Evidence map›Paper›PMID 34362853›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2022

Silent progression of brain atrophy in aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder.

Hiroki Masuda, Masahiro Mori, Shigeki Hirano, Akiyuki Uzawa, Tomohiko Uchida, Mayumi Muto, Ryohei Ohtani, Reiji Aoki, Satoshi Kuwabara

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07526298 (Anticipating Irreversible Disability in Neuromyelitis Optica Spectrum Disorder), which is not on this map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
3.9field-weighted citation impact, top 6% 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.

NCT07526298 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Anticipating Irreversible Disability in Neuromyelitis Optica Spectrum Disorder: a Multicenter Prospective Observational Study to Assess Disease Activity in Apparently Stable Patients

Typeobservational_patient_registrySponsorIRCCS San RaffaeleRan2026 to 2027Enrolled50ConditionsNeuromyelitis Optica Spectrum DisordersArmsMRI, Immunological Factors
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.

  1. Pooled it
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  11. Article
  12. Emerging Role of Targeted Monoclonal Antibodies in Neuromyelitis Optica Spectrum Disorders.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  13. Association of peripapillary retinal nerve fiber layer atrophy with cognitive impairment in patients with neuromyelitis optica spectrum disorder.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  14. Article
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  20. CD11cNeurology(R) neuroimmunology & neuroinflammation · 2024
    Observational
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

9 authors at 1 institution in 1 country.

Hiroki MasudaNeurology, Chiba University Graduate School of Medicine School of Medicine, Chiba, Japan.ORCID 0000-0002-4106-6482
Masahiro MoriNeurology, Chiba University Graduate School of Medicine School of Medicine, Chiba, Japan morim@faculty.chiba-u.jp.ORCID 0000-0002-8767-255X
Shigeki HiranoNeurology, Chiba University Graduate School of Medicine School of Medicine, Chiba, Japan.ORCID 0000-0003-3473-2317
Akiyuki UzawaNeurology, Chiba University Graduate School of Medicine School of Medicine, Chiba, Japan.ORCID 0000-0001-9252-1863
Tomohiko UchidaNeurology, Chiba University Graduate School of Medicine School of Medicine, Chiba, Japan.
Mayumi MutoNeurology, Chiba University Graduate School of Medicine School of Medicine, Chiba, Japan.
Ryohei OhtaniNeurology, Chiba University Graduate School of Medicine School of Medicine, Chiba, Japan.
Reiji AokiNeurology, Chiba University Graduate School of Medicine School of Medicine, Chiba, Japan.
Satoshi KuwabaraNeurology, Chiba University Graduate School of Medicine School of Medicine, Chiba, Japan.ORCID 0000-0002-4716-8578
Chiba University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate longitudinal brain atrophy in patients with neuromyelitis optica spectrum disorder (NMOSD).

methodsWe investigated the longitudinal brain atrophy rate in patients with aquaporin-4 antibody-positive NMOSD (AQP4+NMOSD) and those with multiple sclerosis (MS) in a retrospective cohort study. Brain volume was calculated with statistical parametric mapping-12.

resultsWe enrolled 36 patients with AQP4+NMOSD and 60 with MS. Patients with NMOSD were older and had a higher Kurtzke's expanded disability status scale score at baseline MRI compared with those with MS. Disease duration, annual relapse rate and intervals from the last attack and from disease-modifying drugs initiation were not significantly different between the two groups. Lower normalised lesion volume and higher normalised white matter volume were found in patients with NMOSD compared with those with MS at baseline MRI. However, the annualised atrophy rate of normalised brain volume was similar between the NMOSD (median 0.47; IQR 0.75; p=0.49) and MS (median 0.46; IQR 0.84) groups. After adjustment of age and the presence of clinical relapse, no differences of the annualised atrophy rate of normalised brain volume also were found for NMOSD and MS. Patients with AQP4+NMOSD with long cord lesion showed higher annualised atrophy rate of normalised grey matter volume compared with those without long cord lesion.

conclusionsSilent progression of brain atrophy was present in patients with AQP4+NMOSD, as shown in patients with MS, even in the clinically inactive age-matched cases. Subclinical dying back degeneration may explain the brain atrophy in patients with AQP4 +NMOSD.

Indexed as

Aquaporin 4AtrophyAutoantibodiesBrainCohort StudiesFemaleGray MatterHumansLongitudinal StudiesMagnetic Resonance ImagingMaleMultiple SclerosisNeuromyelitis OpticaRetrospective StudiesAquaporin 4Autoantibodies

Identifiers

PMID34362853
PMCPMC8685614
OpenAlexW3191362936

What OpenQuestion holds

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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.