癫痫相关颞中叶病变中情节记忆和语义记忆系统的差异重组

IF 10.6 1区 医学 Q1 CLINICAL NEUROLOGY
Brain Pub Date : 2024-11-04 DOI:10.1093/brain/awae197
Donna Gift Cabalo, Jordan DeKraker, Jessica Royer, Ke Xie, Shahin Tavakol, Raúl Rodríguez-Cruces, Andrea Bernasconi, Neda Bernasconi, Alexander Weil, Raluca Pana, Birgit Frauscher, Lorenzo Caciagli, Elizabeth Jefferies, Jonathan Smallwood, Boris C Bernhardt
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引用次数: 0

摘要

陈述性记忆包括外显记忆和语义记忆。外显记忆捕捉具有特定时空关系的单个事件,而语义记忆则储存与上下文无关的知识。行为和功能神经影像学研究揭示了这两种记忆系统的共同和不同的神经基底,牵涉到中颞叶(MTL)区域,如海马和分布式新皮质。在此,我们以单侧颞叶癫痫(TLE)患者为人类疾病模型,探讨了陈述性记忆系统的重组,以检验不同程度的MTL病变对记忆功能的影响。我们的研究队列包括31名TLE患者和60名年龄和性别匹配的健康对照者,所有参与者都在多模态核磁共振成像过程中接受了情节和语义检索任务。功能性磁共振成像任务在刺激和试验设计方面密切匹配。利用非线性连通组梯度图技术,我们得出了基于任务的外显记忆和语义记忆状态下MTL和新皮层网络的功能拓扑图。通过比较TLE患者和健康对照组的新皮层和海马功能梯度,我们观察到在表观记忆状态下,新皮层和MTL系统都发生了明显的拓扑重组。新皮质改变的特点是,TLE患者两个半球的侧颞皮质和中线顶叶皮质的功能分化减少。另一方面,在MTL中,患者在发作灶和病理核心同侧的海马后段和前段的功能分化更为明显,这表明海马内连接受到了干扰。在双侧外侧颞区和同侧角区也发现了语义记忆重组,而海马功能拓扑图未受影响。利用MTL病理学的核磁共振成像代用指标,我们进一步观察到海马微观结构和形态的改变与TLE相关的外显记忆功能重组有关。此外,相关性分析和统计中介模型显示,这些功能改变导致了患者在情节记忆中的行为缺陷,但并不包括语义记忆。总之,我们的研究结果表明,语义记忆过程依赖于分布式的新皮层网络,而情节记忆过程则由涉及海马和新皮层的网络支持。这些网络的改变可以为与中髓损伤(如TLE)相关的状态依赖性重组提供一个紧凑的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential reorganization of episodic and semantic memory systems in epilepsy-related mesiotemporal pathology.

Declarative memory encompasses episodic and semantic divisions. Episodic memory captures singular events with specific spatiotemporal relationships, whereas semantic memory houses context-independent knowledge. Behavioural and functional neuroimaging studies have revealed common and distinct neural substrates of both memory systems, implicating mesiotemporal lobe (MTL) regions such as the hippocampus and distributed neocortices. Here, we explored declarative memory system reorganization in patients with unilateral temporal lobe epilepsy (TLE) as a human disease model to test the impact of variable degrees of MTL pathology on memory function. Our cohort included 31 patients with TLE and 60 age- and sex-matched healthy controls, and all participants underwent episodic and semantic retrieval tasks during a multimodal MRI session. The functional MRI tasks were closely matched in terms of stimuli and trial design. Capitalizing on non-linear connectome gradient-mapping techniques, we derived task-based functional topographies during episodic and semantic memory states, in both the MTL and neocortical networks. Comparing neocortical and hippocampal functional gradients between TLE patients and healthy controls, we observed a marked topographic reorganization of both neocortical and MTL systems during episodic memory states. Neocortical alterations were characterized by reduced functional differentiation in TLE across lateral temporal and midline parietal cortices in both hemispheres. In the MTL, in contrast, patients presented with a more marked functional differentiation of posterior and anterior hippocampal segments ipsilateral to the seizure focus and pathological core, indicating perturbed intrahippocampal connectivity. Semantic memory reorganization was also found in bilateral lateral temporal and ipsilateral angular regions, whereas hippocampal functional topographies were unaffected. Furthermore, leveraging MRI proxies of MTL pathology, we observed alterations in hippocampal microstructure and morphology that were associated with TLE-related functional reorganization during episodic memory. Moreover, correlation analysis and statistical mediation models revealed that these functional alterations contributed to behavioural deficits in episodic memory, but again not in semantic memory in patients. Altogether, our findings suggest that semantic processes rely on distributed neocortical networks, whereas episodic processes are supported by a network involving both the hippocampus and the neocortex. Alterations of such networks can provide a compact signature of state-dependent reorganization in conditions associated with MTL damage, such as TLE.

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来源期刊
Brain
Brain 医学-临床神经学
CiteScore
20.30
自引率
4.10%
发文量
458
审稿时长
3-6 weeks
期刊介绍: Brain, a journal focused on clinical neurology and translational neuroscience, has been publishing landmark papers since 1878. The journal aims to expand its scope by including studies that shed light on disease mechanisms and conducting innovative clinical trials for brain disorders. With a wide range of topics covered, the Editorial Board represents the international readership and diverse coverage of the journal. Accepted articles are promptly posted online, typically within a few weeks of acceptance. As of 2022, Brain holds an impressive impact factor of 14.5, according to the Journal Citation Reports.
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