Evidence map›Paper›PMID 41568938›Full record

ArticleJournal of neuroimaging : official journal of the American Society of Neuroimaging

T1w/T2w Ratio Identifies the Basolateral Amygdala as a Preferential Target in Autoimmune Limbic Encephalitis.

Rakshit Dadarwal, Andre Dik, Laura Bierhansl, Noëmi Gmahl, Nils C Landmeyer, Tobias J Brix, Veronika K Jaeger, Jochen Bauer, Wilhelm Küker, Heinz Wiendl and 3 more

Abstract read
In one paragraph

Article in Journal of neuroimaging : official journal of the American Society of Neuroimaging. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. T1w/T2w Ratio Identifies the Basolateral Amygdala as a Preferential Target in Autoimmune Limbic Encephalitis.Journal of neuroimaging : official journal of the American Society of Neuroimaging
    Article
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

13 authors.

Rakshit DadarwalDepartment of Neurology, University Hospital Muenster, Muenster, Germany.ORCID https://orcid.org/0000-0003-3091-2580
Andre DikDepartment of Neurology, University Hospital Muenster, Muenster, Germany.
Laura BierhanslDepartment of Neurology, University Hospital Muenster, Muenster, Germany.ORCID https://orcid.org/0000-0002-6752-690X
Noëmi GmahlDepartment of Neurology, University Hospital Muenster, Muenster, Germany.
Nils C LandmeyerDepartment of Neurology, University Hospital Muenster, Muenster, Germany.
Tobias J BrixInstitute of Medical Informatics, University of Muenster, Muenster, Germany.
Veronika K JaegerInstitute of Epidemiology and Social Medicine, University of Muenster, Muenster, Germany.
Jochen BauerDepartment of Clinical Radiology, University Hospital Muenster, Muenster, Germany.
Wilhelm KükerDepartment of Clinical Radiology, University Hospital Muenster, Muenster, Germany.
Heinz WiendlDepartment of Neurology, University Hospital Muenster, Muenster, Germany.
Christian E ElgerDepartment of Neurology, University Hospital Muenster, Muenster, Germany.
Stjepana KovacDepartment of Neurology, University Hospital Muenster, Muenster, Germany.
Antje BischofDepartment of Neurology, University Hospital Muenster, Muenster, Germany.

Funding

Bundesministerium für Forschung, Technologie und RaumfahrtDeanery of the University of MuensterDeutsche ForschungsgesellschaftInnovative Medizinische Forschung
6 · The paper itself

Abstract

background and purposeThe amygdala plays a key role in the pathophysiology of autoimmune limbic encephalitis (ALE), contributing to epileptic seizures and neuropsychiatric symptoms. While no study has examined microstructural changes in individual amygdala nuclei in ALE, we used the T1-weighted/T2-weighted (T1w/T2w) ratio to explore amygdalar pathology and its associations with clinical manifestations, including epilepsy and neuropsychiatric symptoms.

methodsThis single-center study examined 57 patients diagnosed with ALE and 16 healthy controls (HC). Patients underwent a comprehensive assessment that included clinical, electroencephalogram (EEG), magnetic resonance imaging (MRI), and neuropsychological assessments. Patients were stratified by epileptic focus based on long-term EEG. T1w/T2w ratio and volumetric measures of the amygdala and its nuclei were analyzed and correlated with epileptic focus and neuropsychiatric outcomes.

resultsEEG revealed 26 left temporal, 26 bitemporal, and five right temporal epileptic foci. The T1w/T2w ratio in the left amygdala was markedly reduced in patients with left temporal (p = 0.013) and bitemporal (p = 0.018) epileptic foci compared to HC. This reduction was most pronounced in the left basolateral complex (p = 0.011). Whereas amygdalar volumes were similar between patients and HC, exploratory analyses showed an increased volume of the left lateral nucleus in left temporal ALE (p = 0.036). Furthermore, we found no correlations between MRI measures and neuropsychiatric scores.

conclusionOur findings indicate that the basolateral complex of the amygdala is preferentially affected in ALE, suggesting a region-specific vulnerability to autoimmune-mediated inflammation. T1w/T2w ratio alterations reflect the epileptogenic focus and may serve as a clinically accessible, noninvasive biomarker for early diagnosis and treatment monitoring in ALE.

Indexed as

Autoimmune DiseasesBasolateral Nuclear ComplexLimbic EncephalitisMagnetic Resonance ImagingAdultAmygdalaElectroencephalographyFemaleHumansMaleMiddle AgedYoung Adultamygdala nucleiautoimmune limbic encephalitisepilepsyMRIT1w/T2w ratio

Identifiers

PMID41568938
PMCPMC12825940

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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.