4.5 Article

Aberrant default mode connectivity in adolescents with early-onset psychosis: A resting state fMRI study

期刊

NEUROIMAGE-CLINICAL
卷 33, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2021.102881

关键词

Early-onset psychosis (EOP); Schizophrenia; Affective psychosis; Default mode network (DMN); Resting state fMRI (rsfMRI); Independent component analysis (ICA)

资金

  1. Research Council of Norway [223273, 213700, 250358]
  2. South-Eastern Norway Regional Health Authority [2019107, 2020086, 2019099, 2020020]
  3. Swedish Research Council [2017-00949]
  4. FORTE 2012
  5. Swedish Research Council [2017-00949] Funding Source: Swedish Research Council

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The study revealed significantly reduced DMN connectivity in adolescent patients with early onset psychosis compared to healthy controls, with the subgroup analysis showing strongest deviations for affective psychosis, followed by other psychotic disorders and schizophrenia. There was no association found between DMN connectivity strength and current use of psychotropic medication.
Abnormal default mode network (DMN) connectivity has been found in schizophrenia and other psychotic disorders. However, there are limited studies on early onset psychosis (EOP), and their results show lack of agreement. Here, we investigated within-network DMN connectivity in EOP compared to healthy controls (HC), and its relationship to clinical characteristics. A sample of 68 adolescent patients with EOP (mean age 16.53 +/- 1.12 [SD] years, females 66%) and 95 HC (mean age 16.24 +/- 1.50 [SD], females 60%) from two Scandinavian cohorts underwent resting state functional magnetic resonance imaging (rsfMRI). A group independent component analysis (ICA) was performed to identify the DMN across all participants. Dual regression was used to estimate spatial maps reflecting each participant's DMN network, which were compared between EOP and HC using voxel-wise general linear models and permutation-based analyses. Subgroup analyses were performed within the patient group, to explore associations between diagnostic subcategories and current use of psychotropic medication in relation to connectivity strength. The analysis revealed significantly reduced DMN connectivity in EOP compared to HC in the posterior cingulate cortex, precuneus, fusiform cortex, putamen, pallidum, amygdala, and insula. The subgroup analysis in the EOP group showed strongest deviations for affective psychosis, followed by other psychotic disorders and schizophrenia. There was no association between DMN connectivity strength and the current use of psychotropic medication. In conclusion, the findings demonstrate weaker DMN connectivity in adolescent patients with EOP compared to healthy peers, and differential effects across diagnostic subcategories, which may inform our understanding of underlying disease mechanisms in EOP.

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