Evidence map›Paper›PMID 31624178›Full record

ArticleNeurology(R) neuroimmunology & neuroinflammation2019

Normal gut microbiome in NMDA receptor encephalitis.

Julia Herken, Corinna Bang, Malte C Rühlemann, Carsten Finke, Johanna Klag, Andre Franke, Harald Prüss

Open access · goldAbstract read
In one paragraph

Article in Neurology(R) neuroimmunology & neuroinflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Article
  8. Review
  9. Autoantibodies in neurological disease.Nature reviews. Immunology · 2021
    Review
  10. Observational
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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

7 authors at 1 institution in 1 country.

Julia HerkenFrom the German Center for Neurodegenerative Diseases (DZNE) (J.H., H.P.); Department of Neurology and Experimental Neurology (J.H., C.F., J.K., H.P.), Charité - Universitätsmedizin, Berlin; and Institute of Clinical Molecular Biology (C.B., M.C.R., A.F.), Christian Albrechts University of Kiel, Germany.
Corinna BangFrom the German Center for Neurodegenerative Diseases (DZNE) (J.H., H.P.); Department of Neurology and Experimental Neurology (J.H., C.F., J.K., H.P.), Charité - Universitätsmedizin, Berlin; and Institute of Clinical Molecular Biology (C.B., M.C.R., A.F.), Christian Albrechts University of Kiel, Germany.
Malte C RühlemannFrom the German Center for Neurodegenerative Diseases (DZNE) (J.H., H.P.); Department of Neurology and Experimental Neurology (J.H., C.F., J.K., H.P.), Charité - Universitätsmedizin, Berlin; and Institute of Clinical Molecular Biology (C.B., M.C.R., A.F.), Christian Albrechts University of Kiel, Germany.
Carsten FinkeFrom the German Center for Neurodegenerative Diseases (DZNE) (J.H., H.P.); Department of Neurology and Experimental Neurology (J.H., C.F., J.K., H.P.), Charité - Universitätsmedizin, Berlin; and Institute of Clinical Molecular Biology (C.B., M.C.R., A.F.), Christian Albrechts University of Kiel, Germany.
Johanna KlagFrom the German Center for Neurodegenerative Diseases (DZNE) (J.H., H.P.); Department of Neurology and Experimental Neurology (J.H., C.F., J.K., H.P.), Charité - Universitätsmedizin, Berlin; and Institute of Clinical Molecular Biology (C.B., M.C.R., A.F.), Christian Albrechts University of Kiel, Germany.
Andre FrankeFrom the German Center for Neurodegenerative Diseases (DZNE) (J.H., H.P.); Department of Neurology and Experimental Neurology (J.H., C.F., J.K., H.P.), Charité - Universitätsmedizin, Berlin; and Institute of Clinical Molecular Biology (C.B., M.C.R., A.F.), Christian Albrechts University of Kiel, Germany.
Harald PrüssFrom the German Center for Neurodegenerative Diseases (DZNE) (J.H., H.P.); Department of Neurology and Experimental Neurology (J.H., C.F., J.K., H.P.), Charité - Universitätsmedizin, Berlin; and Institute of Clinical Molecular Biology (C.B., M.C.R., A.F.), Christian Albrechts University of Kiel, Germany. harald.pruess@charite.de.
German Center for Neurodegenerative Diseases · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine whether the gut microbiota shows overabundance of commensal bacteria species in patients with anti-NMDA receptor (NMDAR) encephalitis, similar to patients with MS or neuromyelitis optica where they potentially balance pro- and anti-inflammatory immune responses or participate in disease pathogenesis by molecular mimicry.

methodsIntestinal microbiota was characterized in patients with NMDAR encephalitis (n = 23, mean age: 34 ± 12.7 years; 21 females) and age/sex/environment-matched healthy controls (n = 24, 40 ± 14.2 years; 22 females) using stool bacteria 16S rDNA sequencing and classification in operational taxonomic units (OTUs). Statistical analyses focused on intraindividual and interindividual bacterial diversity and identification of differentially abundant taxa.

resultsPatients with NMDAR encephalitis and controls had similar microbiome profiles of the gut microbiota regarding intraindividual bacterial diversity, OTU distribution, ratio between regional and local species diversity when testing all OTUs, and genera with a relative abundance greater than 0.5%. Similarly, the subgroup of NMDAR encephalitis patients with an ovarian teratoma (n = 3) showed no differences in microbiome variation compared with controls. Patients in the acute encephalitis stage (n = 8) showed significant differences in the numbers of

conclusionPatients with NMDAR encephalitis and controls both had a normal gut microbiome. The lack of overabundance of certain bacterial species in patients suggests that microbiome changes are no major contributors to the pathogenesis, disease course, or prognosis in NMDAR encephalitis. Despite the small sample size and heterogeneous groups, findings indicate differences to other neuroimmunologic diseases.

Indexed as

Gastrointestinal MicrobiomeAcute DiseaseAdultAnti-N-Methyl-D-Aspartate Receptor EncephalitisFecesFemaleHumansMaleMiddle Aged

Identifiers

PMID31624178
PMCPMC6857909
OpenAlexW2980478481

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.