TY - JOUR
T1 - RELN rs7341475 Associates with Brain Structure in Japanese Healthy Females
AU - Yamaguchi, Ryo
AU - Matsudaira, Izumi
AU - Takeuchi, Hikaru
AU - Imanishi, Tadashi
AU - Kimura, Ryosuke
AU - Tomita, Hiroaki
AU - Kawashima, Ryuta
AU - Taki, Yasuyuki
N1 - Funding Information:
We thank Shuzo Yamamoto, Yasuko Tatewaki, Takamitsu Shinada, and all the staff and team members for helping with this study and acknowledge the contribution of all the study participants. We would also like to thank Riken Genesis Co. Ltd. for SNP typing some of the subjects and Editage ( www.editage.jp) for English language editing. R. Yamaguchi and I. Matsudaira designed this study; H. Takeuchi and I. Matsudaira collected the data; H. Tomita, T. Imanishi, and R. Kimura analyzed the genetic data. R. Yamaguchi processed brain images and performed the statistical analysis. R. Kawashima, H. Takeuchi, Y. Taki, and I. Matsudaira acquired funding. Y. Taki supervised this study. R. Yamaguchi and I. Matsudaira wrote and edited the paper. All authors read and approved the final version of the manuscript. None. This study was 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), a Grant-in-Aid for Scientific Research (B) (KAKENHI 19H04211), a Grant-in-Aid for Scientific Research (B) (KAKENHI 19H03893), a Grant-in-Aid for Scientific Research (A) (KAKENHI 16H01752), a Grant-in-Aid for JSPS fellows (KAKENHI 17J02379) from the Ministry of Education, Culture, Sports, Science, and Technology, and a Grant-in-Aid of Tohoku University, Division for Interdisciplinary Advanced Research and Education.
Funding Information:
This study was 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), a Grant-in-Aid for Scientific Research (B) (KAKENHI 19H04211), a Grant-in-Aid for Scientific Research (B) (KAKENHI 19H03893), a Grant-in-Aid for Scientific Research (A) (KAKENHI 16H01752), a Grant-in-Aid for JSPS fellows (KAKENHI 17J02379) from the Ministry of Education, Culture, Sports, Science, and Technology, and a Grant-in-Aid of Tohoku University, Division for Interdisciplinary Advanced Research and Education.
Publisher Copyright:
© 2022 IBRO
PY - 2022/7/1
Y1 - 2022/7/1
N2 - Although temperament has been regarded as an innate aspect of human personality, its association with proteins involved in embryonic development is unclear. Reelin, encoded by RELN, plays an important role in brain development. Herein, we investigated the association between the RELN rs7341475 (G/A) single nucleotide polymorphism, detected as a female-specific risk factor for schizophrenia, brain structure, and temperament to elucidate the role of RELN in the development of human personality. In this study, 1580 healthy young Japanese adults were genotyped for RELN rs7341475 and completed the Temperament and Character Inventory. Whole-brain analysis of covariance was conducted to investigate differences between genotypes in regional gray matter volume (rGMV) and cortical morphology. Additionally, multiple regression analysis was performed to examine the association of four temperaments with rGMV. Those statistical analyses were performed separately for males and females. Individuals with G/G homozygosity showed significantly greater rGMV in several areas of the brain, particularly the bilateral cingulate and temporal gyrus, as well as a larger value of fractal dimension in the left lateral occipital cortex. Furthermore, of the four temperaments, the novelty seeking was significantly and positively associated with rGMV in the right superior temporal gyrus, partially overlapping with areas where differences between the rs7341475 genotypes were detected. The above findings were detected only in females, but not in males. This is the first study to demonstrate the contribution of RELN rs7341475 to differences in brain structure in Japanese females, which may indicate vulnerability to schizophrenia and variations in human personality.
AB - Although temperament has been regarded as an innate aspect of human personality, its association with proteins involved in embryonic development is unclear. Reelin, encoded by RELN, plays an important role in brain development. Herein, we investigated the association between the RELN rs7341475 (G/A) single nucleotide polymorphism, detected as a female-specific risk factor for schizophrenia, brain structure, and temperament to elucidate the role of RELN in the development of human personality. In this study, 1580 healthy young Japanese adults were genotyped for RELN rs7341475 and completed the Temperament and Character Inventory. Whole-brain analysis of covariance was conducted to investigate differences between genotypes in regional gray matter volume (rGMV) and cortical morphology. Additionally, multiple regression analysis was performed to examine the association of four temperaments with rGMV. Those statistical analyses were performed separately for males and females. Individuals with G/G homozygosity showed significantly greater rGMV in several areas of the brain, particularly the bilateral cingulate and temporal gyrus, as well as a larger value of fractal dimension in the left lateral occipital cortex. Furthermore, of the four temperaments, the novelty seeking was significantly and positively associated with rGMV in the right superior temporal gyrus, partially overlapping with areas where differences between the rs7341475 genotypes were detected. The above findings were detected only in females, but not in males. This is the first study to demonstrate the contribution of RELN rs7341475 to differences in brain structure in Japanese females, which may indicate vulnerability to schizophrenia and variations in human personality.
KW - RELN
KW - cortical morphology
KW - gray matter
KW - schizophrenia
KW - single nucleotide polymorphism
KW - temperament
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UR - http://www.scopus.com/inward/citedby.url?scp=85133102575&partnerID=8YFLogxK
U2 - 10.1016/j.neuroscience.2022.05.007
DO - 10.1016/j.neuroscience.2022.05.007
M3 - Article
C2 - 35569645
AN - SCOPUS:85133102575
SN - 0306-4522
VL - 494
SP - 38
EP - 50
JO - Neuroscience
JF - Neuroscience
ER -