Evidence map›Paper›PMID 39364568›Full record

Observational studyEuropean journal of neurology2024

Immune triggers preceding neuralgic amyotrophy.

Davide Sparasci, Lenka Schilg-Hafer, Bettina Schreiner, Olivier Scheidegger, Anne-Kathrin Peyer, Agustina Maria Lascano, Alex Vicino, Bernhard Friedrich Décard, Pinelopi Tsouni, Andrea Monika Humm and 14 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in European journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Immune triggers preceding neuralgic amyotrophy.European journal of neurology · 2024
    Observational
  4. Article
  5. 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

24 authors.

Davide SparasciDepartment of Neurology, Neurocenter of Southern Switzerland EOC, Lugano, Switzerland.ORCID 0000-0002-6190-1633
Lenka Schilg-HaferDepartment of Neurology, Cantonal Hospital, St Gallen, Switzerland.
Bettina SchreinerDepartment of Neurology, University and Hospital Zurich, Zurich, Switzerland.
Olivier ScheideggerDepartment of Neurology, Inselspital, Bern University Hospital and University of Bern, Bern, Switzerland.
Anne-Kathrin PeyerDepartment of Neurology, University Hospital and University of Basel, Basel, Switzerland.
Agustina Maria LascanoNeurology Division, Department of Clinical Neuroscience, University Hospitals of Geneva and Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID 0000-0001-7572-8811
Alex VicinoNerve-Muscle Unit, Neurology Service, Department of Clinical Neurosciences, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.ORCID 0000-0001-6420-8124
Bernhard Friedrich DécardCantonal Hospital, Lucerne, Switzerland.
Pinelopi TsouniDepartment of Neurology, Hôpital du Valais, Sion, Switzerland.
Andrea Monika HummNeurology Unit, Department of Medicine, HFR Fribourg Cantonal Hospital, Fribourg, Switzerland.
Enea PianezziLaboratory of Microbiology EOC, Bellinzona, Switzerland.
Giulia ZezzaLaboratory of Microbiology EOC, Bellinzona, Switzerland.
Thomas HundsbergerDepartment of Neurology, Cantonal Hospital, St Gallen, Switzerland.
Anelia DietmannDepartment of Neurology, Inselspital, Bern University Hospital and University of Bern, Bern, Switzerland.ORCID 0000-0002-8949-0645
Hans H JungDepartment of Neurology, University and Hospital Zurich, Zurich, Switzerland.
Thierry KuntzerNerve-Muscle Unit, Neurology Service, Department of Clinical Neurosciences, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Einar Wilder-SmithDepartment of Neurology, Inselspital, Bern University Hospital and University of Bern, Bern, Switzerland.
Gladys Martinetti-LucchiniLaboratory of Microbiology EOC, Bellinzona, Switzerland.
Orlando PetriniUniversity of Applied Sciences and Arts of Southern Switzerland, Bellinzona, Switzerland.
Stefano FontanaBlood Transfusion Service SRC Southern Switzerland, Lugano, Switzerland.
Peter GowlandInterregional Blood Transfusion SRC, Bern, Switzerland.
Christoph NiederhauserInterregional Blood Transfusion SRC, Bern, Switzerland.
Claudio GobbiDepartment of Neurology, Neurocenter of Southern Switzerland EOC, Lugano, Switzerland.ORCID 0000-0002-7554-0664
Paolo RipellinoDepartment of Neurology, Neurocenter of Southern Switzerland EOC, Lugano, Switzerland.ORCID 0000-0002-8662-9656

Funding

Baasch-Medicus Stiftung, ZurichFoundation for the Advancement of Neurology, LausanneNeuromuscular Research Association Basel
6 · The paper itself

Abstract

background and purposeInfections and vaccinations have been identified as potential immunological triggers of neuralgic amyotrophy (NA), but the exact type and frequency of the preceding agents is unknown.

methodsThis was a multicentre, prospective, observational, matched case-control study. NA was diagnosed by neuromuscular experts according to validated clinical criteria and electrodiagnostic studies. Clinical data and biological samples of NA patients were collected within 90 days from disease onset between June 2018 and December 2023. All NA patients were asked about prior infection and vaccination in the month before disease onset. Serological tests for hepatitis E virus, human immunodeficiency virus, severe acute respiratory syndrome coronavirus 2, Epstein-Barr virus, cytomegalovirus, parvovirus B19, varicella-zoster virus, Borrelia burgdorferi, Mycoplasma pneumoniae and Bartonella henselae were performed in a central laboratory. Each case was matched with a healthy control for age, sex, place of residence and time of blood collection.

resultsFifty-seven patients and corresponding controls were included. The mean age was 45 years for both groups. NA onset was preceded by a symptomatic infectious trigger confirmed by microbiological tests in 15/57 (26.3%) patients. Coronavirus disease 2019 vaccination was considered a potential trigger in 7/57 (12.3%) subjects. An acute viral infection was associated with a bilateral involvement of the brachial plexus (p = 0.003, Cramèr's V = 0.43).

conclusionsConfirmed immune triggers (infection or vaccination) preceded disease onset in 22/57 (38.6%) NA cases. We suggest to test NA patients in the acute phase for intracellular antigens, especially in the case of concomitant bilateral involvement and hepatitis.

Indexed as

Brachial Plexus NeuritisAdultAgedCase-Control StudiesCOVID-19COVID-19 VaccinesFemaleHumansMaleMiddle AgedProspective StudiesCOVID-19 Vaccinesimmune triggerinfectionneuralgic amyotrophyParsonage–Turner syndromevaccination

Identifiers

PMID39364568
PMCPMC11554871

What OpenQuestion holds

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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.