TY - JOUR
T1 - Investigating structural subdivisions of the anterior cingulate cortex in schizophrenia, with implications for treatment resistance and glutamatergic levels
AU - Ochi, Ryo
AU - Plitman, Eric
AU - Patel, Raihaan
AU - Tarumi, Ryosuke
AU - Iwata, Yusuke
AU - Tsugawa, Sakiko
AU - Kim, Julia
AU - Honda, Shiori
AU - Noda, Yoshihiro
AU - Uchida, Hiroyuki
AU - Devenyi, Gabriel A.
AU - Mimura, Masaru
AU - Graff-Guerrero, Ariel
AU - Chakravarty, M. Mallar
AU - Nakajima, Shinichiro
N1 - Funding Information:
Funding: This work was supported by the Japan Society for the
Funding Information:
This work was supported by the Japan Society for the Promotion of Science (18H02755), Japan Research Foundation for Clinical Pharmacology, Japan Agency for Medical Research and Development (AMED), Naito Foundation, Takeda Science Foundation and Uehara Memorial Foundation (Noda, Mimura, Nakajima). The funding agency did not contribute to the study design; to the data collection, analyses and interpretation; to the writing of the manuscript; or to the decision to submit the manu script for publication.
Publisher Copyright:
© 2022 CMA Impact Inc. or its licensors.
PY - 2022/1/19
Y1 - 2022/1/19
N2 - Background: Abnormalities in the anterior cingulate cortex (ACC) are thought to play an important role in the pathophysiology of schizophrenia. Given regional variations in ACC structure, the present study aimed to examine ACC structural subdivisions and their relationships to treatment resistance and glutamatergic levels in schizophrenia. Methods: This study included 100 patients with schizophrenia and 52 healthy controls from 2 cohorts. We applied non-negative matrix factorization to identify accurate and stable spatial components of ACC structure. Between groups, we compared ACC structural indices in each spatial component based on treatment resistance or response and tested relationships with ACC glutamate + glutamine levels. Results: We detected reductions in cortical thickness and increases in mean diffusivity in the spatial components on the surface of the cingulate sulcus, especially in patients with treatment-resistant and clozapine-resistant schizophrenia. Notably, mean diffusivity in these components was higher in patients who did not respond to clozapine compared to those who did. Furthermore, these ACC structural alterations were related to elevated ACC glutamate + glutamine levels but not related to symptomatology or antipsychotic dose. Limitations: Sample sizes, cross-sectional findings and mixed antipsychotic status were limitations of this study. Conclusion: This study identified reproducible abnormalities in ACC structures in patients with treatment-resistant and clozapine-resistant schizophrenia. Given that these spatial components play a role in inhibitory control, the present study strengthens the notion that glutamate-related disinhibition is a common biological feature of treatment resistance in schizophrenia.
AB - Background: Abnormalities in the anterior cingulate cortex (ACC) are thought to play an important role in the pathophysiology of schizophrenia. Given regional variations in ACC structure, the present study aimed to examine ACC structural subdivisions and their relationships to treatment resistance and glutamatergic levels in schizophrenia. Methods: This study included 100 patients with schizophrenia and 52 healthy controls from 2 cohorts. We applied non-negative matrix factorization to identify accurate and stable spatial components of ACC structure. Between groups, we compared ACC structural indices in each spatial component based on treatment resistance or response and tested relationships with ACC glutamate + glutamine levels. Results: We detected reductions in cortical thickness and increases in mean diffusivity in the spatial components on the surface of the cingulate sulcus, especially in patients with treatment-resistant and clozapine-resistant schizophrenia. Notably, mean diffusivity in these components was higher in patients who did not respond to clozapine compared to those who did. Furthermore, these ACC structural alterations were related to elevated ACC glutamate + glutamine levels but not related to symptomatology or antipsychotic dose. Limitations: Sample sizes, cross-sectional findings and mixed antipsychotic status were limitations of this study. Conclusion: This study identified reproducible abnormalities in ACC structures in patients with treatment-resistant and clozapine-resistant schizophrenia. Given that these spatial components play a role in inhibitory control, the present study strengthens the notion that glutamate-related disinhibition is a common biological feature of treatment resistance in schizophrenia.
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U2 - 10.1503/jpn.210113
DO - 10.1503/jpn.210113
M3 - Article
C2 - 35027443
AN - SCOPUS:85123192884
SN - 1180-4882
VL - 47
SP - E1-E10
JO - Journal of Psychiatry and Neuroscience
JF - Journal of Psychiatry and Neuroscience
IS - 1
ER -