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Background: Both brain structural abnormalities and neurocognitive impairments are core features of schizophrenia. We have previously reported enlargements in subcortical brain structure volumes and impairment of neurocognitive functioning as measured by the MATRICS Cognitive Consensus Battery (MCCB) in early onset schizophrenia spectrum disorders (EOS). To our knowledge, no previous study has investigated whether neurocognitive performance and volumetric abnormalities in subcortical brain structures are related in EOS. Methods: Twenty-four patients with EOS and 33 healthy controls (HC) were included in the study. Relationships between the caudate nucleus, the lateral and fourth ventricles volumes and neurocognitive performance were investigated with multivariate linear regression analyses. Intracranial volume, age, antipsychotic medication and IQ were included as independent predictor-variables. Results: The caudate volume was negatively correlated with verbal learning performance uniquely in the EOS group (r=-.454, p = .034). There were comparable positive correlations between the lateral ventricular volume and the processing speed, attention and reasoning and problem solving domains for both the EOS patients and the healthy controls. Antipsychotic medication was related to ventricular enlargements, but did not affect the brain structure-function relationship. Conclusion: Enlargement of the caudate volume was related to poorer verbal learning performance in patients with EOS. Despite a 32% enlargement of the lateral ventricles in the EOS group, associations to processing speed, attention and reasoning and problem solving were similar for both the EOS and the HC groups. © 2015 Juuhl-Langseth et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Brain structural abnormalities as well as neurocognitive dysfunction, are found in schizophrenia and in bipolar disorder. Based on the fact that both brain structure and neurocognitive functioning are significantly heritable and affected in both schizophrenia and bipolar disorder, relationships between them are expected. However, previous studies report inconsistent findings. Also, schizophrenia and bipolar disorder are classified as separate disease entities, but demonstrate overlap with regard to symptomatology and genetic liability. Few studies have directly compared brain structure abnormalities or relationships between brain structure and neurocognitive functioning between the diseases and, it remains unclear if findings are similar or different between patients with schizophrenia or bipolar disorder. The aims of the thesis were 1) to characterize brain structure and the relationships with neurocognitive performance in schizophrenia and bipolar disorder and healthy control subjects and, 2) to investigate these characteristics for differences and similarities between the subject groups. Two independent subject samples from two similar ongoing research projects at Karolinska Institutet in Sweden (HUBIN) and at the University of Oslo in Norway (TOP), were included. The participants were patients with schizophrenia or bipolar disorder, and healthy control subjects. All subjects were characterized using magnetic resonance imaging (MRI) of the brain and neuropsychological test methods. Brain cortical thickness and surface area measurements, as well as subcortical structure volumes were obtained using automated computer image analysis methods. Schizophrenia and bipolar disorder type 1 patients demonstrated cortical thinning in overlapping prefrontal and temporo-parietal brain regions compared with healthy controls, and schizophrenia and bipolar disorder patients demonstrated similar findings of subcortical volume abnormalities, compared to healthy controls. The identified abnormalities were more pronounced among schizophrenia patients. Cortical thickness and surface area in predominantly frontal and temporal regions, but also occipital regions, and several of the subcortical structure volumes, were related to neurocognitive performance in both patients and healthy controls. Between-group comparisons showed that some structure/function relationships were specific to schizophrenia and/or bipolar disorder. In conclusion, the results demonstrate numerous similar brain structure abnormalities in schizophrenia and bipolar disorder, consistent with a common underlying pathophysiology. Mostly similar brain structure/function relationships were found between patients and controls. Few relationships were found to be similar in schizophrenia and bipolar disorder, but different from healthy controls. Consequently, our findings do not indicate that the neurocognitive dysfunction found in both schizophrenia and bipolar disorder have common brain structural correlates. Some disease-specific relationships were found between brain structure and neurocognition, possibly reflecting disruptions in brain regions that contribute to specific cognitive functions and, could be of relevance to the pathophysiology in schizophrenia and bipolar disorder.