The immediate alteration of cerebellar Glx/GABA and cerebello-thalamo-cortical connectivity in patients with schizophrenia after cerebellar TMS

Abstract Cerebellar dysfunction is a key aspect of schizophrenia, with the cerebello-thalamo-cortical (CTC) hyperconnectivity serving as a neural signature. Abnormalities in gamma-aminobutyric acid (GABA) and glutamate + glutamine (Glx) levels also contribute to this pathology. Transcranial magnetic...

Full description

Saved in:
Bibliographic Details
Main Authors: Chenyang Yao, Youjin Zhao, Qian Zhang, Ziyuan Zhao, Kai Ai, Bo Zhang, Su Lui
Format: Article
Language:English
Published: Nature Portfolio 2025-02-01
Series:Schizophrenia
Online Access:https://doi.org/10.1038/s41537-025-00563-8
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1823861992704704512
author Chenyang Yao
Youjin Zhao
Qian Zhang
Ziyuan Zhao
Kai Ai
Bo Zhang
Su Lui
author_facet Chenyang Yao
Youjin Zhao
Qian Zhang
Ziyuan Zhao
Kai Ai
Bo Zhang
Su Lui
author_sort Chenyang Yao
collection DOAJ
description Abstract Cerebellar dysfunction is a key aspect of schizophrenia, with the cerebello-thalamo-cortical (CTC) hyperconnectivity serving as a neural signature. Abnormalities in gamma-aminobutyric acid (GABA) and glutamate + glutamine (Glx) levels also contribute to this pathology. Transcranial magnetic stimulation (TMS) applied to the cerebellum shows potential in alleviating schizophrenia symptoms, possibly by modulating functional connectivity or neurotransmitter levels. This study aims to explore the immediate effects of cerebellar TMS on CTC circuitry and neurotransmitter levels to elucidate its therapeutic mechanisms in schizophrenia.The study involved 19 stable schizophrenia patients and 26 healthy controls, diagnosed according to DSM-V criteria and assessed for symptom severity using the Positive and Negative Syndrome Scale (PANSS). MRI scans were conducted pre- and post-TMS to detect changes in CTC functional connectivity, GABA, Glx, and Glx/GABA. Linear Mixed-Effects Model (LMEM) and two-sample tests were employed to analyze changes in these variables from baseline to post-TMS. Pearson’s correlation analysis was conducted to examine the relationships among these variables and their association with PANSS scores. Mediation analyses were employed to investigate whether GABA and/or Glx serve as potential mediators of CTC hyperconnectivity in patients with schizophrenia. Schizophrenia patients exhibit CTC hyperconnectivity, which remains at a relatively stable level after cerebellar TMS. Compared to healthy controls, schizophrenia patients have significantly higher cerebellar GABA levels, and cerebellar GABA has a significant mediation effect on CTC hyperconnectivity in patients. The Glx/GABA ratio was associated with the severity of clinical symptoms in patients, and cerebellar TMS partially normalized this ratio. Our findings demonstrate that aberrant cerebellar GABA levels contribute to CTC hyperconnectivity in schizophrenia. Additionally, our study shows that cerebellar TMS can increase Glx levels in schizophrenia patients, leading to the normalization of the Glx/GABA ratio, which may contribute to the therapeutic effects of TMS in schizophrenia.
format Article
id doaj-art-a7246b83f7cd46ac94442f528603c38f
institution Kabale University
issn 2754-6993
language English
publishDate 2025-02-01
publisher Nature Portfolio
record_format Article
series Schizophrenia
spelling doaj-art-a7246b83f7cd46ac94442f528603c38f2025-02-09T12:42:06ZengNature PortfolioSchizophrenia2754-69932025-02-0111111010.1038/s41537-025-00563-8The immediate alteration of cerebellar Glx/GABA and cerebello-thalamo-cortical connectivity in patients with schizophrenia after cerebellar TMSChenyang Yao0Youjin Zhao1Qian Zhang2Ziyuan Zhao3Kai Ai4Bo Zhang5Su Lui6Department of Radiology, and Functional and Molecular Imaging Key Laboratory of Sichuan Province, West China Hospital of Sichuan UniversityDepartment of Radiology, and Functional and Molecular Imaging Key Laboratory of Sichuan Province, West China Hospital of Sichuan UniversityDepartment of Radiology, and Functional and Molecular Imaging Key Laboratory of Sichuan Province, West China Hospital of Sichuan UniversityDepartment of Radiology, and Functional and Molecular Imaging Key Laboratory of Sichuan Province, West China Hospital of Sichuan UniversityDepartment of Clinical and Technical Supports, Philips HealthcareMental Health Center, West China Hospital of Sichuan UniversityDepartment of Radiology, and Functional and Molecular Imaging Key Laboratory of Sichuan Province, West