Center for Lifespan Changes in Brain and Cognition, University of Oslo, Pb. 1094 Blindern, Oslo 0317, Norway.
Center for Lifespan Psychology, Max Planck Institute for Human Development, Berlin, Germany; Max Planck UCL Centre for Computational Psychiatry and Ageing Research, Berlin, Germany.
Neuroimage. 2021 Jan 1;224:117416. doi: 10.1016/j.neuroimage.2020.117416. Epub 2020 Oct 2.
Analyzing data from multiple neuroimaging studies has great potential in terms of increasing statistical power, enabling detection of effects of smaller magnitude than would be possible when analyzing each study separately and also allowing to systematically investigate between-study differences. Restrictions due to privacy or proprietary data as well as more practical concerns can make it hard to share neuroimaging datasets, such that analyzing all data in a common location might be impractical or impossible. Meta-analytic methods provide a way to overcome this issue, by combining aggregated quantities like model parameters or risk ratios. Most meta-analytic tools focus on parametric statistical models, and methods for meta-analyzing semi-parametric models like generalized additive models have not been well developed. Parametric models are often not appropriate in neuroimaging, where for instance age-brain relationships may take forms that are difficult to accurately describe using such models. In this paper we introduce meta-GAM, a method for meta-analysis of generalized additive models which does not require individual participant data, and hence is suitable for increasing statistical power while upholding privacy and other regulatory concerns. We extend previous works by enabling the analysis of multiple model terms as well as multivariate smooth functions. In addition, we show how meta-analytic p-values can be computed for smooth terms. The proposed methods are shown to perform well in simulation experiments, and are demonstrated in a real data analysis on hippocampal volume and self-reported sleep quality data from the Lifebrain consortium. We argue that application of meta-GAM is especially beneficial in lifespan neuroscience and imaging genetics. The methods are implemented in an accompanying R package metagam, which is also demonstrated.
分析来自多个神经影像学研究的数据在增加统计效力方面具有很大的潜力,能够检测到比分别分析每个研究时更小的效应,并且还能够系统地研究研究之间的差异。由于隐私或专有数据的限制以及更实际的考虑因素,可能难以共享神经影像学数据集,因此在一个共同的位置分析所有数据可能是不切实际的或不可能的。元分析方法提供了一种克服这个问题的方法,通过合并聚合数量,如模型参数或风险比。大多数元分析工具都集中在参数统计模型上,而用于元分析半参数模型(如广义加性模型)的方法尚未得到很好的发展。参数模型在神经影像学中通常不合适,例如年龄与大脑之间的关系可能采用难以使用此类模型准确描述的形式。在本文中,我们介绍了 meta-GAM,这是一种用于元分析广义加性模型的方法,不需要个体参与者数据,因此适合在维护隐私和其他监管问题的同时增加统计效力。我们通过允许分析多个模型项以及多元平滑函数扩展了以前的工作。此外,我们展示了如何为平滑项计算元分析 p 值。拟议的方法在模拟实验中表现良好,并在 Lifebrain consortium 的海马体积和自我报告的睡眠质量数据的真实数据分析中进行了演示。我们认为,meta-GAM 的应用在寿命神经科学和成像遗传学中尤其有益。该方法在一个配套的 R 包 metagam 中实现,也进行了演示。