Small sample adjustment for inference without assuming orthogonality in a mixed model for repeated measures analysis.

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY Journal of Biopharmaceutical Statistics Pub Date : 2024-10-29 DOI:10.1080/10543406.2024.2420632
Kazushi Maruo, Ryota Ishii, Yusuke Yamaguchi, Tomohiro Ohigashi, Masahiko Gosho
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Abstract

The mixed model for repeated measures (MMRM) analysis is sometimes used as a primary statistical analysis for a longitudinal randomized clinical trial. When the MMRM analysis is implemented in ordinary statistical software, the standard error of the treatment effect is estimated by assuming orthogonality between the fixed effects and covariance parameters, based on the characteristics of the normal distribution. However, orthogonality does not hold unless the normality assumption of the error distribution holds, and/or the missing data are derived from the missing completely at random structure. Therefore, assuming orthogonality in the MMRM analysis is not preferable. However, without the assumption of orthogonality, the small-sample bias in the standard error of the treatment effect is significant. Nonetheless, there is no method to improve small-sample performance. Furthermore, there is no software that can easily implement inferences on treatment effects without assuming orthogonality. Hence, we propose two small-sample adjustment methods inflating standard errors that are reasonable in ideal situations and achieve empirical conservatism even in general situations. We also provide an R package to implement these inference processes. The simulation results show that one of the proposed small-sample adjustment methods performs particularly well in terms of underestimation bias of standard errors; consequently, the proposed method is recommended. When using the MMRM analysis, our proposed method is recommended if the sample size is not large and between-group heteroscedasticity is expected.

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在重复测量分析的混合模型中,无需假定正交性即可进行推理的小样本调整。
重复测量混合模型(MMRM)分析有时被用作纵向随机临床试验的主要统计分析。在普通统计软件中实施 MMRM 分析时,会根据正态分布的特点,假设固定效应和协方差参数之间存在正交关系,从而估算治疗效果的标准误差。然而,除非误差分布的正态性假设成立,和/或缺失数据来自完全随机缺失结构,否则正交性不成立。因此,在 MMRM 分析中假设正交性并不可取。然而,如果不假设正交性,治疗效果标准误差的小样本偏差就会很大。然而,目前还没有改善小样本性能的方法。此外,也没有软件可以在不假设正交性的情况下轻松实现治疗效果的推断。因此,我们提出了两种夸大标准误差的小样本调整方法,这两种方法在理想情况下是合理的,即使在一般情况下也能实现经验保守性。我们还提供了一个 R 软件包来实现这些推理过程。模拟结果表明,其中一种建议的小样本调整方法在标准误差的低估偏差方面表现尤为突出;因此,建议使用该方法。在使用 MMRM 分析时,如果样本量不大且预计存在组间异方差,则推荐使用我们提出的方法。
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来源期刊
Journal of Biopharmaceutical Statistics
Journal of Biopharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.50
自引率
18.20%
发文量
71
审稿时长
6-12 weeks
期刊介绍: The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers: Drug, device, and biological research and development; Drug screening and drug design; Assessment of pharmacological activity; Pharmaceutical formulation and scale-up; Preclinical safety assessment; Bioavailability, bioequivalence, and pharmacokinetics; Phase, I, II, and III clinical development including complex innovative designs; Premarket approval assessment of clinical safety; Postmarketing surveillance; Big data and artificial intelligence and applications.
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