Aryeh Dworkin , Diego Jiménez-Jiménez , Charlotte Ravenscroft , Francesco Turco , Chloe Johnson , Fahmida A. Chowdhury , Joao Pizarro , Sasha D'Ambrosio , Sanjay M. Sisodiya , Umesh Vivekananda , Simona Balestrini
{"title":"癫后性精神病的TMS-EEG分析","authors":"Aryeh Dworkin , Diego Jiménez-Jiménez , Charlotte Ravenscroft , Francesco Turco , Chloe Johnson , Fahmida A. Chowdhury , Joao Pizarro , Sasha D'Ambrosio , Sanjay M. Sisodiya , Umesh Vivekananda , Simona Balestrini","doi":"10.1016/j.schres.2025.06.015","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Postictal psychosis (PIP) is a poorly understood complication affecting 2 % of individuals with epilepsy. Genomic and neuroimaging studies suggest parallels with schizophrenia.</div></div><div><h3>Objectives</h3><div>To determine whether Transcranial Magnetic Stimulation coupled with Electroencephalography (TMS-EEG), can reveal schizophrenia-like changes in PIP, especially in Natural Frequency (NF), gamma band Event-Related Spectral Perturbation (ERSP), the N100 peak, and global mean field power (GMFP).</div></div><div><h3>Methods</h3><div>We applied TMS-EEG targeting the non-dominant hemisphere premotor area in people with focal epilepsy (PWE) with a history of PIP (<em>n</em> = 7) and PWE without any history of psychosis (<em>n</em> = 14). Two-tailed <em>t</em>-tests were applied to TMS-EEG metrics previously studied in schizophrenia to look for differences between the groups, with subgroup analyses excluding participants using benzodiazepines.</div></div><div><h3>Results</h3><div>Demographic and clinical characteristics were similar across the two groups. No significant differences were seen in NF (<em>p</em> = 0.98). We observed a delayed N100 peak latency in the PIP group when excluding those with regular benzodiazepine use (<em>p</em> = 0.05) and increased global mean field power during the 400-600 ms phase of the TEP (<em>p</em> = 0.02). Mean ERSP within the gamma band was lower in the PIP group, though this did not reach statistical significance (<em>p</em> = 0.08).</div></div><div><h3>Conclusion</h3><div>This is the first study to apply TMS-EEG in individuals with PIP, demonstrating feasibility and providing methodological insights for future studies. Preliminary findings, including increased GMFP and delayed N100 latency in PIP, suggest possible disruptions in cortical excitability similar to schizophrenia, warranting further investigation.</div></div>","PeriodicalId":21417,"journal":{"name":"Schizophrenia Research","volume":"282 ","pages":"Pages 176-183"},"PeriodicalIF":3.5000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"TMS-EEG in postictal psychosis of epilepsy\",\"authors\":\"Aryeh Dworkin , Diego Jiménez-Jiménez , Charlotte Ravenscroft , Francesco Turco , Chloe Johnson , Fahmida A. Chowdhury , Joao Pizarro , Sasha D'Ambrosio , Sanjay M. Sisodiya , Umesh Vivekananda , Simona Balestrini\",\"doi\":\"10.1016/j.schres.2025.06.015\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Postictal psychosis (PIP) is a poorly understood complication affecting 2 % of individuals with epilepsy. Genomic and neuroimaging studies suggest parallels with schizophrenia.</div></div><div><h3>Objectives</h3><div>To determine whether Transcranial Magnetic Stimulation coupled with Electroencephalography (TMS-EEG), can reveal schizophrenia-like changes in PIP, especially in Natural Frequency (NF), gamma band Event-Related Spectral Perturbation (ERSP), the N100 peak, and global mean field power (GMFP).</div></div><div><h3>Methods</h3><div>We applied TMS-EEG targeting the non-dominant hemisphere premotor area in people with focal epilepsy (PWE) with a history of PIP (<em>n</em> = 7) and PWE without any history of psychosis (<em>n</em> = 14). Two-tailed <em>t</em>-tests were applied to TMS-EEG metrics previously studied in schizophrenia to look for differences between the groups, with subgroup analyses excluding participants using benzodiazepines.</div></div><div><h3>Results</h3><div>Demographic and clinical characteristics were similar across the two groups. No significant differences were seen in NF (<em>p</em> = 0.98). We observed a delayed N100 peak latency in the PIP group when excluding those with regular benzodiazepine use (<em>p</em> = 0.05) and increased global mean field power during the 400-600 ms phase of the TEP (<em>p</em> = 0.02). Mean ERSP within the gamma band was lower in the PIP group, though this did not reach statistical significance (<em>p</em> = 0.08).</div></div><div><h3>Conclusion</h3><div>This is the first study to apply TMS-EEG in individuals with PIP, demonstrating feasibility and providing methodological insights for future studies. Preliminary findings, including increased GMFP and delayed N100 latency in PIP, suggest possible disruptions in cortical excitability similar to schizophrenia, warranting further investigation.</div></div>\",\"PeriodicalId\":21417,\"journal\":{\"name\":\"Schizophrenia Research\",\"volume\":\"282 \",\"pages\":\"Pages 176-183\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-07-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Schizophrenia Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0920996425002312\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PSYCHIATRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Schizophrenia Research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920996425002312","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
Postictal psychosis (PIP) is a poorly understood complication affecting 2 % of individuals with epilepsy. Genomic and neuroimaging studies suggest parallels with schizophrenia.
Objectives
To determine whether Transcranial Magnetic Stimulation coupled with Electroencephalography (TMS-EEG), can reveal schizophrenia-like changes in PIP, especially in Natural Frequency (NF), gamma band Event-Related Spectral Perturbation (ERSP), the N100 peak, and global mean field power (GMFP).
Methods
We applied TMS-EEG targeting the non-dominant hemisphere premotor area in people with focal epilepsy (PWE) with a history of PIP (n = 7) and PWE without any history of psychosis (n = 14). Two-tailed t-tests were applied to TMS-EEG metrics previously studied in schizophrenia to look for differences between the groups, with subgroup analyses excluding participants using benzodiazepines.
Results
Demographic and clinical characteristics were similar across the two groups. No significant differences were seen in NF (p = 0.98). We observed a delayed N100 peak latency in the PIP group when excluding those with regular benzodiazepine use (p = 0.05) and increased global mean field power during the 400-600 ms phase of the TEP (p = 0.02). Mean ERSP within the gamma band was lower in the PIP group, though this did not reach statistical significance (p = 0.08).
Conclusion
This is the first study to apply TMS-EEG in individuals with PIP, demonstrating feasibility and providing methodological insights for future studies. Preliminary findings, including increased GMFP and delayed N100 latency in PIP, suggest possible disruptions in cortical excitability similar to schizophrenia, warranting further investigation.
期刊介绍:
As official journal of the Schizophrenia International Research Society (SIRS) Schizophrenia Research is THE journal of choice for international researchers and clinicians to share their work with the global schizophrenia research community. More than 6000 institutes have online or print (or both) access to this journal - the largest specialist journal in the field, with the largest readership!
Schizophrenia Research''s time to first decision is as fast as 6 weeks and its publishing speed is as fast as 4 weeks until online publication (corrected proof/Article in Press) after acceptance and 14 weeks from acceptance until publication in a printed issue.
The journal publishes novel papers that really contribute to understanding the biology and treatment of schizophrenic disorders; Schizophrenia Research brings together biological, clinical and psychological research in order to stimulate the synthesis of findings from all disciplines involved in improving patient outcomes in schizophrenia.