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. 2023 Jun;53(8):3500-3510.
doi: 10.1017/S0033291722000058. Epub 2022 Feb 15.

Ameliorative patterns of grey matter in patients with first-episode and treatment-naïve schizophrenia

Affiliations

Ameliorative patterns of grey matter in patients with first-episode and treatment-naïve schizophrenia

Mingli Li et al. Psychol Med. 2023 Jun.

Abstract

Background: Grey matter (GM) reduction is a consistent observation in established late stages of schizophrenia, but patients in the untreated early stages of illness display an increase as well as a decrease in GM distribution relative to healthy controls (HC). The relative excess of GM may indicate putative compensatory responses, though to date its relevance is unclear.

Methods: 343 first-episode treatment-naïve patients with schizophrenia (FES) and 342 HC were recruited. Multivariate source-based morphometry was performed to identify covarying 'networks' of grey matter concentration (GMC). Neurocognitive scores using the Cambridge Neuropsychological Test Automated Battery (CANTAB) and symptom burden using the Positive and Negative Symptoms Scale (PANSS) were obtained. Bivariate linear relationships between GMC and cognition/symptoms were studied.

Results: Compared to healthy subjects, FES had prominently lower GMC in two components; the first consists of the anterior insula, inferior frontal gyrus, anterior cingulate and the second component with the superior temporal gyrus, precuneus, inferior/superior parietal lobule, cuneus, and lingual gyrus. Higher GMC was seen in adjacent areas of the middle and superior temporal gyrus, middle frontal gyrus, inferior parietal cortex and putamen. Greater GMC of this component was associated with lower duration of untreated psychosis, less severe positive symptoms and better performance on cognitive tests.

Conclusions: In untreated stages of schizophrenia, both a distributed lower and higher GMC is observable. While the higher GMC is relatively modest, it occurs across frontoparietal, temporal and subcortical regions in association with reduced illness burden suggesting a compensatory role for higher GMC in the early stages of schizophrenia.

Keywords: compensatory; early intervention; morphometry; neurocognition; psychosis.

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Conflict of interest statement

LP reports personal fees from Janssen Canada, Otsuka Canada, SPMM Course Limited, UK, Canadian Psychiatric Association; book royalties from Oxford University Press; investigator-initiated educational grants from Janssen Canada, Sunovion and Otsuka Canada outside the submitted work. All other authors report no relevant conflicts.

Figures

Fig. 1.
Fig. 1.
Spatial maps of the four components showing (NN-FES v. HC) group effect. All are thresholded at |z| > 3 and superimposed onto a standard brain template provided by MRICron. The colour bar indicates the colour mapping for the normalised component weights. HC > NN-FES: component 4, 24; NN-FES > HC: component 13, 26. SBM, source-based morphometry; HC, healthy control; NN-FES, first-episode neuroleptic-naïve patients with schizophreniform psychosis and schizophrenia.
Fig. 2.
Fig. 2.
Patterns of grey matter alterations in first-episode neuroleptic-naïve patients with schizophreniform psychosis and schizophrenia. Abbreviations: GMC, grey matter concentration; NN-FES, first-episode neuroleptic-naïve patients with schizophreniform psychosis and schizophrenia; SPL, Superior Parietal Lobule; IPL, Inferior Parietal Lobule; STG, Superior Temporal Gyrus; ACC, Anterior Cingulate Cortex; IFG, Inferior Frontal Gyrus; MTG, Middle Temporal Gyrus. Component 4 including insular, ACC, STG and IFG regions is shown in red; Component 24 including precuneus and cuneus, lingual gyrus, SPL, IPL and STG is shown in yellow; Component 26 including MFG, MTG, IPL, STG and putamen is shown in blue; Component 13 including cerebellar Tonsil and inferior Semi-Lunar Lobule is shown in purple.

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