Epidemiology Research Unit, SAC (Scottish Agricultural College), King's Buildings, West Mains Road, Edinburgh EH9 3JG, UK.
Vet J. 2011 Jan;187(1):104-8. doi: 10.1016/j.tvjl.2009.10.024. Epub 2009 Nov 20.
Using a representative sample of Scottish sheep comprising 125 flocks, the sensitivity and specificity of PCR for Jaagsiekte sheep retrovirus (JSRV) was estimated. By combining and adapting existing methods, the characteristics of the diagnostic test were estimated (in the absence of a gold standard reference) using repeated laboratory replicates. As the results of replicates within the same animal cannot be considered to be independent, the performance of the PCR was calculated at individual replicate level. The median diagnostic specificity of the PCR when applied to individual animals drawn from the Scottish flock was estimated to be 0.997 (95% confidence interval [CI] 0.996-0.999), whereas the median sensitivity was 0.107 (95% CI 0.077-0.152). Considering the diagnostic test as three replicates where a positive result on any one or more replicates results in a positive test, the median sensitivity increased to 0.279. Reasons for the low observed sensitivity were explored by comparing the performance of the test as a function of the concentration of target DNA using spiked positive controls with known concentrations of target DNA. The median sensitivity of the test when used with positive samples with a mean concentration of 1.0 target DNA sequence per 25μL was estimated to be 0.160, which suggests that the PCR had a high true (analytical) sensitivity and that the low observed (diagnostic) sensitivity in individual samples was due to low concentrations of target DNA in the blood of clinically healthy animals.
利用包括 125 个羊群的苏格兰绵羊代表性样本,评估了聚合酶链反应(PCR)检测贾第虫绵羊反转录病毒(JSRV)的敏感性和特异性。通过结合和改编现有的方法,在缺乏金标准参考的情况下,利用实验室重复检测来估计诊断测试的特征(在同一只动物的重复结果不能被认为是独立的情况下)。由于同一动物内的重复结果不能被视为独立的,因此在个体重复水平上计算 PCR 的性能。当应用于从苏格兰羊群中抽取的个体动物时,PCR 的中位数诊断特异性估计为 0.997(95%置信区间 [CI] 0.996-0.999),而中位数敏感性为 0.107(95% CI 0.077-0.152)。考虑到诊断测试为三个重复,如果一个或多个重复的阳性结果导致阳性测试,则中位数敏感性增加到 0.279。通过使用具有已知目标 DNA 浓度的加标阳性对照物,比较测试作为目标 DNA 浓度函数的性能,探索了观察到的低敏感性的原因。当使用平均浓度为 25μL 中有 1.0 个目标 DNA 序列的阳性样本时,测试的中位数敏感性估计为 0.160,这表明 PCR 具有高的真实(分析)敏感性,并且在个体样本中观察到的低(诊断)敏感性是由于临床健康动物血液中目标 DNA 的浓度较低。