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Impact of 5-HTTLPR on hippocampal subregional activation in older adults

机译:5-HTTLPR对老年人海马亚区域激活的影响

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摘要

Studies have shown that a functional polymorphism of the serotonin transporter gene (5-HTTLPR) impacts performance on memory-related tasks and the hippocampal structures that subserve these tasks. The short (s) allele of 5-HTTLPR has been linked to greater susceptibility for impaired memory and smaller hippocampal volume compared to the long allele (l). However, previous studies have not examined the associations between 5-HTTLPR allele and activation in subregions of the hippocampus. In this study, we used functional magnetic resonance imaging (fMRI) to measure activation in hippocampal and temporal lobe subregions in 36 elderly non-clinical participants performing a face–name encoding and recognition task. Although there were no significant differences in task performance between s allele carriers and l homozygotes, right CA1 and right parahippocampal activation during recognition errors was significantly greater in individuals bearing the s allele. In an exploratory analysis, we determined that these effects were more pronounced in s allele carriers with the apolipoprotein ɛ4 allele. Our results suggest that older individuals with the s allele inefficiently allocate neural resources while making errors in recognizing face–name associations, which could negatively impact memory performance during more challenging tasks.
机译:研究表明,血清素转运蛋白基因(5-HTTLPR)的功能多态性会影响与记忆有关的任务和为这些任务提供支持的海马结构的性能。与长等位基因(1)相比,5-HTTLPR短等位基因与记忆力减退的敏感性更高,海马体积更小有关。然而,先前的研究尚未检查5-HTTLPR等位基因与海马亚区激活之间的关联。在这项研究中,我们使用功能磁共振成像(fMRI)来测量36位执行面部名称编码和识别任务的老年非临床参与者的海马和颞叶亚区域的激活。尽管在等位基因携带者和纯合子之间的任务执行上没有显着差异,但是在带有等位基因的个体中,识别错误期间右CA1和右海马旁激活明显更大。在探索性分析中,我们确定这些作用在载脂蛋白ɛ4等位基因的s等位基因携带者中更为明显。我们的结果表明,具有等位基因的年长个体在识别面部名称关联时出错时分配神经资源的效率低下,这可能在更具挑战性的任务中对记忆性能产生负面影响。

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