4.5 Article

Association of cortical thickness and cognition with schizophrenia treatment resistance

Journal

PSYCHIATRY AND CLINICAL NEUROSCIENCES
Volume 77, Issue 1, Pages 12-19

Publisher

WILEY
DOI: 10.1111/pcn.13486

Keywords

cognition; cortical thickness; MRI; schizophrenia; treatment-resistant

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Treatment resistance in schizophrenia is associated with reduced cortical thickness in specific brain regions. These regions include the right caudal middle frontal gyrus, superior frontal cortex, fusiform gyrus, pars opercularis of the inferior frontal cortex, and supramarginal cortex. The reductions in cortical thickness in these regions are significantly correlated with cognitive deficits. Moreover, cortical abnormalities in the right caudal middle frontal gyrus, superior frontal cortex, and pars opercularis of the inferior frontal cortex mediate the effects of cognitive deficits on treatment resistance.
Aim: Approximately a third of patients with schizophrenia fail to adequately respond to antipsychotic medications, a condition known as treatment resistance (TR). We aimed to assess cognitive and cortical thickness deficits and their relationship to TR in schizophrenia. Method: We recruited patients with schizophrenia (n = 127), including patients at treatment initiation (n = 45), treatment-responsive patients (n = 40) and TR patients (n = 42), and healthy controls (n = 83). Clinical symptoms, neurocognitive function, and structural images were assessed. We performed group comparisons, and explored association of cortical thickness and cognition with TR. Results: The TR patients showed significantly more severe clinical symptoms and cognitive impairment relative to the treatment-responsive group. Compared to healthy controls, 56 of 68 brain regions showed significantly reduced cortical thickness in patients with schizophrenia. Reductions in five regions were significantly associated with TR (reduction in TR relative to treatment-responsive patients), i.e. in the right caudal middle frontal gyrus, superior frontal cortex, fusiform gyrus, pars opercularis of the inferior frontal cortex, and supramarginal cortex. Cognition deficits were also significantly correlated with cortical thickness in these five regions in patients with schizophrenia. Cortical thickness of the right caudal middle frontal gyrus, superior frontal cortex and pars opercularis of the inferior frontal cortex also significantly mediated effects of cognitive deficits on TR. Conclusion: Treatment resistance in schizophrenia was associated with reduced thickness in the right caudal middle frontal gyrus, superior frontal cortex, fusiform gyrus, pars opercularis of the inferior frontal cortex, and supramarginal cortex. Cortical abnormalities further mediate cognitive deficits known to be associated with TR.

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