Howes Oliver D, Chapman George E
Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Faculty of Medicine, MRC Laboratory of Medical Sciences, Imperial College London, London, UK.
Psychol Med. 2024 Oct 4;54(12):1-4. doi: 10.1017/S0033291724001971.
Meta-analyses traditionally compare the difference in means between groups for one or more outcomes of interest. However, they do not compare the spread of data (variability), which could mean that important effects and/or subgroups are missed. To address this, methods to compare variability meta-analytically have recently been developed, making it timely to review them and consider their strengths, weaknesses, and implementation. Using published data from trials in major depression, we demonstrate how the spread of data can impact both overall effect size and the frequency of extreme observations within studies, with potentially important implications for conclusions of meta-analyses, such as the clinical significance of findings. We then describe two methods for assessing group differences in variability meta-analytically: the variance ratio (VR) and coefficient of variation ratio (CVR). We consider the reporting and interpretation of these measures and how they differ from the assessment of heterogeneity between studies. We propose general benchmarks as a guideline for interpreting VR and CVR effects as small, medium, or large. Finally, we discuss some important limitations and practical considerations of VR and CVR and consider the value of integrating variability measures into meta-analyses.
传统的荟萃分析比较一组或多组感兴趣的结果之间的均值差异。然而,它们并不比较数据的离散程度(变异性),这可能意味着重要的效应和/或亚组会被遗漏。为了解决这个问题,最近已经开发出了以荟萃分析方式比较变异性的方法,因此及时对这些方法进行综述并考虑它们的优缺点及应用是很有必要的。利用来自重度抑郁症试验的已发表数据,我们展示了数据的离散程度如何影响研究中的总体效应大小和极端观察值的频率,这对荟萃分析的结论可能具有潜在的重要意义,比如研究结果的临床意义。然后,我们描述了两种以荟萃分析方式评估组间变异性差异的方法:方差比(VR)和变异系数比(CVR)。我们考虑这些指标的报告和解释,以及它们与研究间异质性评估的差异。我们提出通用的基准作为将VR和CVR效应解释为小、中或大效应的指导原则。最后,我们讨论了VR和CVR的一些重要局限性及实际考量,并考虑将变异性指标纳入荟萃分析的价值。