Associations Between Structural Covariance Network and Antipsychotic Treatment Response in Schizophrenia

Author:

Tsugawa Sakiko1,Honda Shiori1,Noda Yoshihiro1,Wannan Cassandra2,Zalesky Andrew3,Tarumi Ryosuke14,Iwata Yusuke5,Ogyu Kamiyu16,Plitman Eric7ORCID,Ueno Fumihiko18,Mimura Masaru1,Uchida Hiroyuki1ORCID,Chakravarty Mallar79,Graff-Guerrero Ariel8,Nakajima Shinichiro1

Affiliation:

1. Department of Neuropsychiatry, Keio University , Tokyo , Japan

2. Department of Psychiatry, University of Melbourne , Melbourne , Australia

3. Department of Biomedical Engineering, Melbourne School of Engineering, the University of Melbourne , Melbourne , Australia

4. Department of Psychiatry, Komagino Hospital , Tokyo , Japan

5. Department of Neuropsychiatry, University of Yamanashi , Yamanashi , Japan

6. Department of Psychiatry, National Hospital Organization Shimofusa Psychiatric Medical Center , Chiba , Japan

7. Department of Psychiatry, McGill University , Montreal, QC , Canada

8. Department of Psychiatry, University of Toronto , Toronto, ON , Canada

9. Computational Brain Anatomy Laboratory, Cerebral Imaging Centre, Douglas Mental Health University Institute , Montreal, QC , Canada

Abstract

Abstract Background and Hypothesis Schizophrenia is associated with widespread cortical thinning and abnormality in the structural covariance network, which may reflect connectome alterations due to treatment effect or disease progression. Notably, patients with treatment-resistant schizophrenia (TRS) have stronger and more widespread cortical thinning, but it remains unclear whether structural covariance is associated with treatment response in schizophrenia. Study Design We organized a multicenter magnetic resonance imaging study to assess structural covariance in a large population of TRS and non-TRS, who had been resistant and responsive to non-clozapine antipsychotics, respectively. Whole-brain structural covariance for cortical thickness was assessed in 102 patients with TRS, 77 patients with non-TRS, and 79 healthy controls (HC). Network-based statistics were used to examine the difference in structural covariance networks among the 3 groups. Moreover, the relationship between altered individual differentiated structural covariance and clinico-demographics was also explored. Study Results Patients with non-TRS exhibited greater structural covariance compared with HC, mainly in the fronto-temporal and fronto-occipital regions, while there were no significant differences in structural covariance between TRS and non-TRS or HC. Higher individual differentiated structural covariance was associated with lower general scores of the Positive and Negative Syndrome Scale in the non-TRS group, but not in the TRS group. Conclusions These findings suggest that reconfiguration of brain networks via coordinated cortical thinning is related to treatment response in schizophrenia. Further longitudinal studies are warranted to confirm if greater structural covariance could serve as a marker for treatment response in this disease.

Funder

Japan Society for the Promotion of Science

Takeda Science Foundation

Watanabe Foundation

Uehara Memorial Foundation

Inokashira Hospital Research Foundation

Ontario Mental Health Foundation

Canadian Institutes of Health Research

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

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