Sarisik Elif, Popovic David, Keeser Daniel, Khuntia Adyasha, Schiltz Kolja, Falkai Peter, Pogarell Oliver, Koutsouleris Nikolaos
Max Planck Fellow Group Precision Psychiatry, Max Planck Institute of Psychiatry, Munich, Germany.
Department of Psychiatry and Psychotherapy, LMU University Hospital, LMU Munich, Munich, Germany.
Schizophr Bull. 2025 May 8;51(3):804-817. doi: 10.1093/schbul/sbae150.
Electroencephalography (EEG) is a noninvasive, cost-effective, and robust tool, which directly measures in vivo neuronal mass activity with high temporal resolution. Combined with state-of-the-art machine learning (ML) techniques, EEG recordings could potentially yield in silico biomarkers of severe mental disorders.
Pathological and physiological aging processes influence the electrophysiological signatures of schizophrenia (SCZ) and major depressive disorder (MDD).
From a single-center cohort (N = 735, 51.6% male) comprising healthy control individuals (HC, N = 245) and inpatients suffering from SCZ (N = 250) or MDD (N = 240), we acquired resting-state 19 channel-EEG recordings. Using repeated nested cross-validation, support vector machine models were trained to (1) classify patients with SCZ or MDD and HC individuals and (2) predict age in HC individuals. The age model was applied to patient groups to calculate Electrophysiological Age Gap Estimation (EphysAGE) as the difference between predicted and chronological age. The links between EphysAGE, diagnosis, and medication were then further explored.
The classification models robustly discriminated SCZ from HC (balanced accuracy, BAC = 72.7%, P < .001), MDD from HC (BAC = 67.0%, P < .001), and SCZ from MDD individuals (BAC = 63.2%, P < .001). Notably, central alpha (8-11 Hz) power decrease was the most consistently predictive feature for SCZ and MDD. Higher EphysAGE was associated with an increased likelihood of being misclassified as SCZ in HC and MDD (ρHC = 0.23, P < .001; ρMDD = 0.17, P = .01).
ML models can extract electrophysiological signatures of MDD and SCZ for potential clinical use. However, the impact of aging processes on diagnostic separability calls for timely application of such models, possibly in early recognition settings.
脑电图(EEG)是一种非侵入性、经济高效且强大的工具,它能够以高时间分辨率直接测量体内神经元群体活动。结合最先进的机器学习(ML)技术,EEG记录有可能产生严重精神障碍的计算机模拟生物标志物。
病理和生理衰老过程会影响精神分裂症(SCZ)和重度抑郁症(MDD)的电生理特征。
从一个单中心队列(N = 735,51.6%为男性)中获取静息状态下的19通道EEG记录,该队列包括健康对照个体(HC,N = 245)以及患有SCZ(N = 250)或MDD(N = 240)的住院患者。使用重复嵌套交叉验证,训练支持向量机模型以(1)区分SCZ或MDD患者与HC个体,以及(2)预测HC个体的年龄。将年龄模型应用于患者组,计算电生理年龄差距估计(EphysAGE),即预测年龄与实际年龄之间的差异。然后进一步探索EphysAGE、诊断和药物治疗之间的联系。
分类模型能够稳健地区分SCZ与HC(平衡准确率,BAC = 72.7%,P <.001)、MDD与HC(BAC = 67.0%,P <.001)以及SCZ与MDD个体(BAC = 63.2%,P <.001)。值得注意的是,中央阿尔法(8 - 11 Hz)功率降低是SCZ和MDD最一致的预测特征。较高的EphysAGE与HC和MDD中被误分类为SCZ的可能性增加相关(ρHC = 0.23,P <.001;ρMDD = 0.17,P =.01)。
ML模型可以提取MDD和SCZ的电生理特征以供潜在的临床使用。然而,衰老过程对诊断可分离性的影响要求及时应用此类模型,可能应用于早期识别环境中。