TY - JOUR
T1 - Association Between OLIG2 Gene SNP rs1059004 and Negative Self-Schema Constructing Trait Factors Underlying Susceptibility to Depression
AU - Komatsu, Hiroshi
AU - Takeuchi, Hikaru
AU - Ono, Chiaki
AU - Yu, Zhiqian
AU - Kikuchi, Yoshie
AU - Kakuto, Yoshihisa
AU - Funakoshi, Shunichi
AU - Ono, Takashi
AU - Kawashima, Ryuta
AU - Taki, Yasuyuki
AU - Tomita, Hiroaki
N1 - Funding Information:
This work was partially supported by a grant-in-aid for scientific research on innovative areas (No. 24116007) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan and the Strategic Research Program for Brain Sciences from the Japan Agency for Medical Research and Development, AMED (JP20dm0107099). This study was also partially supported by JST/RISTEX, JST/CREST, a grant-in-aid for young scientists (B) (KAKENHI 23700306), a grant-in-aid for young scientists (A) (KAKENHI 25700012), and Tohoku University Advanced Research Center for Innovations in Next-Generation Medicine, Japan. None of the funding sources mentioned above were involved in the study design; collection, analysis, or interpretation of data; writing of the report, or decision to submit the article for publication.
Funding Information:
We thank Haruka Nouchi for conducting the psychological tests, all other assistants for helping with the experiments in the study, and the study participants and all our other colleagues at Tohoku University for their support. Funding. This work was partially supported by a grant-in-aid for scientific research on innovative areas (No. 24116007) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan and the Strategic Research Program for Brain Sciences from the Japan Agency for Medical Research and Development, AMED (JP20dm0107099). This study was also partially supported by JST/RISTEX, JST/CREST, a grant-in-aid for young scientists (B) (KAKENHI 23700306), a grant-in-aid for young scientists (A) (KAKENHI 25700012), and Tohoku University Advanced Research Center for Innovations in Next-Generation Medicine, Japan. None of the funding sources mentioned above were involved in the study design; collection, analysis, or interpretation of data; writing of the report, or decision to submit the article for publication.
Publisher Copyright:
© Copyright © 2021 Komatsu, Takeuchi, Ono, Yu, Kikuchi, Kakuto, Funakoshi, Ono, Kawashima, Taki and Tomita.
PY - 2021/3/8
Y1 - 2021/3/8
N2 - 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.
AB - 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.
KW - depressive symptoms
KW - negative self-schema
KW - OLIG2
KW - oligodendrocyte
KW - single nucleotide polymorphism
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U2 - 10.3389/fpsyt.2021.631475
DO - 10.3389/fpsyt.2021.631475
M3 - Article
AN - SCOPUS:85103058683
SN - 1664-0640
VL - 12
JO - Frontiers in Psychiatry
JF - Frontiers in Psychiatry
M1 - 631475
ER -