University of Ottawa Institute of Mental Health Research, 1145 Carling Avenue, Ottawa, ON, K1Z 7K4, Canada.
Mol Psychiatry. 2024 Feb;29(2):425-438. doi: 10.1038/s41380-023-02337-z. Epub 2024 Jan 16.
Schizophrenia (SCZ) is a complex disorder in which various pathophysiological models have been postulated. Brain imaging studies using EEG/MEG and fMRI show altered amplitude and, more recently, decrease in phase coherence in response to external stimuli. What are the dynamic mechanisms of such phase incoherence, and can it serve as a differential-diagnostic marker? Addressing this gap in our knowledge, we uniquely combine a review of previous findings, novel empirical data, and computational-dynamic simulation. The main findings are: (i) the review shows decreased phase coherence in SCZ across a variety of different tasks and frequencies, e.g., task- and frequency-unspecific, which is further supported by our own novel data; (ii) our own data demonstrate diagnostic specificity of decreased phase coherence for SCZ as distinguished from major depressive disorder; (iii) simulation data exhibit increased phase offset in SCZ leading to a precision index, in the millisecond range, of the phase coherence relative to the timing of the external stimulus. Together, we demonstrate the key role of temporal imprecision in phase coherence of SCZ, including its mechanisms (phase offsets, precision index) on the basis of which we propose a phase-based temporal imprecision model of psychosis (PTP). The PTP targets a deeper dynamic layer of a basic disturbance. This converges well with other models of psychosis like the basic self-disturbance and time-space experience changes, as discussed in phenomenological and spatiotemporal psychopathology, as well as with the models of aberrant predictive coding and disconnection as in computational psychiatry. Finally, our results show that temporal imprecision as manifest in decreased phase coherence is a promising candidate biomarker for clinical differential diagnosis of SCZ, and more broadly, psychosis.
精神分裂症(SCZ)是一种复杂的疾病,已经提出了多种病理生理学模型。使用 EEG/MEG 和 fMRI 的脑成像研究表明,对外界刺激的反应幅度发生了改变,最近相位相干性也降低了。这种相位失谐的动态机制是什么,它能否作为一种鉴别诊断标志物?为了弥补我们知识中的这一空白,我们独特地结合了对以前研究结果的综述、新的经验数据和计算动力学模拟。主要发现有:(i)综述表明,在各种不同的任务和频率下,SCZ 的相位相干性降低,例如任务和频率非特异性,这进一步得到了我们自己的新数据的支持;(ii)我们自己的数据表明,与重度抑郁症相比,相位相干性降低对 SCZ 具有诊断特异性;(iii)模拟数据显示,SCZ 中的相位偏移增加,导致相位相干性相对于外部刺激时间的精度指数在毫秒范围内。综上所述,我们证明了 SCZ 相位相干性中时间精度的关键作用,包括其机制(相位偏移、精度指数),在此基础上,我们提出了一种基于相位的精神错乱时间不精确模型(PTP)。PTP 针对的是基本干扰的更深层次的动态层。这与其他精神病模型很好地吻合,如基本的自我干扰和时空体验变化,正如在现象学和时空精神病学中讨论的那样,以及在计算精神病学中讨论的异常预测编码和连接中断模型也是如此。最后,我们的结果表明,以相位相干性降低为表现的时间不精确性是 SCZ 临床鉴别诊断的一个很有前途的候选生物标志物,更广泛地说,也是精神病的候选生物标志物。