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- Publisher Website: 10.1016/j.neuroimage.2008.05.025
- Scopus: eid_2-s2.0-47949131223
- PMID: 18585932
- WOS: WOS:000258695200036
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Article: The effects of neuregulin1 on brain function in controls and patients with schizophrenia and bipolar disorder
Title | The effects of neuregulin1 on brain function in controls and patients with schizophrenia and bipolar disorder | ||||||
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Authors | |||||||
Keywords | Bipolar disorder Functional magnetic resonance imaging Genetics Neuregulin1 Schizophrenia Verbal fluency | ||||||
Issue Date | 2008 | ||||||
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ynimg | ||||||
Citation | Neuroimage, 2008, v. 42 n. 2, p. 817-826 How to Cite? | ||||||
Abstract | Recent studies have identified neuregulin1 as a probable susceptibility gene for schizophrenia and bipolar disorder. However, little is known about how this gene may affect brain function to increase vulnerability to these disorders. The present investigation examined the impact of neuregulin1 genotype on brain function in patients with schizophrenia, patients with bipolar I disorder and healthy volunteers. We used functional magnetic resonance imaging to measure brain responses during a verbal fluency task in a total of 115 subjects comprising 41 patients with schizophrenia, 29 patients with bipolar disorder and 45 healthy volunteers. We then used statistical parametric mapping to estimate the main effects of diagnostic group, the main effect of genotype and their interaction. We tested the hypothesis that the high-risk variant of neuregulin1 would be associated with altered prefrontal function. In all three diagnostic groups, the high-risk variant of neuregulin1 was associated with greater deactivation in the left precuneus. In addition, there was an interaction between diagnosis and genotype in two regions of the prefrontal cortex. The right inferior frontal gyrus expressed increased activation in individuals with the high-risk variant, but only in patients with schizophrenia. Conversely, the right posterior orbital gyrus expressed increased activation in individuals with the high-risk variant, but only in patients with bipolar disorder. Our results suggest that genetic variation in neuregulin1 has a measurable impact on brain function and provide preliminary evidence for a disease-specific pattern of gene action in different regions of the prefrontal cortex. © 2008 Elsevier Inc. All rights reserved. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/141845 | ||||||
ISSN | 2023 Impact Factor: 4.7 2023 SCImago Journal Rankings: 2.436 | ||||||
ISI Accession Number ID |
Funding Information: AM is funded by the Higher Education Funding Council for England (HEFCE). CF was funded by a Wellcome Trust Fellowship. | ||||||
References |
DC Field | Value | Language |
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dc.contributor.author | Mechelli, A | en_HK |
dc.contributor.author | Prata, DP | en_HK |
dc.contributor.author | Fu, CHY | en_HK |
dc.contributor.author | Picchioni, M | en_HK |
dc.contributor.author | Kane, F | en_HK |
dc.contributor.author | Kalidindi, S | en_HK |
dc.contributor.author | McDonald, C | en_HK |
dc.contributor.author | Demjaha, A | en_HK |
dc.contributor.author | Kravariti, E | en_HK |
dc.contributor.author | Toulopoulou, T | en_HK |
dc.contributor.author | Murray, R | en_HK |
dc.contributor.author | Collier, DA | en_HK |
dc.contributor.author | McGuire, PK | en_HK |
dc.date.accessioned | 2011-09-27T03:03:10Z | - |
dc.date.available | 2011-09-27T03:03:10Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Neuroimage, 2008, v. 42 n. 2, p. 817-826 | en_HK |
dc.identifier.issn | 1053-8119 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/141845 | - |
dc.description.abstract | Recent studies have identified neuregulin1 as a probable susceptibility gene for schizophrenia and bipolar disorder. However, little is known about how this gene may affect brain function to increase vulnerability to these disorders. The present investigation examined the impact of neuregulin1 genotype on brain function in patients with schizophrenia, patients with bipolar I disorder and healthy volunteers. We used functional magnetic resonance imaging to measure brain responses during a verbal fluency task in a total of 115 subjects comprising 41 patients with schizophrenia, 29 patients with bipolar disorder and 45 healthy volunteers. We then used statistical parametric mapping to estimate the main effects of diagnostic group, the main effect of genotype and their interaction. We tested the hypothesis that the high-risk variant of neuregulin1 would be associated with altered prefrontal function. In all three diagnostic groups, the high-risk variant of neuregulin1 was associated with greater deactivation in the left precuneus. In addition, there was an interaction between diagnosis and genotype in two regions of the prefrontal cortex. The right inferior frontal gyrus expressed increased activation in individuals with the high-risk variant, but only in patients with schizophrenia. Conversely, the right posterior orbital gyrus expressed increased activation in individuals with the high-risk variant, but only in patients with bipolar disorder. Our results suggest that genetic variation in neuregulin1 has a measurable impact on brain function and provide preliminary evidence for a disease-specific pattern of gene action in different regions of the prefrontal cortex. © 2008 Elsevier Inc. All rights reserved. | en_HK |
dc.language | eng | en_US |
dc.publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ynimg | en_HK |
dc.relation.ispartof | NeuroImage | en_HK |
dc.subject | Bipolar disorder | en_HK |
dc.subject | Functional magnetic resonance imaging | en_HK |
dc.subject | Genetics | en_HK |
dc.subject | Neuregulin1 | en_HK |
dc.subject | Schizophrenia | en_HK |
dc.subject | Verbal fluency | en_HK |
dc.title | The effects of neuregulin1 on brain function in controls and patients with schizophrenia and bipolar disorder | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Toulopoulou, T:timothea@hku.hk | en_HK |
dc.identifier.authority | Toulopoulou, T=rp01542 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.neuroimage.2008.05.025 | en_HK |
dc.identifier.pmid | 18585932 | - |
dc.identifier.scopus | eid_2-s2.0-47949131223 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-47949131223&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 42 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 817 | en_HK |
dc.identifier.epage | 826 | en_HK |
dc.identifier.isi | WOS:000258695200036 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Mechelli, A=6603693131 | en_HK |
dc.identifier.scopusauthorid | Prata, DP=14632352500 | en_HK |
dc.identifier.scopusauthorid | Fu, CHY=8502155300 | en_HK |
dc.identifier.scopusauthorid | Picchioni, M=6507443795 | en_HK |
dc.identifier.scopusauthorid | Kane, F=24829114900 | en_HK |
dc.identifier.scopusauthorid | Kalidindi, S=24366595400 | en_HK |
dc.identifier.scopusauthorid | McDonald, C=8749594800 | en_HK |
dc.identifier.scopusauthorid | Demjaha, A=23970361800 | en_HK |
dc.identifier.scopusauthorid | Kravariti, E=8855469000 | en_HK |
dc.identifier.scopusauthorid | Toulopoulou, T=8855468700 | en_HK |
dc.identifier.scopusauthorid | Murray, R=35406239400 | en_HK |
dc.identifier.scopusauthorid | Collier, DA=26642980600 | en_HK |
dc.identifier.scopusauthorid | McGuire, PK=7101880438 | en_HK |
dc.identifier.citeulike | 3432720 | - |
dc.identifier.issnl | 1053-8119 | - |