Evidence map›Paper›PMID 39054915›Full record

ArticleBrain : a journal of neurology2024

Differential reorganization of episodic and semantic memory systems in epilepsy-related mesiotemporal pathology.

Donna Gift Cabalo, Jordan DeKraker, Jessica Royer, Ke Xie, Shahin Tavakol, Raúl Rodríguez-Cruces, Andrea Bernasconi, Neda Bernasconi, Alexander Weil, Raluca Pana and 5 more

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Donna Gift CabaloMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, QC H3A 2B4, Canada.ORCID 0000-0001-9568-1723
Jordan DeKrakerMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, QC H3A 2B4, Canada.
Jessica RoyerMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, QC H3A 2B4, Canada.ORCID 0000-0002-4448-8998
Ke XieMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, QC H3A 2B4, Canada.ORCID 0000-0002-7101-2493
Shahin TavakolMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, QC H3A 2B4, Canada.
Raúl Rodríguez-CrucesMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, QC H3A 2B4, Canada.
Andrea BernasconiMontreal Neurological Institute and Hospital, McGill University, Montreal, QC H3A 2B4, Canada.ORCID 0000-0001-9358-5703
Neda BernasconiMontreal Neurological Institute and Hospital, McGill University, Montreal, QC H3A 2B4, Canada.
Alexander WeilResearch Centre, CHU St Justine, Montreal, QC H3T 1C5, Canada.
Raluca PanaMontreal Neurological Institute and Hospital, McGill University, Montreal, QC H3A 2B4, Canada.
Birgit FrauscherMontreal Neurological Institute and Hospital, McGill University, Montreal, QC H3A 2B4, Canada.ORCID 0000-0001-6064-1529
Lorenzo CaciagliDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104, USA.
Elizabeth JefferiesDepartment of Psychology, University of York, York YO10 5DD, UK.
Jonathan SmallwoodDepartment of Psychology, Queen's University, Kingston, ON K7L 3N6, Canada.
Boris C BernhardtMultimodal Imaging and Connectome Analysis Laboratory, McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, Montreal, QC H3A 2B4, Canada.ORCID 0000-0001-9256-6041

Funding

Berkeley FellowshipBrain Research UK 14181Canada First Research Excellence FundCanadian Institutes of Health Research (CIHR)Canadian Open Neuroscience PlatformChina Scholarship Council 202006070175Fonds de recherche du QuébecFRQS 1304413Gonville and Caius College, CambridgeHealthy Brains, Healthy LivesHelmholtz International BigBrain Analytics and Learning Laboratory (HIBALL)McGill UniversityNatural Sciences and Engineering Research Council of CanadaQuebec Bio-Imaging NetworkSavoy FoundationSickKids Foundation NI17-039UCL
6 · The paper itself

Abstract

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.

Indexed as

Epilepsy, Temporal LobeHippocampusMagnetic Resonance ImagingMemory, EpisodicSemanticsAdultConnectomeFemaleHumansMaleMemory DisordersMiddle AgedNeocortexNerve NetTemporal LobeYoung Adultconnectomicsdeclarative memoryepilepsygradientsmesiotemporal lobeneuroimaging

Identifiers

PMID39054915
PMCPMC11531848

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.