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dc.contributor.authorHo, NF
dc.contributor.authorIglesias, JE
dc.contributor.authorSum, MY
dc.contributor.authorKuswanto, CN
dc.contributor.authorSitoh, YY
dc.contributor.authorDe Souza, J
dc.contributor.authorHong, Z
dc.contributor.authorFischl, B
dc.contributor.authorRoffman, JL
dc.contributor.authorZhou, J
dc.contributor.authorSim, K
dc.contributor.authorHolt, DJ
dc.date.accessioned2017-11-22T15:34:08Z
dc.date.available2017-11-22T15:34:08Z
dc.date.issued2017
dc.identifier.citationHo, N.F., Iglesias, J.E., Sum, M.Y., Kuswanto, C., Sitoh, Y.Y., Souza, J., Hong, Z., Fischl, B., Roffman, J., Zhou, J., Sim, K., & Holt, D. (2017). Progression from selective to general involvement of hippocampal subfields in schizophrenia. Molecular Psychiatry, 22, 142–152; doi:10.1038/mp.2016.4es_ES
dc.identifier.issn1359-4184
dc.identifier.urihttp://hdl.handle.net/10810/23638
dc.descriptionPublished online: 23 February 2016es_ES
dc.description.abstractVolume deficits of the hippocampus in schizophrenia have been consistently reported. However, the hippocampus is anatomically heterogeneous; it remains unclear whether certain portions of the hippocampus are affected more than others in schizophrenia. In this study, we aimed to determine whether volume deficits in schizophrenia are confined to specific subfields of the hippocampus and to measure the subfield volume trajectories over the course of the illness. Magnetic resonance imaging scans were obtained from Data set 1: 155 patients with schizophrenia (mean duration of illness of 7 years) and 79 healthy controls, and Data set 2: an independent cohort of 46 schizophrenia patients (mean duration of illness of 18 years) and 46 healthy controls. In addition, follow-up scans were collected for a subset of Data set 1. A novel, automated method based on an atlas constructed from ultra-high resolution, post-mortem hippocampal tissue was used to label seven hippocampal subfields. Significant cross-sectional volume deficits in the CA1, but not of the other subfields, were found in the schizophrenia patients of Data set 1. However, diffuse cross-sectional volume deficits across all subfields were found in the more chronic and ill schizophrenia patients of Data set 2. Consistent with this pattern, the longitudinal analysis of Data set 1 revealed progressive illness-related volume loss (~2–6% per year) that extended beyond CA1 to all of the other subfields. This decline in volume correlated with symptomatic worsening. Overall, these findings provide converging evidence for early atrophy of CA1 in schizophrenia, with extension to other hippocampal subfields and accompanying clinical sequelae over time.es_ES
dc.description.sponsorshipThis study was supported by the National Medical Research Council under the Centre Grant Programme (Institute of Mental Health, Singapore) (NMRC/CG/004/2013) (NFH) and by the National Healthcare Group, Singapore (SIG/05004; SIG/05028), and the Singapore Bioimaging Consortium (RP C-009/2006) research grants awarded to KS, as well grants from the National Institute of Mental Health (DJH: K23MH076054; JLR: K23MH084059) and a Howard Hughes Medical Institute Physician Scientist Early Career Award and grant from Pamlab (JLR). This research was also supported by the Biomedical Research Council, Singapore (awarded to JZ, BMRC 04/1/36/372), the Agency for Science, Technology, and Research (A*STAR) and Duke-NUS Graduate Medical School Signature Research Program funded by Ministry of Health, Singapore.es_ES
dc.language.isoenges_ES
dc.publisherMolecular Psychiatryes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectPrognostic markerses_ES
dc.subjectSchizophreniaes_ES
dc.titleProgression from selective to general involvement of hippocampal subfields in schizophreniaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis work is licensed under a Creative Commons Attribution- NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if thematerial is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http:// creativecommons.org/licenses/by-nc-nd/4.0/es_ES
dc.relation.publisherversionwww.nature.com/mpes_ES
dc.identifier.doi10.1038/mp.2016.4


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