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dc.contributor.authorSaricicek, Aybala
dc.contributor.authorYalin, Nefize
dc.contributor.authorHidiroglu, Ceren
dc.contributor.authorCavusoglu, Berrin
dc.contributor.authorTas, Cumhur
dc.contributor.authorCeylan, Deniz
dc.contributor.authorOzerdem, Aysegul
dc.date.accessioned2021-11-09T19:50:13Z
dc.date.available2021-11-09T19:50:13Z
dc.date.issued2015
dc.identifier.issn0165-0327
dc.identifier.issn1573-2517
dc.identifier.urihttps://doi.org/10.1016/j.jad.2015.06.055
dc.identifier.urihttps://hdl.handle.net/20.500.12440/4218
dc.description.abstractBackground: Bipolar disorder (BD) is a highly heritable mental illness which is associated with neuroanatomical abnormalities. Investigating healthy individuals at high genetic risk for bipolar disorder may help to identify neuroanatomical markers of risk and resilience without the confounding effects of burden of illness or medication. Methods: Structural magnetic resonance imaging scans were acquired from 30 euthymic patients with BD-1 (BP), 28 healthy first degree relatives of BD-I patients (HR), and 30 healthy controls (HC). Data was analyzed using DARTEL for voxel based morphometry in SPM8. Results: Whole-brain analysis revealed a significant main effect of group in the gray matter volume in bilateral inferior frontal gyrus, left parahippocampal gyrus, left lingual gyrus and cerebellum, posterior cingulate gyrus, and supramarginal gyrus (alphasim corrected (<= 0.05 FWE)). Post-hoc t-tests showed that inferior frontal gyrus volumes were bilaterally larger both in BP and HR than in HC. BP and HR also had smaller cerebellar volume compared with HC. In addition, BP had smaller left lingual gyms volume, whereas HR had larger left parahippocampal and supramarginal gyms volume compared with HC. Limitations: This study was cross-sectional and the sample size was not large. All bipolar patients were on medication, therefore we were not able to exclude medication effects in bipolar group in this study. Conclusions: Our findings suggest that increased inferior frontal gyms and decreased cerebellar volumes might be associated with genetic predisposition for bipolar disorder. Longitudinal studies are needed to better understand the predictive and prognostic value of structural changes in these regions. (C) 2015 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipDokuz Eylul University Department of Scientific Research Projects FundingDokuz Eylul University [2012.KB.SAG.062]en_US
dc.description.sponsorshipThis work was supported by the Dokuz Eylul University Department of Scientific Research Projects Funding (Project no.: 2012.KB.SAG.062). Funding source has no role in study design; in the collection, analysis and interpretation of data; in the writing of the report; and in the decision to submit the article for publication.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.ispartofJournal of Affective Disordersen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBipolar disorderen_US
dc.subjectVoxel based morphometryen_US
dc.subjectEndophenotypeen_US
dc.subjectInferior frontal gyrusen_US
dc.subjectCerebellumen_US
dc.titleNeuroanatomical correlates of genetic risk for bipolar disorder: A voxel-based morphometry study in bipolar type I patients and healthy first degree relativesen_US
dc.typearticleen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.description.wospublicationidWOS:000360966400017en_US
dc.departmentGümüşhane Üniversitesien_US
dc.authoridCeylan, Deniz / 0000-0002-1438-8240
dc.authoridAydogan, Aybala Saricicek / 0000-0002-8962-7269
dc.identifier.volume186en_US
dc.identifier.startpage110en_US
dc.identifier.doi10.1016/j.jad.2015.06.055
dc.identifier.endpage118en_US
dc.authorwosidada, emel / AAC-3966-2020
dc.authorwosidCeylan, Deniz / E-9415-2017
dc.authorwosidAydogan, Aybala Saricicek / AAU-9716-2021
dc.authorwosidAda, Emel / AAR-7664-2020
dc.description.pubmedpublicationidPubMed: 26233321en_US


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