四种不同精度分布的回归框架在模拟参考物质可交换性评估中的性能

C. Markus, Rui Zhen Tan, Chun Yee Lim, W. Rankin, S. Matthews, T. P. Loh, W. Hague
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引用次数: 1

摘要

摘要目的评估参考物质(RM)可交换性及其与临床样本(CS)一致性的一种方法是使用带预测区间的普通最小二乘或戴明回归。这种方法假设恒定的方差,这可能无法通过测量过程实现。灵活的回归框架放宽了这一假设,如分位数回归或广义的位置、规模和形状加性模型(GAMLSS),最近已经实现,它可以模拟随测量浓度变化的方差。方法模拟了从简单的恒定方差到复杂的恒定和比例混合方差的4种不精确剖面,研究了上述4种回归框架以及不同的CS数量、数据转换和RM相对于CS浓度的位置对可交换性评估结果的影响。回归框架的性能由预测区间或相对RM浓度的可交换性错误拒绝的比例决定,并与预期的名义概率覆盖率进行比较。结果在简单方差曲线(常数或比例方差)中,Deming回归、不加对数变换和加对数变换是最有效的方法。在混合方差曲线中,考虑到增加CS的数量和RM的相对位置,采用平滑技术的GAMLSS更为合适。在变异曲线的分析系数为u形的情况下,即使是更灵活的回归框架也可能不完全合适。结论在可交换性评估中,测量方法和RM位置相对于临床样品浓度的方差分布显著影响可交换性的错误拒绝率。
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Performance of four regression frameworks with varying precision profiles in simulated reference material commutability assessment
Abstract Objectives One approach to assessing reference material (RM) commutability and agreement with clinical samples (CS) is to use ordinary least squares or Deming regression with prediction intervals. This approach assumes constant variance that may not be fulfilled by the measurement procedures. Flexible regression frameworks which relax this assumption, such as quantile regression or generalized additive models for location, scale, and shape (GAMLSS), have recently been implemented, which can model the changing variance with measurand concentration. Methods We simulated four imprecision profiles, ranging from simple constant variance to complex mixtures of constant and proportional variance, and examined the effects on commutability assessment outcomes with above four regression frameworks and varying the number of CS, data transformations and RM location relative to CS concentration. Regression framework performance was determined by the proportion of false rejections of commutability from prediction intervals or centiles across relative RM concentrations and was compared with the expected nominal probability coverage. Results In simple variance profiles (constant or proportional variance), Deming regression, without or with logarithmic transformation respectively, is the most efficient approach. In mixed variance profiles, GAMLSS with smoothing techniques are more appropriate, with consideration given to increasing the number of CS and the relative location of RM. In the case where analytical coefficients of variation profiles are U-shaped, even the more flexible regression frameworks may not be entirely suitable. Conclusions In commutability assessments, variance profiles of measurement procedures and location of RM in respect to clinical sample concentration significantly influence the false rejection rate of commutability.
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