Evidence map›Paper›PMID 25364774›Full record

ArticleNeurology(R) neuroimmunology & neuroinflammation2014

Antibodies to myelin oligodendrocyte glycoprotein in bilateral and recurrent optic neuritis.

Sudarshini Ramanathan, Stephen W Reddel, Andrew Henderson, John D E Parratt, Michael Barnett, Prudence N Gatt, Vera Merheb, Raani-Yogeeta Anusuiya Kumaran, Karrnan Pathmanandavel, Nese Sinmaz and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Neurology(R) neuroimmunology & neuroinflammation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03345537 (Observational Prospective Multicentered Study Evaluating Initial Clinical Presentation of Inflammatory Optic Neuritis), which is not on this map. Cited by 98 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed, 2 pooled it
12.5field-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.

NCT03345537 completednot on this mapstarted 2018, after this paper: background citation

Observational Prospective Multicentered Study Evaluating Initial Clinical Presentation of Inflammatory Optic Neuritis (ON) Associated or Not With Autoantibodies Anti- Myelin-oligodendrocyte-glycoprotein (MOG-Ab)

TypeobservationalSponsorNantes University HospitalRan2018 to 2022Enrolled103ConditionsOptic NeuritisArmsNon interventional study
3 · Its place in the literature

Who cites it

98 citing papers in PubMed, 2 syntheses or guidelines pooled it, 224 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Autoantibodies against Neurologic Antigens in Nonneurologic Autoimmunity.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Trial
  4. Trial
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. MOG antibody-associated optic neuritis.Eye (London, England) · 2024
    Review
  13. Article
  14. Review
  15. Article
  16. Double-negative neuromyelitis optica spectrum disorder.Multiple sclerosis (Houndmills, Basingstoke, England) · 2023
    Review
  17. Article
  18. Review
  19. Article
  20. Review

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

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

19 authors at 1 institution in 1 country.

Sudarshini RamanathanAuthors' affiliations are listed at the end of the article.
Stephen W ReddelAuthors' affiliations are listed at the end of the article.
Andrew HendersonAuthors' affiliations are listed at the end of the article.
John D E ParrattAuthors' affiliations are listed at the end of the article.
Michael BarnettAuthors' affiliations are listed at the end of the article.
Prudence N GattAuthors' affiliations are listed at the end of the article.
Vera MerhebAuthors' affiliations are listed at the end of the article.
Raani-Yogeeta Anusuiya KumaranAuthors' affiliations are listed at the end of the article.
Karrnan PathmanandavelAuthors' affiliations are listed at the end of the article.
Nese SinmazAuthors' affiliations are listed at the end of the article.
Mahtab GhadiriAuthors' affiliations are listed at the end of the article.
Con YiannikasAuthors' affiliations are listed at the end of the article.
Steve VucicAuthors' affiliations are listed at the end of the article.
Graeme StewartAuthors' affiliations are listed at the end of the article.
Andrew F BleaselAuthors' affiliations are listed at the end of the article.
David BoothAuthors' affiliations are listed at the end of the article.
Victor S C FungAuthors' affiliations are listed at the end of the article.
Russell C DaleAuthors' affiliations are listed at the end of the article.
Fabienne BrilotAuthors' affiliations are listed at the end of the article.
School of the Art Institute of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe examined a cohort of adults with aquaporin-4 (AQP4) antibody-negative neuromyelitis optica/neuromyelitis optica spectrum disorder (NMO/NMOSD) for antibodies to myelin oligodendrocyte glycoprotein (MOG).

methodsWe performed a flow cytometry cell-based assay using live human lentivirus-transduced cells expressing full-length surface MOG. Serum was tested in 23 AQP4 antibody-negative NMO/NMOSD patients with bilateral and/or recurrent optic neuritis (BON, n = 11), longitudinally extensive transverse myelitis (LETM, n = 10), and sequential BON and LETM (n = 2), as well as in patients with multiple sclerosis (MS, n = 76) and controls (n = 52).

resultsMOG antibodies were detected in 9/23 AQP4 antibody-negative patients with NMO/NMOSD, compared to 1/76 patients with MS and 0/52 controls (p < 0.001). MOG antibodies were detected in 8/11 patients with BON, 0/10 patients with LETM, and 1/2 patients with sequential BON and LETM. Six of 9 MOG antibody-positive patients had a relapsing course. MOG antibody-positive patients had prominent optic disc swelling and were more likely to have a rapid response to steroid therapy and relapse on steroid cessation than MOG antibody-negative patients (p = 0.034 and p = 0.029, respectively). While 8/9 MOG antibody-positive patients had good follow-up visual acuity, one experienced sustained visual impairment, 3 had retinal nerve fiber layer thinning, and one had residual spinal disability.

conclusionsMOG antibodies have a strong association with BON and may be a useful clinical biomarker. MOG antibody-associated BON is a relapsing disorder that is frequently steroid responsive and often steroid dependent. Failure to recognize the disorder early and institute immunotherapy promptly may be associated with sustained impairment. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that MOG antibodies are associated with AQP4 antibody-negative BON (sensitivity 69%, 95% confidence interval [CI] 42%-87%; specificity 99%, 95% CI 93.7%-99.8%).

Identifiers

PMID25364774
PMCPMC4215392
OpenAlexW2169522944

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.