Putative Mechanisms of Electroconvulsive Therapy in Treatment-Resistant Schizophrenia Examined Using Magnetic Resonance Imaging

IF 4 Q2 NEUROSCIENCES
Neelabja Roy , Dhruva Ithal , Urvakhsh Meherwan Mehta , Rakshathi Basavaraju , Rose Dawn Bharath , Nicolas R. Bolo , Jagadisha Thirthalli , Bangalore N. Gangadhar , Matcheri S. Keshavan
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Abstract

Background

The neural mechanisms of electroconvulsive therapy (ECT) in refractory schizophrenia remain elusive. In the current study, we aimed to identify magnetic resonance imaging (MRI)–derived structural (cortical/subcortical volumes) and functional (resting-state connectivity) brain changes after ECT and their associations with clinical response.

Methods

We used an inductive (whole-brain, hypothesis-free) approach to examine structural and functional brain changes and their association with clinical response (positive symptom reduction) in clozapine-refractory schizophrenia (n = 30) after ECT (median 8 sessions). Furthermore, a deductive approach was used to compare baseline whole-brain MRI data from clozapine-refractory patients (n = 31) to data from clozapine responders (n = 23), thereby identifying regions of interest unique to clozapine-refractory schizophrenia. Changes in these regions of interest post-ECT and their association with clinical response were then examined.

Results

The inductive approach identified volumetric enhancement in the bilateral amygdalae (Cohen’s d = 0.4), which was significantly associated with clinical response (β = −0.01, p = .003). The deductive approach identified posterior cerebellar hyperconnectivity as being unique to clozapine-refractory schizophrenia (d = 1.57), which was associated with baseline positive symptoms (r = 0.36, p = .04). Following ECT, there was a significant reduction in posterior cerebellar hyperconnectivity (d = −0.86), and this reduction was significantly associated with clinical response (β = 0.42, p = .002). Increased hippocampal and frontal volumes, frontoparietal connectivity, and reduced sensorimotor connectivity were also observed but were unrelated to clinical response.

Conclusions

ECT may drive clinical improvement in refractory schizophrenia by increasing amygdala volumes and reducing posterior cerebellar connectivity. Randomized sham-controlled trials can confirm these findings in the future.
核磁共振成像研究电痉挛治疗难治性精神分裂症的可能机制
背景电休克治疗难治性精神分裂症的神经机制尚不清楚。在目前的研究中,我们的目的是确定磁共振成像(MRI)衍生的结构(皮质/皮质下体积)和功能(静息状态连接)脑电痉挛后的变化及其与临床反应的关系。方法采用归纳(全脑,无假设)方法检查氯氮平难治性精神分裂症患者(n = 30)在ECT(中位8次)后脑结构和功能变化及其与临床反应(阳性症状减轻)的关系。此外,采用演绎法比较氯氮平难治性患者(n = 31)和氯氮平应答者(n = 23)的基线全脑MRI数据,从而确定氯氮平难治性精神分裂症独有的感兴趣区域。然后检查ect后这些感兴趣区域的变化及其与临床反应的关系。结果诱导入路发现双侧杏仁核体积增强(Cohen’s d = 0.4),与临床疗效显著相关(β = - 0.01, p = 0.003)。演绎方法确定小脑后部超连通性是氯氮平难治性精神分裂症所特有的(d = 1.57),这与基线阳性症状相关(r = 0.36, p = 0.04)。ECT治疗后,小脑后部超连通性显著降低(d = - 0.86),且这种降低与临床反应显著相关(β = 0.42, p = 0.002)。海马和额叶体积增加,额顶叶连通性和感觉运动连通性减少也被观察到,但与临床反应无关。结论通过增加杏仁核体积和减少小脑后连通性可促进难治性精神分裂症的临床改善。未来的随机模拟对照试验可以证实这些发现。
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来源期刊
Biological psychiatry global open science
Biological psychiatry global open science Psychiatry and Mental Health
CiteScore
4.00
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