Kennedy Kristen M, Reese Elizabeth D, Horn Marci M, Sizemore April N, Unni Asha K, Meerbrey Michael E, Kalich Allan G, Rodrigue Karen M
Center for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, 1600 Viceroy Dr., Ste 800, Dallas, TX 75235, United States.
Center for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, 1600 Viceroy Dr., Ste 800, Dallas, TX 75235, United States.
Brain Res. 2015 Jul 1;1612:104-17. doi: 10.1016/j.brainres.2014.09.044. Epub 2014 Sep 28.
The BDNF val66met polymorphism (rs6265) influences activity-dependent secretion of brain-derived neurotrophic factor in the synapse, which is crucial for learning and memory. Individuals homozygous or heterozygous for the met allele have lower BDNF secretion than val homozygotes and may be at risk for reduced declarative memory performance, but it remains unclear which types of declarative memory may be affected and how aging of memory across the lifespan is impacted by the BDNF val66met polymorphism. This cross-sectional study investigated the effects of BDNF polymorphism on multiple indices of memory (item, associative, prospective, subjective complaints) in a lifespan sample of 116 healthy adults aged 20-93 years. Advancing age showed a negative effect on item, associative and prospective memory, but not on subjective memory complaints. For item and prospective memory, there were significant age×BDNF group interactions, indicating the adverse effect of age on memory performance across the lifespan was much stronger in the BDNF met carriers than for the val homozygotes. BDNF met carriers also endorsed significantly greater subjective memory complaints, regardless of age, and showed a trend (p<.07) toward poorer associative memory performance compared to val homozygotes. These results suggest that genetic predisposition to the availability of brain-derived neurotrophic factor, by way of the BDNF val66met polymorphism, exerts an influence on multiple indices of episodic memory - in some cases in all individuals regardless of age (subjective memory and perhaps associative memory), in others as an exacerbation of age-related differences in memory across the lifespan (item and prospective memory). This article is part of a Special Issue entitled Memory & Aging.
脑源性神经营养因子Val66Met多态性(rs6265)影响突触中脑源性神经营养因子的活性依赖性分泌,这对学习和记忆至关重要。携带met等位基因的纯合子或杂合子个体的脑源性神经营养因子分泌低于val纯合子,可能存在陈述性记忆表现下降的风险,但尚不清楚哪些类型的陈述性记忆可能受到影响,以及脑源性神经营养因子Val66Met多态性如何影响整个生命周期的记忆老化。这项横断面研究调查了脑源性神经营养因子多态性对116名年龄在20 - 93岁的健康成年人整个生命周期样本中多种记忆指标(项目记忆、联想记忆、前瞻性记忆、主观记忆抱怨)的影响。年龄增长对项目记忆、联想记忆和前瞻性记忆有负面影响,但对主观记忆抱怨没有影响。对于项目记忆和前瞻性记忆,存在显著的年龄×脑源性神经营养因子组交互作用,表明在整个生命周期中,年龄对记忆表现的不利影响在脑源性神经营养因子met携带者中比val纯合子更强。无论年龄大小,脑源性神经营养因子met携带者也认可明显更多的主观记忆抱怨,并且与val纯合子相比,在联想记忆表现方面有较差的趋势(p<0.07)。这些结果表明,通过脑源性神经营养因子Val66Met多态性,脑源性神经营养因子可用性的遗传易感性对情景记忆的多个指标产生影响——在某些情况下对所有个体(主观记忆,可能还有联想记忆)都有影响,无论年龄大小;在其他情况下,会加剧整个生命周期中与年龄相关的记忆差异(项目记忆和前瞻性记忆)。本文是名为“记忆与衰老”的特刊的一部分。