Evidence map›Paper›PMID 29667271›Full record

ArticleEuropean journal of neurology2018

Syndrome and outcome of antibody-negative limbic encephalitis.

F Graus, D Escudero, L Oleaga, J Bruna, A Villarejo-Galende, J Ballabriga, M I Barceló, F Gilo, S Popkirov, P Stourac and 1 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in European journal of neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
10.0field-weighted citation impact, top 1% 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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 144 citations in OpenAlex.

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8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 9 institutions in 4 countries.

F GrausNeuroimmunology Program, Institut d'Investigació Biomèdica August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
D EscuderoService of Neurology, Hospital Clinic, Barcelona, Spain.ORCID 0000-0002-6852-6936
L OleagaDepartment of Radiology, Hospital Clinic, Barcelona, Spain.
J BrunaUnit of Neuro-Oncology, Hospital de Bellvitge, Institut Català d'Oncologia (ICO) L'Hospitalet, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Hospitalet del Llobregat, Spain.ORCID 0000-0001-6895-5047
A Villarejo-GalendeService of Neurology, Hospital 12 de Octubre, Madrid, Spain.
J BallabrigaService of Neurology, Hospital Son Llatzer, Palma de Mallorca, Spain.
M I BarcelóService of Neurology, Hospital Son Espases, Palma de Mallorca, Spain.
F GiloService of Neurology, Hospital Nuestra Señora del Rosario, Madrid, Spain.
S PopkirovDepartment of Neurology, University Hospital Knappschaftskrankenhaus Bochum, Ruhr-University Bochum, Bochum, Germany.
P StouracDepartment of Neurology, Masaryk University and University Hospital, Brno, Czech Republic.
J DalmauNeuroimmunology Program, Institut d'Investigació Biomèdica August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
Hospital Clínic de Barcelona · ESHospital Nuestra Señora de Alarcos · ESHospital Son Llatzer · ESHospital Universitario Son Espases · ESInstitució Catalana de Recerca i Estudis Avançats · ESInstitut d'Investigació Biomédica de Bellvitge · ESMasaryk University · CZResearch Institute Hospital 12 de Octubre · ESUniversitätsklinikum Knappschaftskrankenhaus Bochum · DE

Funding

Paraneoplastic Disorders of the CNS: Autoantigen ProfilingR01NS077851 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI DALMAU, JOSEP O. · 2011 to 2015
$1.9M
NINDS NIH HHS R01 NS077851
6 · The paper itself

Abstract

background and purposeThe aim was to report the clinical characteristics of 12 patients with limbic encephalitis (LE) who were antibody-negative after a comprehensive immunological study.

methodsThe clinical records of 163 patients with LE were reviewed. Immunohistochemistry on rat brain, cultured neurons and cell-based assays were used to identify neuronal autoantibodies. Patients were included if (i) there was adequate clinical, cerebrospinal fluid (CSF) and magnetic resonance imaging information to classify the syndrome as LE, (ii) magnetic resonance images were accessible for central review and (iii) serum and CSF were available and were confirmed negative for neuronal antibodies.

resultsTwelve (7%) of 163 LE patients [median age 62 years; range 40-79; 9 (75%) male] without neuronal autoantibodies were identified. The most frequent initial complaints were deficits in short-term memory leading to hospital admission in a few weeks (median time 2 weeks; range 0.5-12). In four patients the short-term memory dysfunction remained as an isolated symptom during the entire course of the disease. Seizures, drowsiness and psychiatric problems were unusual. Four patients had solid tumors (one lung, one esophagus, two metastatic cervical adenopathies of unknown primary tumor) and one chronic lymphocytic leukemia. CSF showed pleocytosis in seven (58%) with a median of 13 white blood cells/mm

conclusionsDespite the discovery of new antibodies, 7% of LE patients remain seronegative. Antibody-negative LE is more frequent in older males and usually develops with predominant or isolated short-term memory loss. Despite the absence of antibodies, patients may have an underlying cancer and respond to immunotherapy.

Indexed as

AdultAgedAnimalsAutoantibodiesAutoantigensCells, CulturedFemaleHumansImmunohistochemistryImmunotherapyLeukocytesLeukocytosisLimbic EncephalitisMagnetic Resonance ImagingMaleMemory DisordersAutoantibodiesAutoantigensantibodiesautoimmunelimbic encephalitisparaneoplastic

Identifiers

PMID29667271
PMCPMC6037545
OpenAlexW2800863330

What OpenQuestion holds

Textmetadata
LicenceTDM
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.