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      Association Between OLIG2 Gene SNP rs1059004 and Negative Self-Schema Constructing Trait Factors Underlying Susceptibility to Depression

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          Abstract

          Recent evidence has indicated that the disruption of oligodendrocytes may be involved in the pathogenesis of depression. Genetic factors are likely to affect trait factors, such as characteristics, rather than state factors, such as depressive symptoms. Previously, a negative self-schema had been proposed as the major characteristic of constructing trait factors underlying susceptibility to depression. Thus, the association between a negative self-schema and the functional single nucleotide polymorphism (SNP) rs1059004 in the OLIG2 gene, which influences OLIG2 gene expression, white matter integrity, and cerebral blood flow, was evaluated. A total of 546 healthy subjects were subjected to genotype and psychological evaluation using the Beck Depression Inventory-II (BDI-II) and the Brief Core Schema Scale (BCSS). The rs1059004 SNP was found to be associated with the self-schema subscales of the BCSS and scores on the BDI-II in an allele dose-dependent manner, and to have a predictive impact on depressive symptoms via a negative-self schema. The results suggest the involvement of a genetic factor regulating oligodendrocyte function in generating a negative-self schema as a trait factor underlying susceptibility to depression.

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              Acute and Longer-Term Outcomes in Depressed Outpatients Requiring One or Several Treatment Steps: A STAR*D Report

              This report describes the participants and compares the acute and longer-term treatment outcomes associated with each of four successive steps in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial.
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                Author and article information

                Contributors
                Journal
                Front Psychiatry
                Front Psychiatry
                Front. Psychiatry
                Frontiers in Psychiatry
                Frontiers Media S.A.
                1664-0640
                08 March 2021
                2021
                : 12
                : 631475
                Affiliations
                [1] 1Department of Psychiatry, Tohoku University Hospital , Sendai, Japan
                [2] 2Miyagi Psychiatric Center , Natori, Japan
                [3] 3Division of Developmental Cognitive Neuroscience, Institute of Development, Aging and Cancer, Tohoku University , Sendai, Japan
                [4] 4Department of Disaster Psychiatry, International Research Institute of Disaster Science, Tohoku University , Sendai, Japan
                [5] 5Department of Community Psychiatry, Tohoku University , Sendai, Japan
                [6] 6Smart Ageing International Research Center, Institute of Development, Aging and Cancer, Tohoku University , Sendai, Japan
                [7] 7Department of Nuclear Medicine and Radiology, Institute of Development, Aging and Cancer, Tohoku University , Sendai, Japan
                [8] 8Division of Medical Neuroimaging Analysis, Department of Community Medical Supports, Tohoku Medical Megabank Organization, Tohoku University , Sendai, Japan
                [9] 9Tohoku Medical Megabank Organization, Tohoku University , Sendai, Japan
                [10] 10Department of Disaster Psychiatry, Graduate School of Medicine, Tohoku University , Sendai, Japan
                [11] 11Department of Psychiatry, Graduate School of Medicine, Tohoku University , Sendai, Japan
                Author notes

                Edited by: Elena Martín-García, Pompeu Fabra University, Spain

                Reviewed by: Shwetal Mehta, Barrow Neurological Institute (BNI), United States; Chuntao Zhao, Cincinnati Children's Hospital Medical Center, United States

                *Correspondence: Hiroshi Komatsu hkomatsu1019@ 123456gmail.com

                This article was submitted to Behavioral and Psychiatric Genetics, a section of the journal Frontiers in Psychiatry

                Article
                10.3389/fpsyt.2021.631475
                7983671
                33762978
                705a2e77-81d7-4540-ae1f-4c8bbedab7ad
                Copyright © 2021 Komatsu, Takeuchi, Ono, Yu, Kikuchi, Kakuto, Funakoshi, Ono, Kawashima, Taki and Tomita.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 20 November 2020
                : 05 February 2021
                Page count
                Figures: 3, Tables: 4, Equations: 0, References: 50, Pages: 10, Words: 7035
                Funding
                Funded by: Ministry of Education, Culture, Sports, Science and Technology 10.13039/501100001700
                Award ID: 23700306
                Award ID: 24116007
                Funded by: Japan Agency for Medical Research and Development 10.13039/100009619
                Categories
                Psychiatry
                Original Research

                Clinical Psychology & Psychiatry
                depressive symptoms,negative self-schema,single nucleotide polymorphism,olig2,oligodendrocyte

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