Evidence map›Paper›PMID 28975404›Full record

ArticleJournal of neurology2017

Neuronal autoantibodies: differentiating clinically relevant and clinically irrelevant results.

Hesham Abboud, Ian Rossman, Maureen A Mealy, Eddie Hill, Nicolas Thompson, Aditya Banerjee, John Probasco, Michael Levy

Abstract read
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In one paragraph

Article in Journal of neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Utility of the APEAnnals of clinical and translational neurology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Mimickers of autoimmune encephalitis: a literature review.The Journal of international medical research · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Presence of onconeural antibodies in sarcoidosis patients with parasarcoidosis syndrome.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2019
    Article
  17. Article
  18. Article
  19. Review
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

8 authors.

Hesham AbboudMultiple Sclerosis and Neuroimmunology Program, University Hospitals of Cleveland, Cleveland Medical Center, Bolwell, 5th Floor, 11100 Euclid Avenue, Cleveland, OH, 44106, USA. Hesham.abboud@uhhospitals.org.ORCID http://orcid.org/0000-0001-5346-8254
Ian RossmanAkron Children's Hospital, Neuro-Developmental Science Center, Akron, OH, USA.
Maureen A MealyNeurology Department, Johns Hopkins University, Baltimore, MD, USA.
Eddie HillCase Western Reserve University School of Medicine, Cleveland, OH, USA.
Nicolas ThompsonDepartment of Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, USA.
Aditya BanerjeeNeurology Department, Johns Hopkins University, Baltimore, MD, USA.
John ProbascoNeurology Department, Johns Hopkins University, Baltimore, MD, USA.
Michael LevyNeurology Department, Johns Hopkins University, Baltimore, MD, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study is to compare the rates of clinically relevant and clinically irrelevant neuronal autoantibodies among patients presenting with new neurological symptoms. We reviewed 401 neurological patients who were tested for the Mayo-Clinic paraneoplastic panel from January 2014 to December 2014 at the Johns Hopkins Hospital. We divided antibody-positive patients into two groups: clinically relevant (CR), in which a recognizable autoimmune or paraneoplastic syndrome was confirmed, and clinically irrelevant (CI), in which an autoimmune/paraneoplastic etiology was initially suspected but an alternative diagnosis was eventually found. We used Fisher's exact test for categorical variables and Mann-Whitney U test for continuous variables to identify differences between the two groups. Fifty-three patients tested positive for one or more neuronal autoantibodies. There were 17 CR (65% females, mean age 56 years), 33 CI, and 3 indeterminate patients. Compared to CI patients, CR patients were more likely to present with movement disorders or stiff person syndrome, have inflammatory CSF markers, cancer or smoking history, concomitant hyponatremia, and classical onconeuronal antibodies. CI patients were more likely to have a neuromuscular presentation, a chronic course, and antibodies against synaptic antigens. By combining the most robust differentiating factors, we developed a simple scale that predicted clinical relevance with an odds ratio of 50.3 (CI 8.2-309.9, P < 0.0001) if the score was ≥ 2. Up to 62% of neuronal autoantibody-positive patients are ultimately found to have an alternative diagnosis. Several clinical and laboratory factors can differentiate CR from CI patients to aid in interpretation of positive results.

Indexed as

Demyelinating DiseasesGastrointestinal DiseasesNeuromuscular DiseasesParaneoplastic Syndromes, Nervous SystemAdultAgedAutoantibodiesFemaleHumansMaleMiddle AgedNerve Tissue ProteinsRetrospective StudiesAutoantibodiesNerve Tissue ProteinsAntibodiesAutoimmune encephalitisClinical relevanceParaneoplastic

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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.