神经影像学
电休克疗法
重性抑郁障碍
模式
磁共振成像
心理学
医学
临床心理学
精神科
放射科
心情
精神分裂症(面向对象编程)
社会科学
社会学
作者
Willem B. Bruin,Leif Oltedal,Hauke Bartsch,Chris Abbott,Miklós Árgyelán,Tracy Barbour,Joan A. Camprodon,Samadrita Roy Chowdhury,Randall Espinoza,Peter Mulders,Katherine L. Narr,Mardien L. Oudega,Didi Rhebergen,Freek ten Doesschate,Indira Tendolkar,Philip van Eijndhoven,Eric van Exel,Mike van Verseveld,Benjamin Wade,Jeroen van Waarde,Paul Zhutovsky,Annemiek Dols,Guido van Wingen
标识
DOI:10.1017/s0033291723002040
摘要
Abstract Background Electroconvulsive therapy (ECT) is the most effective intervention for patients with treatment resistant depression. A clinical decision support tool could guide patient selection to improve the overall response rate and avoid ineffective treatments with adverse effects. Initial small-scale, monocenter studies indicate that both structural magnetic resonance imaging (sMRI) and functional MRI (fMRI) biomarkers may predict ECT outcome, but it is not known whether those results can generalize to data from other centers. The objective of this study was to develop and validate neuroimaging biomarkers for ECT outcome in a multicenter setting. Methods Multimodal data (i.e. clinical, sMRI and resting-state fMRI) were collected from seven centers of the Global ECT-MRI Research Collaboration (GEMRIC). We used data from 189 depressed patients to evaluate which data modalities or combinations thereof could provide the best predictions for treatment remission (HAM-D score ⩽7) using a support vector machine classifier. Results Remission classification using a combination of gray matter volume and functional connectivity led to good performing models with average 0.82–0.83 area under the curve (AUC) when trained and tested on samples coming from the three largest centers ( N = 109), and remained acceptable when validated using leave-one-site-out cross-validation (0.70–0.73 AUC). Conclusions These results show that multimodal neuroimaging data can be used to predict remission with ECT for individual patients across different treatment centers, despite significant variability in clinical characteristics across centers. Future development of a clinical decision support tool applying these biomarkers may be feasible.
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