The BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.

Understanding how genes impact the brain's functional activation for learning and cognition during development remains limited. We asked whether a common genetic variant in the BDNF gene (the Val66Met polymorphism) modulates neural activation in the young brain during a critical period for the...

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Main Authors: Kaja K Jasińska, Peter J Molfese, Sergey A Kornilov, W Einar Mencl, Stephen J Frost, Maria Lee, Kenneth R Pugh, Elena L Grigorenko, Nicole Landi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4995017?pdf=render
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spelling doaj-f22d8ab719ce4611a6e35d3d350d21742020-11-25T02:48:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01118e015744910.1371/journal.pone.0157449The BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.Kaja K JasińskaPeter J MolfeseSergey A KornilovW Einar MenclStephen J FrostMaria LeeKenneth R PughElena L GrigorenkoNicole LandiUnderstanding how genes impact the brain's functional activation for learning and cognition during development remains limited. We asked whether a common genetic variant in the BDNF gene (the Val66Met polymorphism) modulates neural activation in the young brain during a critical period for the emergence and maturation of the neural circuitry for reading. In animal models, the bdnf variation has been shown to be associated with the structure and function of the developing brain and in humans it has been associated with multiple aspects of cognition, particularly memory, which are relevant for the development of skilled reading. Yet, little is known about the impact of the Val66Met polymorphism on functional brain activation in development, either in animal models or in humans. Here, we examined whether the BDNF Val66Met polymorphism (dbSNP rs6265) is associated with children's (age 6-10) neural activation patterns during a reading task (n = 81) using functional magnetic resonance imaging (fMRI), genotyping, and standardized behavioral assessments of cognitive and reading development. Children homozygous for the Val allele at the SNP rs6265 of the BDNF gene outperformed Met allele carriers on reading comprehension and phonological memory, tasks that have a strong memory component. Consistent with these behavioral findings, Met allele carriers showed greater activation in reading-related brain regions including the fusiform gyrus, the left inferior frontal gyrus and left superior temporal gyrus as well as greater activation in the hippocampus during a word and pseudoword reading task. Increased engagement of memory and spoken language regions for Met allele carriers relative to Val/Val homozygotes during reading suggests that Met carriers have to exert greater effort required to retrieve phonological codes.http://europepmc.org/articles/PMC4995017?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kaja K Jasińska
Peter J Molfese
Sergey A Kornilov
W Einar Mencl
Stephen J Frost
Maria Lee
Kenneth R Pugh
Elena L Grigorenko
Nicole Landi
spellingShingle Kaja K Jasińska
Peter J Molfese
Sergey A Kornilov
W Einar Mencl
Stephen J Frost
Maria Lee
Kenneth R Pugh
Elena L Grigorenko
Nicole Landi
The BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.
PLoS ONE
author_facet Kaja K Jasińska
Peter J Molfese
Sergey A Kornilov
W Einar Mencl
Stephen J Frost
Maria Lee
Kenneth R Pugh
Elena L Grigorenko
Nicole Landi
author_sort Kaja K Jasińska
title The BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.
title_short The BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.
title_full The BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.
title_fullStr The BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.
title_full_unstemmed The BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.
title_sort bdnf val66met polymorphism influences reading ability and patterns of neural activation in children.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description Understanding how genes impact the brain's functional activation for learning and cognition during development remains limited. We asked whether a common genetic variant in the BDNF gene (the Val66Met polymorphism) modulates neural activation in the young brain during a critical period for the emergence and maturation of the neural circuitry for reading. In animal models, the bdnf variation has been shown to be associated with the structure and function of the developing brain and in humans it has been associated with multiple aspects of cognition, particularly memory, which are relevant for the development of skilled reading. Yet, little is known about the impact of the Val66Met polymorphism on functional brain activation in development, either in animal models or in humans. Here, we examined whether the BDNF Val66Met polymorphism (dbSNP rs6265) is associated with children's (age 6-10) neural activation patterns during a reading task (n = 81) using functional magnetic resonance imaging (fMRI), genotyping, and standardized behavioral assessments of cognitive and reading development. Children homozygous for the Val allele at the SNP rs6265 of the BDNF gene outperformed Met allele carriers on reading comprehension and phonological memory, tasks that have a strong memory component. Consistent with these behavioral findings, Met allele carriers showed greater activation in reading-related brain regions including the fusiform gyrus, the left inferior frontal gyrus and left superior temporal gyrus as well as greater activation in the hippocampus during a word and pseudoword reading task. Increased engagement of memory and spoken language regions for Met allele carriers relative to Val/Val homozygotes during reading suggests that Met carriers have to exert greater effort required to retrieve phonological codes.
url http://europepmc.org/articles/PMC4995017?pdf=render
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