Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes

Early life environments interact with genotype to determine stable phenotypic outcomes. Here we examined the influence of a variant in the brain-derived neurotropic factor (BDNF) gene (Val66Met), which underlies synaptic plasticity throughout the central nervous system, on the degree to which antena...

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Main Authors: Tuan, Ta Anh, Chen, Li, Pan, Hong, Teh, Ai Ling, MacIsaac, Julia L., Mah, Sarah M., McEwen, Lisa M., Li, Yue, Chen, Helen, Broekman, Birit F. P., Buschdorf, Jan Paul, Chong, Yap Seng, Kwek, Kenneth, Saw, Seang Mei, Gluckman, Peter D., Fortier, Marielle V., Rifkin-Graboi, Anne, Kobor, Michael S., Qiu, Anqi, Meaney, Michael J., Holbrook, Joanna D.
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2016
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Online Access:https://hdl.handle.net/10356/81986
http://hdl.handle.net/10220/41054
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-819862020-03-07T12:18:09Z Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes Tuan, Ta Anh Chen, Li Pan, Hong Teh, Ai Ling MacIsaac, Julia L. Mah, Sarah M. McEwen, Lisa M. Li, Yue Chen, Helen Broekman, Birit F. P. Buschdorf, Jan Paul Chong, Yap Seng Kwek, Kenneth Saw, Seang Mei Gluckman, Peter D. Fortier, Marielle V. Rifkin-Graboi, Anne Kobor, Michael S. Qiu, Anqi Meaney, Michael J. Holbrook, Joanna D. School of Biological Sciences Brain-derived neurotrophic factor (BDNF) Val66met Early life environments interact with genotype to determine stable phenotypic outcomes. Here we examined the influence of a variant in the brain-derived neurotropic factor (BDNF) gene (Val66Met), which underlies synaptic plasticity throughout the central nervous system, on the degree to which antenatal maternal anxiety associated with neonatal DNA methylation. We also examined the association between neonatal DNA methylation and brain substructure volume, as a function of BDNF genotype. Infant, but not maternal, BDNF genotype dramatically influences the association of antenatal anxiety on the epigenome at birth as well as that between the epigenome and neonatal brain structure. There was a greater impact of antenatal maternal anxiety on the DNA methylation of infants with the methionine (Met)/Met compared to both Met/valine (Val) and Val/Val genotypes. There were significantly more cytosine–phosphate–guanine sites where methylation levels covaried with right amygdala volume among Met/Met compared with both Met/Val and Val/Val carriers. In contrast, more cytosine–phosphate–guanine sites covaried with left hippocampus volume in Val/Val infants compared with infants of the Met/Val or Met/Met genotype. Thus, antenatal Maternal Anxiety × BDNF Val66Met Polymorphism interactions at the level of the epigenome are reflected differently in the structure of the amygdala and the hippocampus. These findings suggest that BDNF genotype regulates the sensitivity of the methylome to early environment and that differential susceptibility to specific environmental conditions may be both tissue and function specific. NRF (Natl Research Foundation, S’pore) ASTAR (Agency for Sci., Tech. and Research, S’pore) NMRC (Natl Medical Research Council, S’pore) 2016-08-03T08:53:43Z 2019-12-06T14:44:17Z 2016-08-03T08:53:43Z 2019-12-06T14:44:17Z 2015 Journal Article Chen, L., Pan, H., Tuan, T. A., Teh, A. L., MacIsaac, J. L., Mah, S. M., et al. (2015). Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes. Development and Psychopathology, 27(1), 137-150. https://hdl.handle.net/10356/81986 http://hdl.handle.net/10220/41054 10.1017/S0954579414001357 en Development and Psychopathology © 2015 Cambridge University Press.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Brain-derived neurotrophic factor (BDNF)
Val66met
spellingShingle Brain-derived neurotrophic factor (BDNF)
Val66met
Tuan, Ta Anh
Chen, Li
Pan, Hong
Teh, Ai Ling
MacIsaac, Julia L.
Mah, Sarah M.
McEwen, Lisa M.
Li, Yue
Chen, Helen
Broekman, Birit F. P.
Buschdorf, Jan Paul
Chong, Yap Seng
Kwek, Kenneth
Saw, Seang Mei
Gluckman, Peter D.
Fortier, Marielle V.
Rifkin-Graboi, Anne
Kobor, Michael S.
Qiu, Anqi
Meaney, Michael J.
Holbrook, Joanna D.
Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes
description Early life environments interact with genotype to determine stable phenotypic outcomes. Here we examined the influence of a variant in the brain-derived neurotropic factor (BDNF) gene (Val66Met), which underlies synaptic plasticity throughout the central nervous system, on the degree to which antenatal maternal anxiety associated with neonatal DNA methylation. We also examined the association between neonatal DNA methylation and brain substructure volume, as a function of BDNF genotype. Infant, but not maternal, BDNF genotype dramatically influences the association of antenatal anxiety on the epigenome at birth as well as that between the epigenome and neonatal brain structure. There was a greater impact of antenatal maternal anxiety on the DNA methylation of infants with the methionine (Met)/Met compared to both Met/valine (Val) and Val/Val genotypes. There were significantly more cytosine–phosphate–guanine sites where methylation levels covaried with right amygdala volume among Met/Met compared with both Met/Val and Val/Val carriers. In contrast, more cytosine–phosphate–guanine sites covaried with left hippocampus volume in Val/Val infants compared with infants of the Met/Val or Met/Met genotype. Thus, antenatal Maternal Anxiety × BDNF Val66Met Polymorphism interactions at the level of the epigenome are reflected differently in the structure of the amygdala and the hippocampus. These findings suggest that BDNF genotype regulates the sensitivity of the methylome to early environment and that differential susceptibility to specific environmental conditions may be both tissue and function specific.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Tuan, Ta Anh
Chen, Li
Pan, Hong
Teh, Ai Ling
MacIsaac, Julia L.
Mah, Sarah M.
McEwen, Lisa M.
Li, Yue
Chen, Helen
Broekman, Birit F. P.
Buschdorf, Jan Paul
Chong, Yap Seng
Kwek, Kenneth
Saw, Seang Mei
Gluckman, Peter D.
Fortier, Marielle V.
Rifkin-Graboi, Anne
Kobor, Michael S.
Qiu, Anqi
Meaney, Michael J.
Holbrook, Joanna D.
format Article
author Tuan, Ta Anh
Chen, Li
Pan, Hong
Teh, Ai Ling
MacIsaac, Julia L.
Mah, Sarah M.
McEwen, Lisa M.
Li, Yue
Chen, Helen
Broekman, Birit F. P.
Buschdorf, Jan Paul
Chong, Yap Seng
Kwek, Kenneth
Saw, Seang Mei
Gluckman, Peter D.
Fortier, Marielle V.
Rifkin-Graboi, Anne
Kobor, Michael S.
Qiu, Anqi
Meaney, Michael J.
Holbrook, Joanna D.
author_sort Tuan, Ta Anh
title Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes
title_short Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes
title_full Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes
title_fullStr Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes
title_full_unstemmed Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes
title_sort brain-derived neurotrophic factor (bdnf) val66met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes
publishDate 2016
url https://hdl.handle.net/10356/81986
http://hdl.handle.net/10220/41054
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