Higgins K M, Davidian M, Chew G, Burge H
CDER, Food and Drug Administration, Rockville, Maryland 20857, USA.
Biometrics. 1998 Mar;54(1):19-32.
A common practice in immunoassay is the use of sequential dilutions of an initial stock solution of the antigen of interest to obtain standard samples in a desired concentration range. Nonlinear, heteroscedastic regression models are a common framework for analysis, and the usual methods for fitting the model assume that measured responses on the standards are independent. However, the dilution procedure introduces a propagation of random measurement error that may invalidate this assumption. We demonstrate that failure to account for serial dilution error in calibration inference on unknown samples leads to serious inaccuracy of assessments of assay precision such as confidence intervals and precision profiles. Techniques for taking serial dilution error into account based on data from multiple assay runs are discussed and are shown to yield valid calibration inferences.
免疫测定中的一种常见做法是对感兴趣抗原的初始储备溶液进行连续稀释,以获得所需浓度范围内的标准样品。非线性、异方差回归模型是常见的分析框架,拟合该模型的常用方法假定标准品的测量响应是独立的。然而,稀释过程会引入随机测量误差的传播,这可能会使该假设无效。我们证明,在校准未知样品时若未考虑连续稀释误差,会导致诸如置信区间和精密度曲线等分析精密度评估出现严重不准确。本文讨论了基于多次测定运行数据考虑连续稀释误差的技术,并表明这些技术能产生有效的校准推断。