TY - JOUR
T1 - Effect of the interaction between BDNF Val66Met polymorphism and daily physical activity on mean diffusivity
AU - Takeuchi, Hikaru
AU - Tomita, Hiroaki
AU - Taki, Yasuyuki
AU - Kikuchi, Yoshie
AU - Ono, Chiaki
AU - Yu, Zhiqian
AU - Sekiguchi, Atsushi
AU - Nouchi, Rui
AU - Kotozaki, Yuka
AU - Nakagawa, Seishu
AU - Miyauchi, Carlos Makoto
AU - Iizuka, Kunio
AU - Yokoyama, Ryoichi
AU - Shinada, Takamitsu
AU - Yamamoto, Yuki
AU - Hanawa, Sugiko
AU - Araki, Tsuyoshi
AU - Kunitoki, Keiko
AU - Sassa, Yuko
AU - Kawashima, Ryuta
N1 - Publisher Copyright:
© 2019, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2020/6/1
Y1 - 2020/6/1
N2 - Numerous studies have reported that the Met allele of the brain-derived neurotrophic factor (BDNF) gene polymorphism reduces neural plasticity. A reduction in mean diffusivity (MD) in diffusion tensor imaging (DTI) characteristically reflects the neural plasticity that involves increased tissue components. In this study, we revealed that the number of Met-BDNF alleles was negatively associated with MD throughout the whole-brain gray and white matter areas of 743 subjects using DTI and whole-brain multiple regression analyses. Within the same sample, the region of interest analysis revealed that the number of Met-BDNF alleles significantly and positively correlated with the mean FA value in the body of the corpus callosum. In addition, we observed interaction effects between BDNF Val66Met polymorphism and daily physical activity levels on MD, but not FA, in significant clusters of the bilateral hemisphere (n = 577 subjects). Post-hoc multiple regression analyses revealed that after correcting for confounding variables, there was a significant negative correlation between the physical activity level and mean MD of the whole brain in the Val/Val group [standardized partial regression coefficient (β) = −0.196, P = 0.005, t = −2.825], but not in the Val/Met (β = 0.050, P = 0.412, t = 0.822) and Met/Met groups (β = 0.092, P = 0.382, t = 0.878). These results underscore the importance of the interaction between physical activity and the BDNF Val66Met polymorphism, which affects the plasticity of neural mechanisms.
AB - Numerous studies have reported that the Met allele of the brain-derived neurotrophic factor (BDNF) gene polymorphism reduces neural plasticity. A reduction in mean diffusivity (MD) in diffusion tensor imaging (DTI) characteristically reflects the neural plasticity that involves increased tissue components. In this study, we revealed that the number of Met-BDNF alleles was negatively associated with MD throughout the whole-brain gray and white matter areas of 743 subjects using DTI and whole-brain multiple regression analyses. Within the same sample, the region of interest analysis revealed that the number of Met-BDNF alleles significantly and positively correlated with the mean FA value in the body of the corpus callosum. In addition, we observed interaction effects between BDNF Val66Met polymorphism and daily physical activity levels on MD, but not FA, in significant clusters of the bilateral hemisphere (n = 577 subjects). Post-hoc multiple regression analyses revealed that after correcting for confounding variables, there was a significant negative correlation between the physical activity level and mean MD of the whole brain in the Val/Val group [standardized partial regression coefficient (β) = −0.196, P = 0.005, t = −2.825], but not in the Val/Met (β = 0.050, P = 0.412, t = 0.822) and Met/Met groups (β = 0.092, P = 0.382, t = 0.878). These results underscore the importance of the interaction between physical activity and the BDNF Val66Met polymorphism, which affects the plasticity of neural mechanisms.
KW - BDNF
KW - Diffusion tensor imaging
KW - Fractional anisotropy
KW - Mean diffusivity
KW - Neural plasticity
KW - Physical activity
KW - Polymorphism
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U2 - 10.1007/s11682-018-0025-8
DO - 10.1007/s11682-018-0025-8
M3 - Article
C2 - 30617785
AN - SCOPUS:85059684768
SN - 1931-7557
VL - 14
SP - 806
EP - 820
JO - Brain Imaging and Behavior
JF - Brain Imaging and Behavior
IS - 3
ER -