Evidence map›Paper›PMID 42615230›Full record

ArticleEpilepsia2026

Nucleus basalis functional connectivity aberrations in temporal lobe epilepsy and improvements after successful epilepsy surgery.

Addison C Cavender, Derek J Doss, Ghassan S Makhoul, Bruno Hidalgo Monroy Lerma, Anas Reda, C Price Withers, Emily Liao, Kate Wang, Hernán F J González, Sarah E Goodale and 6 more

Abstract read
In one paragraph

Article in Epilepsia, 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

16 authors.

Addison C CavenderVanderbilt Brain Institute, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0009-0007-0153-8979
Derek J DossVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-2685-0762
Ghassan S MakhoulVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.
Bruno Hidalgo Monroy LermaVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0009-0000-7307-4762
Anas RedaVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0009-0009-9782-2505
C Price WithersVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.
Emily LiaoDepartment of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Kate WangDepartment of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0009-0000-2913-5708
Hernán F J GonzálezDepartment of Neurological Surgery, University of California, San Diego, La Jolla, California, USA.
Sarah E GoodaleVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.
Graham W JohnsonDepartment of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Laurie E CuttingVanderbilt Brain Institute, Vanderbilt University, Nashville, Tennessee, USA.
Sarah K BickVanderbilt Institute for Surgery and Engineering, Vanderbilt University, Nashville, Tennessee, USA.
Catie ChangVanderbilt Brain Institute, Vanderbilt University, Nashville, Tennessee, USA.
Victoria L MorganVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0001-8263-2324
Dario J EnglotVanderbilt Brain Institute, Vanderbilt University, Nashville, Tennessee, USA.

Funding

Relating Vigilance to Connectivity and Neurocognition in Temporal Lobe EpilepsyR01NS112252 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ENGLOT, DARIO J · 2019 to 2023
$3.0M
MRI Connectivity Biomarkers of Treatment Response in Focal EpilepsyR01NS108445 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MORGAN, VICTORIA L · 2019 to 2024
$2.5M
Development of multimodal network analyses to improve epilepsy surgery outcomesR01NS134625 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Dario J Englot · 2024 to 2026
$2.0M
Arousal Network Dysfunction in Temporal Lobe Epilepsy: Origins, Contributions, and ReversibilityR01NS146021 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Dario J Englot · 2026 to 2026
$689k
Dynamic multimodal connectivity analysis of brain networks in focal epilepsyF31NS131056 · NINDS · VANDERBILT UNIVERSITY · PI DOSS, DEREK J · 2023 to 2024
$60k
Neil and Barbara SmitNIH HHS F31NS131056NIH HHS R01NS108445NIH HHS R01NS112252NIH HHS R01NS134625NINDS NIH HHS R01 NS112252NINDS NIH HHS R01 NS134625NINDS NIH HHS R01 NS146021
6 · The paper itself

Abstract

objectiveResective surgery achieves seizure freedom in approximately 60%-80% of patients with drug-resistant temporal lobe epilepsy (TLE), yet the extent to which seizure cessation permits recovery of disrupted functional brain networks remains unclear. Increasing evidence suggests that recurrent seizures alter subcortical-cortical communication involved in arousal and cognition, contributing to chronic interictal deficits, such as in executive function. Prior work demonstrates that the nucleus basalis of Meynert (NBM), the primary source of cortical cholinergic input to the cortex, exhibits aberrant functional connectivity in patients with TLE. We examined NBM connectivity in patients with TLE before and after surgery using patient-specific NBM segmentations. We sought to investigate whether seizure freedom is associated with recovery of NBM functional connectivity, consistent with previous observations of interictal network dysfunction reversal in other subcortical arousal structures.

methodsResting-state functional magnetic resonance imaging was analyzed in 75 patients with TLE, including 34 patients postoperatively, and 106 controls. Patient-specific NBM segmentations were used to compute functional connectivity between the NBM and frontoparietal association cortex (FPAC) and across the whole brain. Subcortical arousal network community structure was assessed using community detection. Postoperative network changes were evaluated relative to seizure outcome.

resultsPrior to surgery, patients exhibited reduced bilateral NBM connectivity to the FPAC and whole brain compared to controls, indicating widespread cholinergic network disruption beyond the ipsilateral hemisphere. Following surgery, NBM connectivity increased and no longer differed from controls. Seizure-free patients demonstrated greater postoperative increases in ipsilateral NBM-FPAC connectivity than non-seizure-free patients, which was not explained by time to postoperative scan or volumetric change. Subcortical arousal community structure remained altered postoperatively. SIGNIFICANCE: Successful TLE surgery is associated with partial restoration of cholinergic arousal network connectivity, supporting the idea that seizure cessation enables recovery of brain networks disrupted by recurrent seizures. These findings position the NBM as a potential biomarker of network recovery following epilepsy surgery.

Indexed as

brain networksfunctional neuroimagingMRIseizures

Identifiers

PMID42615230
PMCPMC13650722

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.