Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford, UK; Department of Experimental Psychology and Oxford Centre for Human Brain Activity, Wellcome Centre for Integrative Neuroimaging, Department of Psychiatry, University of Oxford, Oxford, UK.
Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Cortex. 2019 Jan;110:127-140. doi: 10.1016/j.cortex.2018.04.015. Epub 2018 May 17.
The accelerated forgetting of newly learned information is common amongst patients with epilepsy and, in particular, in the syndrome of transient epileptic amnesia (TEA). However, the neural mechanisms underlying accelerated forgetting are poorly understood. It has been hypothesised that interictal epileptiform activity during longer retention intervals disrupts normally established memory traces. Here, we tested a distinct hypothesis-that accelerated forgetting relates to the abnormal encoding of memories. We studied a group of 15 patients with TEA together with matched, healthy control subjects. Despite normal performance on standard anterograde memory tasks, patients showed accelerated forgetting of a word list over one week. We used a subsequent memory paradigm to compare encoding-related brain activity in patients and controls. Participants studied a series of visually presented scenes whilst undergoing functional MRI scanning. Recognition memory for these scenes was then probed outside the scanner after delays of 45 min and of 4 days. Patients showed poorer memory for the scenes compared with controls. In the patients but not the controls, subsequently forgotten stimuli were associated with reduced hippocampal activation at encoding. Furthermore, patients demonstrated reduced deactivation of posteromedial cortex regions upon viewing subsequently remembered stimuli as compared to subsequently forgotten ones. These data suggest that abnormal encoding-related activity in key memory areas of the brain contributes to accelerated forgetting in TEA. We propose that abnormally encoded memory traces may be particularly vulnerable to interference from subsequently encountered material and hence be forgotten more rapidly. Our results shed light on the mechanisms underlying memory impairment in epilepsy, and offer support to the proposal that accelerated forgetting may be a useful marker of subtle dysfunction in memory-related brain systems.
新学信息的加速遗忘在癫痫患者中很常见,特别是在短暂性癫痫性遗忘(TEA)综合征中。然而,加速遗忘的神经机制仍知之甚少。有人假设,较长的保留间隔期间的发作间癫痫样活动会破坏正常建立的记忆痕迹。在这里,我们测试了一个不同的假设,即加速遗忘与记忆的异常编码有关。我们研究了一组 15 名 TEA 患者以及匹配的健康对照组。尽管患者在标准顺行记忆任务中的表现正常,但他们在一周内表现出单词列表的加速遗忘。我们使用后续记忆范式来比较患者和对照组的编码相关大脑活动。参与者在功能磁共振成像扫描期间研究了一系列视觉呈现的场景。在扫描外,在 45 分钟和 4 天后对这些场景进行识别记忆测试。与对照组相比,患者对场景的记忆较差。在患者中,但不在对照组中,随后遗忘的刺激与编码时海马激活减少有关。此外,与随后遗忘的刺激相比,患者在观看随后记住的刺激时表现出后内侧皮层区域的去激活减少。这些数据表明,大脑关键记忆区域的异常编码相关活动导致 TEA 中的加速遗忘。我们提出,异常编码的记忆痕迹可能特别容易受到随后遇到的材料的干扰,因此会更快地被遗忘。我们的结果阐明了癫痫症中记忆障碍的机制,并支持加速遗忘可能是记忆相关大脑系统功能障碍的有用标志物的观点。