Stubberud Anker, Gray Robert, Tronvik Erling, Matharu Manjit, Nachev Parashkev
Headache and Facial Pain Group, UCL Queen Square Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK.
High Dimensional Neurology Group, UCL Queen Square Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK.
Brain Commun. 2022 Mar 10;4(3):fcac059. doi: 10.1093/braincomms/fcac059. eCollection 2022.
Responsive to treatment individually, chronic migraine remains strikingly resistant collectively, incurring the second-highest population burden of disability worldwide. A heterogeneity of responsiveness, requiring prolonged-currently heuristic-individual evaluation of available treatments, may reflect a diversity of causal mechanisms, or the failure to identify the most important, single causal factor. Distinguishing between these possibilities, now possible through the application of complex modelling to large-scale data, is critical to determine the optimal approach to identify new interventions in migraine and making the best use of existing ones. Examining a richly phenotyped cohort of 1446 consecutive unselected patients with chronic migraine, here we use causal multitask Gaussian process models to estimate individual treatment effects across 10 classes of preventatives. Such modelling enables us to quantify the accessibility of heterogeneous responsiveness to high-dimensional modelling, to infer the likely scale of the underlying causal diversity. We calculate the treatment effects in the overall population, and the conditional treatment effects among those modelled to respond and compare the true response rates between these two groups. Identifying a difference in response rates between the groups supports a diversity of causal mechanisms. Moreover, we propose a data-driven machine prescription policy, estimating the time-to-response when sequentially trialling preventatives by individualized treatment effects and comparing it to expert guideline sequences. All model performances are quantified out-of-sample. We identify significantly higher true response rates among individuals modelled to respond, compared with the overall population (mean difference of 0.034; 95% confidence interval 0.003-0.065; = 0.033), supporting significant heterogeneity of responsiveness and diverse causal mechanisms. The machine prescription policy yields an estimated 35% reduction in time-to-response (3.750 months; 95% confidence interval 3.507-3.993; < 0.0001) compared with expert guidelines, with no substantive increase in expense per patient. We conclude that the highly distributed mode of causation in chronic migraine necessitates high-dimensional modelling for optimal management. Machine prescription should be considered an essential clinical decision-support tool in the future management of chronic migraine.
尽管慢性偏头痛对治疗的个体反应各异,但总体上仍极具抗性,在全球范围内造成了第二高的残疾人口负担。反应的异质性需要对现有治疗方法进行长期的、目前仍为启发式的个体评估,这可能反映了因果机制的多样性,或者未能识别出最重要的单一因果因素。通过将复杂模型应用于大规模数据,现在可以区分这些可能性,这对于确定识别偏头痛新干预措施的最佳方法以及充分利用现有措施至关重要。在对1446例连续入选的未经选择的慢性偏头痛患者进行丰富表型分析的队列研究中,我们使用因果多任务高斯过程模型来估计10类预防性药物的个体治疗效果。这种建模使我们能够量化异质性反应对高维建模的可及性,从而推断潜在因果多样性的可能规模。我们计算总体人群中的治疗效果,以及建模为有反应者中的条件治疗效果,并比较这两组之间的真实反应率。两组之间反应率的差异支持因果机制的多样性。此外,我们提出了一种数据驱动的机器处方策略,通过个体治疗效果依次试验预防性药物时估计反应时间,并将其与专家指南顺序进行比较。所有模型性能均在样本外进行量化。我们发现,与总体人群相比,建模为有反应者中的真实反应率显著更高(平均差异为0.034;95%置信区间为0.003 - 0.065;P = 0.033),这支持了反应的显著异质性和多样的因果机制。与专家指南相比,机器处方策略估计可将反应时间缩短35%(3.750个月;95%置信区间为3.507 - 3.993;P < 0.0001),且每位患者的费用没有实质性增加。我们得出结论,慢性偏头痛高度分散的病因模式需要高维建模以实现最佳管理。在慢性偏头痛的未来管理中,机器处方应被视为一种重要的临床决策支持工具。