Parsons Sam, McCormick Ethan M
Cognitive Neuroscience Department, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.
Cognitive Neuroscience Department, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands; Methodology & Statistics Department, Institute of Psychology, Leiden University, Leiden, The Netherlands.
Dev Cogn Neurosci. 2024 Apr;66:101353. doi: 10.1016/j.dcn.2024.101353. Epub 2024 Feb 5.
Emerging neuroimaging studies investigating changes in the brain aim to collect sufficient data points to examine trajectories of change across key developmental periods. Yet, current studies are often constrained by the number of time points available now. We demonstrate that these constraints should be taken seriously and that studies with two time points should focus on particular questions (e.g., group-level or intervention effects), while complex questions of individual differences and investigations into causes and consequences of those differences should be deferred until additional time points can be incorporated into models of change. We generated underlying longitudinal data and fit models with 2, 3, 4, and 5 time points across 1000 samples. While fixed effects could be recovered on average even with few time points, recovery of individual differences was particularly poor for the two time point model, correlating at r = 0.41 with the true individual parameters - meaning these scores share only 16.8% of variance As expected, models with more time points recovered the growth parameter more accurately; yet parameter recovery for the three time point model was still low, correlating around r = 0.57. We argue that preliminary analyses on early subsets of time points in longitudinal analyses should focus on these average or group-level effects and that individual difference questions should be addressed in samples that maximize the number of time points available. We conclude with recommendations for researchers using early time point models, including ideas for preregistration, careful interpretation of 2 time point results, and treating longitudinal analyses as dynamic, where early findings are updated as additional information becomes available.
新兴的神经影像学研究旨在通过收集足够的数据点来研究大脑在关键发育阶段的变化轨迹。然而,目前的研究常常受到现有时间点数量的限制。我们证明,这些限制应得到重视,双时间点研究应聚焦于特定问题(如组间水平或干预效果),而关于个体差异的复杂问题以及对这些差异的因果关系的研究应推迟到更多时间点纳入变化模型之后。我们生成了基础纵向数据,并在1000个样本中拟合了包含2、3、4和5个时间点的模型。虽然即使时间点较少,固定效应平均仍可恢复,但双时间点模型对个体差异的恢复尤其差,与真实个体参数的相关性为r = 0.41——这意味着这些分数仅共享16.8%的方差。正如预期的那样,时间点更多的模型能更准确地恢复生长参数;然而,三时间点模型的参数恢复仍然较低,相关性约为r = 0.57。我们认为,纵向分析中对早期时间点子集的初步分析应聚焦于这些平均或组间水平的效应,个体差异问题应在能最大化可用时间点数量的样本中进行研究。我们最后为使用早期时间点模型的研究人员提供了建议,包括预注册的思路、对双时间点结果的谨慎解读,以及将纵向分析视为动态过程,随着更多信息的获取不断更新早期发现。