml时,将糖尿病猫正确分类为疑似HS具有很高的诊断准确性(敏感性为100%;特异性为88.1%)。本研究首次验证了一种易于使用且经济的IGF-1 ELISA用于筛查糖尿病猫中的HS,鉴于疑似HS诱导的糖尿病患病率较高,这一点很重要。