China Hospital of Sichuan UniversityAbstract Cerebellar dysfunction is a key aspect of schizophrenia, with the cerebello-thalamo-cortical (CTC) hyperconnectivity serving as a neural signature. Abnormalities in gamma-aminobutyric acid (GABA) and glutamate + glutamine (Glx) levels also contribute to this pathology. Transcranial magnetic stimulation (TMS) applied to the cerebellum shows potential in alleviating schizophrenia symptoms, possibly by modulating functional connectivity or neurotransmitter levels. This study aims to explore the immediate effects of cerebellar TMS on CTC circuitry and neurotransmitter levels to elucidate its therapeutic mechanisms in schizophrenia.The study involved 19 stable schizophrenia patients and 26 healthy controls, diagnosed according to DSM-V criteria and assessed for symptom severity using the Positive and Negative Syndrome Scale (PANSS). MRI scans were conducted pre- and post-TMS to detect changes in CTC functional connectivity, GABA, Glx, and Glx/GABA. Linear Mixed-Effects Model (LMEM) and two-sample tests were employed to analyze changes in these variables from baseline to post-TMS. Pearson’s correlation analysis was conducted to examine the relationships among these variables and their association with PANSS scores. Mediation analyses were employed to investigate whether GABA and/or Glx serve as potential mediators of CTC hyperconnectivity in patients with schizophrenia. Schizophrenia patients exhibit CTC hyperconnectivity, which remains at a relatively stable level after cerebellar TMS. Compared to healthy controls, schizophrenia patients have significantly higher cerebellar GABA levels, and cerebellar GABA has a significant mediation effect on CTC hyperconnectivity in patients. The Glx/GABA ratio was associated with the severity of clinical symptoms in patients, and cerebellar TMS partially normalized this ratio. Our findings demonstrate that aberrant cerebellar GABA levels contribute to CTC hyperconnectivity in schizophrenia. Additionally, our study shows that cerebellar TMS can increase Glx levels in schizophrenia patients, leading to the normalization of the Glx/GABA ratio, which may contribute to the therapeutic effects of TMS in schizophrenia.https://doi.org/10.1038/s41537-025-00563-8
spellingShingle Chenyang Yao
Youjin Zhao
Qian Zhang
Ziyuan Zhao
Kai Ai
Bo Zhang
Su Lui
The immediate alteration of cerebellar Glx/GABA and cerebello-thalamo-cortical connectivity in patients with schizophrenia after cerebellar TMS
Schizophrenia
title The immediate alteration of cerebellar Glx/GABA and cerebello-thalamo-cortical connectivity in patients with schizophrenia after cerebellar TMS
title_full The immediate alteration of cerebellar Glx/GABA and cerebello-thalamo-cortical connectivity in patients with schizophrenia after cerebellar TMS
title_fullStr The immediate alteration of cerebellar Glx/GABA and cerebello-thalamo-cortical connectivity in patients with schizophrenia after cerebellar TMS
title_full_unstemmed The immediate alteration of cerebellar Glx/GABA and cerebello-thalamo-cortical connectivity in patients with schizophrenia after cerebellar TMS
title_short The immediate alteration of cerebellar Glx/GABA and cerebello-thalamo-cortical connectivity in patients with schizophrenia after cerebellar TMS
title_sort immediate alteration of cerebellar glx gaba and cerebello thalamo cortical connectivity in patients with schizophrenia after cerebellar tms
url https://doi.org/10.1038/s41537-025-00563-8
work_keys_str_mv AT chenyangyao theimmediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT youjinzhao theimmediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT qianzhang theimmediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT ziyuanzhao theimmediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT kaiai theimmediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT bozhang theimmediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT sului theimmediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT chenyangyao immediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT youjinzhao immediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT qianzhang immediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT ziyuanzhao immediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT kaiai immediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT bozhang immediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms
AT sului immediatealterationofcerebellarglxgabaandcerebellothalamocorticalconnectivityinpatientswithschizophreniaaftercerebellartms