Evidence map›Paper›PMID 41806514›Full record

ArticleEpilepsy research2026

Face-name associative memory in temporal lobe epilepsy: Region-specific insights in right-hemisphere onset.

Alena Stasenko, Adam J Schadler, Erik Kaestner, Christine N Smith, Evan Brady, Michelle S Kim, Daniel J Peterson, Claire Urbanic, Jerry J Shih, Taha Gholipour and 5 more

Abstract read
In one paragraph

Article in Epilepsy research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Alena StasenkoDepartment of Radiation Medicine & Applied Sciences, University of California San Diego, USA. Electronic address: astasenko@ucsd.edu.
Adam J SchadlerDepartment of Radiation Medicine & Applied Sciences, University of California San Diego, USA.
Erik KaestnerDepartment of Radiation Medicine & Applied Sciences, University of California San Diego, USA.
Christine N SmithDepartment of Psychiatry, University of California San Diego, USA; Veterans Affairs San Diego Healthcare System, San Diego, USA; Center for the Neurobiology of Learning and Memory, University of California Irvine, USA.
Evan BradyDepartment of Neurology, Emory University, USA.
Michelle S KimDepartment of Neurology, University of Washington, USA.
Daniel J PetersonDepartment of Radiology, University of Washington, USA.
Claire UrbanicUniversity of California Davis, USA.
Jerry J ShihDepartment of Neurosciences, University of California San Diego, USA.
Taha GholipourDepartment of Neurosciences, University of California San Diego, USA.
G Andrew JamesDepartment of Psychiatry, University of Arkansas for Medical Sciences, USA.
Deqiang QiuDepartment of Radiology, Emory University, USA.
Benjamin M HampsteadResearch Program on Cognition and Neuromodulation Based Interventions, Departments of Psychiatry and Neurology, University of Michigan, Ann Arbor, USA; Mental Health Service, VA Ann Arbor Healthcare System, Ann Arbor, MI, USA.
Daniel L DraneDepartment of Neurology, Emory University, USA; Department of Neurology, University of Washington, USA; Department of Pediatrics, Emory University, USA.
Carrie R McDonaldDepartment of Radiation Medicine & Applied Sciences, University of California San Diego, USA; Department of Psychiatry, University of California San Diego, USA.

Funding

Dissecting the Cognitive Roles of Hippocampus, Other Temporal Lobe StructuresR01NS088748 · NINDS · EMORY UNIVERSITY · PI DRANE, DANIEL L · 2014 to 2024
$6.4M
Multimodal Imaging of Language in the Preoperative Evaluation of EpilepsyR01NS065838 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MCDONALD, CARRIE R · 2010 to 2018
$4.4M
Research Program on Cognition and Neuromodulation Based Interventions (RP-CNBI)R35AG072262 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HAMPSTEAD, BENJAMIN MICHAEL · 2021 to 2025
$4.2M
Multimodal imaging of memory in epilepsy from whole brain networks to local neuronal responses: Implications for surgical decision-makingR01NS124585 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MCDONALD, CARRIE R · 2022 to 2025
$3.3M
Whole Head Magnetoencephalography (MEG) SystemS10OD034302 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LEE, ROLAND ROBERT · 2023 to 2023
$2.0M
Predicting epilepsy surgery outcomes from individualized resting state functional anomaliesK23NS135108 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Taha Gholipour · 2024 to 2026
$703k
Chronic Monitoring for a Chronic Condition: Leveraging Digital Assessment to Determine Lifestyle Impacts on Cognitive Aging in EpilepsyK23NS142707 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Alena Stasenko · 2025 to 2026
$444k
Development of a personalized neurostimulation protocol for memory mapping in epilepsyK01NS124831 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KAESTNER, ERIK JORDAN · 2022 to 2024
$339k
NIA NIH HHS R35 AG072262NIH HHS S10 OD034302NINDS NIH HHS K01 NS124831NINDS NIH HHS K23 NS135108NINDS NIH HHS K23 NS142707NINDS NIH HHS R01 NS065838NINDS NIH HHS R01 NS088748NINDS NIH HHS R01 NS124585
6 · The paper itself

Abstract

Mapping memory function in temporal lobe epilepsy (TLE) is important for understanding surgical risk, yet practical noninvasive tools remain limited. We tested whether a face-name associative memory fMRI task could detect subregional dysfunction within the amygdala-hippocampal complex (AHC) in TLE. Forty-nine individuals with unilateral TLE (29 left-, 20 right-onset; 51% MTS-negative) and 25 controls from three centers were scanned during a face-name encoding task and completed delayed recognition and neuropsychological tests of memory. The hippocampal head, body, tail, and amygdala were anatomically segmented, and activation was examined for encoding and novelty contrasts. In controls, AHC activation was predominantly right-lateralized. For encoding, a Region × Hemisphere × Group interaction showed reduced ipsilateral amygdala and hippocampal tail activation in right TLE, with relative preservation in other subregions. Left TLE showed a nonsignificant medium effect in the ipsilateral amygdala. In right TLE, greater contralateral amygdala activation correlated with better face-name recognition and verbal memory, while greater ipsilateral hippocampal tail activation correlated with better verbal and visual memory. Findings were independent of mesial temporal sclerosis and hippocampal volume. A brief, ecologically valid face-name fMRI task revealed lateralized, subregion-specific disruption in right TLE and behaviorally relevant variability in the amygdala and posterior hippocampal engagement. Future work is needed to determine whether these activation patterns predict post-surgical memory outcomes.

Indexed as

Association LearningEpilepsy, Temporal LobeFacial RecognitionFunctional LateralityMemoryAdultAmygdalaBrain MappingFaceFemaleHippocampal SclerosisHippocampusHumansMagnetic Resonance ImagingMaleMiddle AgedFMRIFunctional, Magnetic resonance imagingFunctional reserveLearning and memoryMemoryTemporal lobe epilepsyTLE

Identifiers

PMID41806514
PMCPMC13480061

What OpenQuestion holds

Textmetadata
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.