Please use this identifier to cite or link to this item: https://doi.org/10.1017/S0033291716001410
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dc.titleDisrupted salience network functional connectivity and white-matter microstructure in persons at risk for psychosis: findings from the LYRIKS study
dc.contributor.authorWang, C
dc.contributor.authorJi, F
dc.contributor.authorHong, Z
dc.contributor.authorPoh, JS
dc.contributor.authorKrishnan, R
dc.contributor.authorLee, J
dc.contributor.authorRekhi, G
dc.contributor.authorKeefe, RSE
dc.contributor.authorAdcock, RA
dc.contributor.authorWood, SJ
dc.contributor.authorFornito, A
dc.contributor.authorPasternak, O
dc.contributor.authorChee, MWL
dc.contributor.authorZhou, J
dc.date.accessioned2021-11-15T01:19:15Z
dc.date.available2021-11-15T01:19:15Z
dc.date.issued2016-10-01
dc.identifier.citationWang, C, Ji, F, Hong, Z, Poh, JS, Krishnan, R, Lee, J, Rekhi, G, Keefe, RSE, Adcock, RA, Wood, SJ, Fornito, A, Pasternak, O, Chee, MWL, Zhou, J (2016-10-01). Disrupted salience network functional connectivity and white-matter microstructure in persons at risk for psychosis: findings from the LYRIKS study. PSYCHOLOGICAL MEDICINE 46 (13) : 2771-2783. ScholarBank@NUS Repository. https://doi.org/10.1017/S0033291716001410
dc.identifier.issn00332917
dc.identifier.issn14698978
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/206098
dc.description.abstractBackground Salience network (SN) dysconnectivity has been hypothesized to contribute to schizophrenia. Nevertheless, little is known about the functional and structural dysconnectivity of SN in subjects at risk for psychosis. We hypothesized that SN functional and structural connectivity would be disrupted in subjects with At-Risk Mental State (ARMS) and would be associated with symptom severity and disease progression. Method We examined 87 ARMS and 37 healthy participants using both resting-state functional magnetic resonance imaging and diffusion tensor imaging. Group differences in SN functional and structural connectivity were examined using a seed-based approach and tract-based spatial statistics. Subject-level functional connectivity measures and diffusion indices of disrupted regions were correlated with CAARMS scores and compared between ARMS with and without transition to psychosis. Results ARMS subjects exhibited reduced functional connectivity between the left ventral anterior insula and other SN regions. Reduced fractional anisotropy (FA) and axial diffusivity were also found along white-matter tracts in close proximity to regions of disrupted functional connectivity, including frontal-striatal-thalamic circuits and the cingulum. FA measures extracted from these disrupted white-matter regions correlated with individual symptom severity in the ARMS group. Furthermore, functional connectivity between the bilateral insula and FA at the forceps minor were further reduced in subjects who transitioned to psychosis after 2 years. Conclusions Our findings support the insular dysconnectivity of the proximal SN hypothesis in the early stages of psychosis. Further developed, the combined structural and functional SN assays may inform the prognosis of persons at-risk for psychosis.
dc.language.isoen
dc.publisherCAMBRIDGE UNIV PRESS
dc.sourceElements
dc.subjectSocial Sciences
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectPsychology, Clinical
dc.subjectPsychiatry
dc.subjectPsychology
dc.subjectAt risk for psychosis
dc.subjectfunctional connectivity
dc.subjectLYRIKS
dc.subjectsalience network
dc.subjecttransition to psychosis
dc.subjectwhite-matter microstructure
dc.subjectEARLY-ONSET SCHIZOPHRENIA
dc.subjectCLINICAL HIGH-RISK
dc.subjectULTRA-HIGH-RISK
dc.subject1ST EPISODE SCHIZOPHRENIA
dc.subjectRESTING-STATE FMRI
dc.subjectDIFFUSION TENSOR
dc.subjectALZHEIMERS-DISEASE
dc.subjectDEFAULT-MODE
dc.subjectFRONTOTEMPORAL DEMENTIA
dc.subjectSPATIAL STATISTICS
dc.typeArticle
dc.date.updated2021-11-10T08:08:38Z
dc.contributor.departmentMEDICINE
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.contributor.departmentDUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
dc.description.doi10.1017/S0033291716001410
dc.description.sourcetitlePSYCHOLOGICAL MEDICINE
dc.description.volume46
dc.description.issue13
dc.description.page2771-2783
dc.published.statePublished
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