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Resting-state brain function in schizophrenia and psychotic bipolar probands and their first-degree relatives.

Publication ,  Journal Article
Lui, S; Yao, L; Xiao, Y; Keedy, SK; Reilly, JL; Keefe, RS; Tamminga, CA; Keshavan, MS; Pearlson, GD; Gong, Q; Sweeney, JA
Published in: Psychol Med
January 2015

BACKGROUND: Schizophrenia (SCZ) and psychotic bipolar disorder (PBD) share considerable overlap in clinical features, genetic risk factors and co-occurrence among relatives. The common and unique functional cerebral deficits in these disorders, and in unaffected relatives, remain to be identified. METHOD: A total of 59 healthy controls, 37 SCZ and 57 PBD probands and their unaffected first-degree relatives (38 and 28, respectively) were studied using resting-state functional magnetic resonance imaging (rfMRI). Regional cerebral function was evaluated by measuring the amplitude of low-frequency fluctuations (ALFF). Areas with ALFF alterations were used as seeds in whole-brain functional connectivity analysis. We then tested whether abnormalities identified in probands were present in unaffected relatives. RESULTS: SCZ and PBD probands both demonstrated regional hypoactivity in the orbital frontal cortex and cingulate gyrus, as well as abnormal connectivity within striatal-thalamo-cortical networks. SCZ probands showed greater and more widely distributed ALFF alterations including the thalamus and bilateral parahippocampal gyri. Increased parahippocampal ALFF was related to positive symptoms and cognitive deficit. PBD patients showed uniquely increased functional connectivity between the thalamus and bilateral insula. Only PBD relatives showed abnormal connectivity within striatal-thalamo-cortical networks seen in both proband groups. CONCLUSIONS: The present findings reveal a common pattern of deficits in frontostriatal circuitry across SCZ and PBD, and unique regional and functional connectivity abnormalities that distinguish them. The abnormal network connectivity in PBD relatives that was present in both proband groups may reflect genetic susceptibility associated with risk for psychosis, but within-family associations of this measure were not high.

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Published In

Psychol Med

DOI

EISSN

1469-8978

Publication Date

January 2015

Volume

45

Issue

1

Start / End Page

97 / 108

Location

England

Related Subject Headings

  • Young Adult
  • Schizophrenia
  • Risk Factors
  • Psychiatry
  • Middle Aged
  • Male
  • Magnetic Resonance Imaging
  • Interview, Psychological
  • Humans
  • Genetic Predisposition to Disease
 

Citation

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Lui, S., Yao, L., Xiao, Y., Keedy, S. K., Reilly, J. L., Keefe, R. S., … Sweeney, J. A. (2015). Resting-state brain function in schizophrenia and psychotic bipolar probands and their first-degree relatives. Psychol Med, 45(1), 97–108. https://doi.org/10.1017/S003329171400110X
Lui, S., L. Yao, Y. Xiao, S. K. Keedy, J. L. Reilly, R. S. Keefe, C. A. Tamminga, et al. “Resting-state brain function in schizophrenia and psychotic bipolar probands and their first-degree relatives.Psychol Med 45, no. 1 (January 2015): 97–108. https://doi.org/10.1017/S003329171400110X.
Lui S, Yao L, Xiao Y, Keedy SK, Reilly JL, Keefe RS, et al. Resting-state brain function in schizophrenia and psychotic bipolar probands and their first-degree relatives. Psychol Med. 2015 Jan;45(1):97–108.
Lui, S., et al. “Resting-state brain function in schizophrenia and psychotic bipolar probands and their first-degree relatives.Psychol Med, vol. 45, no. 1, Jan. 2015, pp. 97–108. Pubmed, doi:10.1017/S003329171400110X.
Lui S, Yao L, Xiao Y, Keedy SK, Reilly JL, Keefe RS, Tamminga CA, Keshavan MS, Pearlson GD, Gong Q, Sweeney JA. Resting-state brain function in schizophrenia and psychotic bipolar probands and their first-degree relatives. Psychol Med. 2015 Jan;45(1):97–108.
Journal cover image

Published In

Psychol Med

DOI

EISSN

1469-8978

Publication Date

January 2015

Volume

45

Issue

1

Start / End Page

97 / 108

Location

England

Related Subject Headings

  • Young Adult
  • Schizophrenia
  • Risk Factors
  • Psychiatry
  • Middle Aged
  • Male
  • Magnetic Resonance Imaging
  • Interview, Psychological
  • Humans
  • Genetic Predisposition to Disease