Title Information
Title
BDNF Val66Met Polymorphism and Gonadal Hormones Modulate Basal and Working Memory-Related Neural Functions in Humans
Name: Personal
Name Part
Wei, Shau-Ming NMN
Role
Role Term: Text
creator
Origin Information
Copyright Date
2013
Physical Description
Extent
13, 87 p.
digitalOrigin
born digital
Note
Thesis (Ph.D. -- Brown University (2013)
Name: Personal
Name Part
Berman, Karen
Role
Role Term: Text
Director
Name: Personal
Name Part
Schmidt, Peter
Role
Role Term: Text
Reader
Name: Personal
Name Part
Burwell, Rebecca
Role
Role Term: Text
Reader
Name: Personal
Name Part
Smith, Gwenn
Role
Role Term: Text
Reader
Name: Corporate
Name Part
Brown University. Neuroscience
Role
Role Term: Text
sponsor
Genre (aat)
theses
Subject
Topic
BDNF
Subject
Topic
ovarian steroids
Subject
Topic
PET
Subject
Topic
rest
Subject
Topic
working memory
Subject (FAST) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/915624")
Topic
Estradiol
Subject (FAST) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/1078645")
Topic
Progesterone
Subject (FAST) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/1117483")
Topic
Short-term memory
Record Information
Record Content Source (marcorg)
RPB
Record Creation Date (encoding="iso8601")
20131219
Language
Language Term: Code (ISO639-2B)
eng
Language Term: Text
English
Abstract
Ovarian steroids have been shown to modulate cognitive functions in both animals and humans, but results are inconsistent. The variability of the findings suggests that the response to ovarian hormones may be modulated by a number of yet-to-be identified contextual factors. In this thesis, I demonstrate that brain derived neurotrophic factor (BDNF) and ovarian hormones interactively affect human brain function. <br/> In the absence of direct in vivo measures of BDNF in human brain, the functional BDNF Val66Met polymorphism offers a window on how BDNF influences human cognition. Using positron emission tomography (PET) to study healthy subjects genotyped for the BDNF Val66Met SNP, I found that, compared to Val homozygotes, Met carriers had higher resting regional cerebral blood flow (rCBF) in prefrontal and hippocampal/parahippocampal areas. Moreover, there were significant sex-by-genotype interactions in these regions: Val homozygotes had higher rCBF in females than males, whereas Met carriers showed the opposite relationship. Functional correlations of BA25, hippocampus, and parahippocampus with frontal and temporal networks were positive for Val homozygotes, but negative for Met carriers. In addition, sex-by-genotype analysis of functional connectivity revealed that genotype affected the direction of the interregional correlations differently in men than women. These results demonstrate that BDNF allelic variation and sex interactively affect basal prefrontal and hippocampal function as well as functional connectivity between these regions.<br/> Next, to determine whether the observed sex-by-genotype interaction is mediated by ovarian steroids, I used PET in concert with a six-month hormone manipulation protocol to investigate the interaction between BDNF polymorphism and ovarian steroids, estrogen and progesterone, on working memory-related hippocampal function in healthy women. I demonstrated a hormone-by-genotype interaction in working memory-related hippocampal function that reflected abnormal hippocampal recruitment in Met carriers but only in the presence of estradiol, suggesting a BDNF genotype-mediated sensitivity to ovarian steroids. Collectively, these data emphasize that interpreting the effects of genotype on brain function in women requires knowledge of the ovarian steroid hormone milieu, and that, conversely, it is crucial to consider BDNF genotype when investigating the effects of ovarian steroids.
Identifier: DOI
10.7301/Z0S46Q84
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In Copyright
Access Condition: restriction on access
Collection is open for research.
Type of Resource (primo)
dissertations