在生物医学研究中同时推断多个二进制终点:多个边际模型的小样本属性和重新采样方法
Sören Budig1, Klaus Jung2, Mario Hasler3
1Department of Biostatistics, Institute of Cell Biology and Biophysics, Leibniz University Hannover, Hannover, Germany.
Biometrical journal. Biometrische Zeitschrift
|July 2, 2024
概括
本研究比较了生物医学研究中分析多个二进制结果的方法. 再抽样方法提供了更好的统计能力,同时控制错误,优于多个边际模型和邦费罗尼校正.
科学领域:
- 生物统计学 生物统计学
- 生物医学研究方法学
背景情况:
- 对多个二进制终点的同时推断在生物医学研究中至关重要.
- 控制家庭智能错误率 (FWER) 对于避免错误的测试决策至关重要.
研究的目的:
- 调查和比较单步 p 值调整方法,以考虑终点相关性.
- 评估多个边缘模型的性能和基于矢量的重新采样方法与Bonferroni方法对比.
主要方法:
- 研究了单步 p 值调整方法.
- 基于堆叠的参数估计和它们的联合非对称分布的多个边际模型被使用.
- 采用了基于非参数向量的重新采样方法.
- 进行比较时,在各种参数设置下,包括低比例和小样本大小,评估了家庭智能的错误率和功率.
主要成果:
- 基于重新采样的方法在保持家族智能错误率控制的同时显示出优越的功率.
- 多重边际模型方法表现出更保守的行为,但提供了更大的灵活性.
- 这两种方法都与传统的Bonferroni方法进行了比较.
结论:
- 建议使用重抽样方法,因为它在分析多个二进制终点时具有权力平衡和错误控制.
- 多个边际模型提供了一种多功能替代方案,特别适用于复杂的分析和同时的置信区间.
- 这两种新方法均使用国家毒理学计划的毒理学数据集进行了验证.
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