Evidence map›Paper›PMID 36247087›Full record

ArticleJournal of translational autoimmunity2022

Increased T- and B-cells associated with the phenotype of autoimmune limbic encephalitis with mainly memory dysfunction.

Niels Hansen, Guido Widman, Demet Önder, Kerstin Schwing, Pitshaporn Leelaarporn, Indra Prusseit, Randi von Wrede, Rainer Surges, Albert J Becker, Juri-Alexander Witt and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational autoimmunity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 34% of its field
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

12 authors at 2 institutions in 1 country.

Niels HansenDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
Guido WidmanDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
Demet ÖnderDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
Kerstin SchwingDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
Pitshaporn LeelaarpornDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
Indra PrusseitDepartment of Neuropathology, University of Bonn Medical Center, Venusberg - Campus 1, 53127, Bonn, Germany.
Randi von WredeDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
Rainer SurgesDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
Albert J BeckerDepartment of Neuropathology, University of Bonn Medical Center, Venusberg - Campus 1, 53127, Bonn, Germany.
Juri-Alexander WittDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
Christian E ElgerDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
Christoph HelmstaedterDepartment of Epileptology, University Hospital Bonn, Venusberg - Campus 1, 53127, Bonn, Germany.
University Hospital Bonn · DEUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Our goal is to investigate the autoantibodies' presence and immune cells in the bioprobes of autoimmune encephalitis (AE) patients with distinct phenotypes as a promising target in AE. Methods: We retrospectively analyzed immune cells via flow cytometry, serum and cerebrospinal fluid (CSF) autoantibodies, electroencephalography, magnetic resonance imaging in 94 AE patients with suspected temporal lobe epilepsy and classified neuropsychological phenotypes according to their occurrence. Results: We detected different phenotypes in 94 AE patients [10.6% with isolated memory dysfunction (MEM), 11.7% with mood-dysfunction, 12.7% with mood and memory dysfunction, 13.8% with memory and attention dysfunction, 18.1% with memory, mood and attention disturbances and 20.2% with no mood, memory or attention dysfunction]. We did discern a relevant association of phenotypes and CSF antibody-positivity on CSF CD4 Discussion: Taken together, the phenotypes in combination with CSF antibody-positivity are biomarkers for stratifying patients. Furthermore, our results confirm the role of CD4

Indexed as

AutoantibodiesAutoimmune encephalitisImmune cellsNeuropsychologyPhenotypeVerbal memory

Identifiers

PMID36247087
PMCPMC9563330
OpenAlexW4297433704

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.