Evidence map›Paper›PMID 42569899›Full record

ArticleEpilepsia open2026

Frequency of anti-neural antibodies and autoimmune epilepsy in focal epilepsy of unknown etiology: An observational study in a Singaporean cohort.

Seong Jin Park, Jeanne May May Tan, Xuejuan Peng, Patricia Yut Wan Wong, Karine Su Shan Tay, Angelia Swee Hoon Koe, Janis Siew Noi Tye, Josiah Yui Huei Chai, Pei Xuan Koh, Yee Leng Tan and 5 more

Abstract read
In one paragraph

Article in Epilepsia open, 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.

Seong Jin ParkDuke-NUS Medical School, Singapore, Singapore.ORCID https://orcid.org/0009-0004-3736-1448
Jeanne May May TanDuke-NUS Medical School, Singapore, Singapore.ORCID https://orcid.org/0000-0002-2049-5608
Xuejuan PengDepartment of Neurology, National Neuroscience Institute, Singapore, Singapore.
Patricia Yut Wan WongDepartment of Neurology, National Neuroscience Institute, Singapore, Singapore.
Karine Su Shan TayDepartment of Neurology, National Neuroscience Institute, Singapore, Singapore.ORCID https://orcid.org/0009-0002-3886-4923
Angelia Swee Hoon KoeDepartment of Neurology, National Neuroscience Institute, Singapore, Singapore.
Janis Siew Noi TyeDepartment of Neurology, National Neuroscience Institute, Singapore, Singapore.
Josiah Yui Huei ChaiDuke-NUS Medical School, Singapore, Singapore.
Pei Xuan KohDepartment of Neurology, National Neuroscience Institute, Singapore, Singapore.ORCID https://orcid.org/0000-0002-8795-0177
Yee Leng TanDepartment of Neurology, National Neuroscience Institute, Singapore, Singapore.ORCID https://orcid.org/0000-0003-3559-506X
Sheila SrinivasanDepartment of Neurology, National Neuroscience Institute, Singapore, Singapore.ORCID https://orcid.org/0009-0003-4035-361X
Ngai Kun LohDepartment of Neurology, National Neuroscience Institute, Singapore, Singapore.ORCID https://orcid.org/0009-0003-9309-7541
Nigel Choon Kiat TanDuke-NUS Medical School, Singapore, Singapore.ORCID https://orcid.org/0000-0002-9213-5572
Kevin TanDuke-NUS Medical School, Singapore, Singapore.ORCID https://orcid.org/0000-0001-5894-8839
Tianrong YeoDuke-NUS Medical School, Singapore, Singapore.ORCID https://orcid.org/0000-0002-3648-0953

Funding

Duke-NUS Medical School AM-ETHOS grantNational Medical Research Council Clinician Scientist Award CSAINV24jul-0004National Medical Research Council Research Training FellowshipNational Neuroscience Institute RIE2025 CG Pilot grantSingHealth Duke-NUS Clinician Investigator Advancement Award 06/2024/CIVA/04-A04
6 · The paper itself

Abstract

objectiveAutoimmune epilepsy (AES) is increasingly recognized as a condition in patients with epilepsy of unknown etiology. Early immunotherapy improves outcomes; however, data on its prevalence and the frequency of anti-neural/neuronal antibodies in Asian populations remain scarce. Herein, we aim to (1) evaluate the frequency of serum anti-neuronal/neural antibodies, (2) compare the clinical characteristics between seropositive and seronegative patients, and (3) explore the clinical utility of the ACES (Antibodies Contributing to Focal Epilepsy Signs and Symptoms) score in diagnosing AES in a cohort of Singaporean patients with focal epilepsy of unknown etiology.

methodsThis was a cross-sectional, observational, single-center study performed at the National Neuroscience Institute (NNI), Singapore. Patients with focal epilepsy of unknown etiology were prospectively recruited. Serum samples were tested using both cell-based (CBA) and immunohistochemistry (IHC)-based tissue assays. Patients were classified into definite, probable, and possible AES based on antibody positivity. Clinical characteristics, MRI and EEG findings, and ACES scores were analyzed.

resultsOne-hundred-and-twenty patients were included. Nine patients (7.50%) were seropositive on IHC, while 2 patients (1.67%) were positive on CBA (1 with concomitant IHC positivity, 1 without). In total, 10 patients (8.33%) were seropositive on IHC and/or CBA. Seropositivity was associated with female sex, autoimmune and psychiatric comorbidities, behavioral changes, speech problems, abnormal MRI brain, medial temporal T2/FLAIR hyperintensities, and ACES ≥2. AUC of ACES for seropositivity was 0.878; sensitivity and specificity were 60.0% and 96.4% respectively at a cutoff of ≥2. SIGNIFICANCE: The frequency of specific, well-characterized anti-neural/neuronal antibodies in focal epilepsy of unknown etiology is low in Singapore. Distinct clinico-radiological features, in particular those that comprise the ACES score, were useful in identifying AES. Their presence should prompt antibody testing to confirm the diagnosis of AES for earlier immunotherapy. PLAIN LANGUAGE SUMMARY: This study performed in Singapore investigated autoimmune epilepsy in people who have focal epilepsy with no clear cause. Researchers tested blood samples for antibodies linked to autoimmune epilepsy and compared clinical features between patients with and without these antibodies. Out of 120 patients, 10 had positive antibody tests-they were more often female, more likely to have autoimmune or psychiatric conditions, behavior or speech problems, and abnormal brain MRI findings. An ACES score of 2 or more was useful for identifying patients with antibodies. Using these clinical features can help clinicians decide who should be tested and treated earlier.

Indexed as

antibodiesautoimmuneepilepsyneuralneuronalsingapore

Identifiers

PMID42569899
PMCPMC13452136

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.