Neuroimaging alterations and relapse in early-stage psychosis
Marina M. MihaljeviciD, Anisha NagpaliD, Semra EtyemeziD, Zui C. NaritaiD, Anna Ross, Rebecca Schaub, Nicola G. CascellaiD, Jennifer Marie CoughliniD, Gerald NestadtiD, Frederik C. Nucifora, Thomas W. SedlakiD, Koko Ishizuka, Vince D. CalhouniD, Andreia Vasconcellos FariaiD, Kun Yang, Akira SawaiD
Abstract
Recent reports have indicated that the occurrence of symptom exacerbation in early-stage psychosis could result in brain changes. Such a symptom exacerbation is frequently called relapse, which underlies a poorer disease outcome. Thus, it is important to identify neuroimaging alterations that are specifically seen in patients who experience relapse in early-stage psychosis. We hypothesized that this specific patient group may be more homogenous in disease-associated signatures likely to be linked to relapse, compared with the overall patient group. Such sub-stratified patient group and neuroimaging signatures would be useful for the biological understanding of relapse. To address this goal, we conducted a cross-sectional study (85 patients with early-stage psychosis and 94 healthy controls) with the use of medical records in a retrospective manner. To define the specific sub-group with the past experience of relapse, we used hospitalization due to psychotic symptom exacerbation, according to many publications that used this factor as a proxy for relapse. By examining resting-state functional connectivity (FC) for the study subjects, we validated our hypothesis and defined 131 FCs possibly associated with relapse. Through these studies, 3 brain regions (the thalamus, precentral gyrus, and dorsal anterior cingulate cortex) were underscored.
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