Dissociation of BDNF Val66Met polymorphism on neurocognitive functioning in military veterans with and without a history of remote mild traumatic brain injury.
Dissociation of BDNF Val66Met polymorphism on neurocognitive functioning in military veterans with and without a history of remote mild traumatic brain injury.
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BDNF Val66Met 多态性的分离对有或没有远程轻度创伤性脑损伤史的退伍军人神经认知功能的影响。
DOI:
10.1080/13854046.2020.1740324
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发表时间:
2020
期刊:
影响因子:
--
通讯作者:
Delano-Wood,Lisa
中科院分区:
文献类型:
--
作者:
Merritt,VictoriaC;Clark,AlexandraL;Evangelista,NicoleD;Sorg,ScottF;Schiehser,DawnM;Delano-Wood,Lisa
ObjectiveSince neurocognitive functioning following mild traumatic brain injury (mTBI) may be influenced by genetic factors that mediate synaptic survival and repair, we examined the influence of a common brain-derived neurotrophic factor (BDNF) polymorphism (Val66Met) on cognition using a well-defined sample of military Veterans with and without a history of mTBI.MethodParticipants included 138 Veterans (mTBI = 75; military controls [MCs] = 63) who underwent neuropsychological testing, including completion of self-report measures assessing psychiatric distress, and BDNF genotyping. The mTBI group was tested roughly 66.7 months following their most recent mTBI. Veterans were divided into two groups—Met+ (Met/Met and Met/Val; n = 49) and Met− (Val/Val; n = 89) and compared on domain-specific cognitive composite scores representing memory, executive functioning, and visuospatial speed.ResultsANCOVAs adjusting for psychiatric distress, sex, years of education, and ethnicity/race revealed a significant group (mTBI vs. MC) by BDNF genotype (Met + vs. Met−) interaction for the memory (p= .024; ηp2= .039) and executive functioning (p= .010; ηp2= .050) composites, such that Met+ mTBI Veterans demonstrated better performance than Met− mTBI Veterans on the cognitive measures, whereas Met+ MCs demonstrated worse performance relative to Met− MCs on the cognitive measures. No significant interaction was observed for the visuospatial speed composite (p= .938; ηp2< .001).ConclusionsThese findings offer preliminary evidence to suggest that the Met allele may be protective in the context of remote mTBI. Findings need to be replicated using larger samples, and future studies are necessary to elucidate the precise mechanisms and neural underpinnings of this interaction.