Evidence map›Paper›PMID 40933287›Full record

ArticleBrain communications2025

Quantitative analysis of aquaporin-4 (AQP4) and myelin oligodendrocyte glycoprotein (MOG) antibodies titres: correlation with relapses.

Martina Nasello, Mark Woodhall, Huiru Xue, Victor Mgbachi, Ruth Geraldes, Maria Isabel Leite, Patrick Waters, Jacqueline Palace

Abstract read
In one paragraph

Article in Brain communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Use of Fluid Biomarkers in NMOSD and MOGAD: Clinical and Research Applications.Neurology(R) neuroimmunology & neuroinflammation · 2026
    Review
  2. 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

8 authors.

Martina NaselloNuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.ORCID https://orcid.org/0000-0002-1436-568X
Mark WoodhallNuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.
Huiru XueNuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.
Victor MgbachiNuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.ORCID https://orcid.org/0000-0003-0826-4687
Ruth GeraldesNuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.
Maria Isabel LeiteNuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.
Patrick WatersNuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.
Jacqueline PalaceNuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detection of antibodies against aquaporin-4 (AQP4-IgG) and myelin oligodendrocyte glycoprotein (MOG-IgG) is essential for diagnosis of AQP4-IgG+ neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein antibody-associated disease. Uncertainties persist regarding the clinical significance of serum antibody titres to predict relapses. We aimed to analyse the trend of serum AQP4-IgG and myelin oligodendrocyte glycoprotein antibody-IgG titres during relapses and periods of clinical stability. In this retrospective study we analysed serum AQP4-IgG and myelin oligodendrocyte glycoprotein antibody -IgG titres from live cell-based assays from the Oxford Autoimmune Neurology Diagnostic Laboratory for the UK specialist NMO Service between February 2010 and June 2024. We recruited seropositive AQP4-neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein antibody-associated disease patients with serum samples available within 30 days of an attack ('attack') and at least one another sample for comparison within 1 year ('pre-attack' and 'post-attack'). Up to 3 further serum samples were selected within 2, 3 or 4 years after the attack. 117 attacks in 92 AQP4-IgG+ patients (81.5% female) and 127 attacks in 111 myelin oligodendrocyte glycoprotein antibody-IgG+ patients (62.2% female) had appropriate samples. Antibody titres significantly increased from 'pre-attack' to 'attack', decreased from 'attack' to 'post-attack', and remained stable from 2 to 4 years after attacks. Long-term immunosuppressant treatments induced a further decrease in titres during remission in both cohorts. In 40% of samples in both groups there was an increase in titre at relapse. A ≥ 2-fold increase in AQP4-IgG titres had an Odds Ratio (OR) of 6.59% and 91.5% specificity of being associated with a relapse, in myelin oligodendrocyte glycoprotein antibody-IgG+ an OR of 4.87% and 88.6% specificity. 29% (26/92) AQP4-IgG+ patients became 'seronegative' during follow: most patients (64%) had low attack titres (≤100), and the time to seroreversion related the attack titre. In contrast, 41% (46/111) myelin oligodendrocyte glycoprotein antibody-IgG+ patients became 'seronegative', mostly within the first year after the attack regardless of attack titre. In conclusion, in 60% of longitudinal serum samples from patients with AQP4-IgG or myelin oligodendrocyte glycoprotein antibody-IgG there is no increase in antibody titre. When there is an increase, it is most often at relapse. A ≥ 2-fold increase in titres should be a risk particularly in case of treatment de-escalation, non-adherence to treatment or if a pseudo-relapse is suspected.

Indexed as

antibody titresimmunoglobulinsMOGADneuromyelitis optica spectrum disorder

Identifiers

PMID40933287
PMCPMC12418092

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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.