Evidence map›Paper›PMID 41258085›Full record

ArticleJournal of neurology2025

Severe attacks and worse prognosis in patients with late-onset neuromyelitis optica spectrum disorder highlight the need for early highly effective treatment.

Rui Wang, Xiaofei Wang, Ziyan Shi, Lingyao Kong, Qin Du, Ying Zhang, Hongxi Chen, Nana Zhang, Yangyang Zhang, Hongyu Zhou

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Article in Journal of neurology, 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. Article
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4 · The record

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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

10 authors.

Rui Wang *Department of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China.
Xiaofei Wang *Department of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China.
Ziyan ShiDepartment of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China.
Lingyao KongDepartment of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China.
Qin DuDepartment of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China.
Ying ZhangDepartment of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China.
Hongxi ChenDepartment of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China.
Nana ZhangDepartment of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China.
Yangyang ZhangDepartment of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China.
Hongyu ZhouDepartment of Neurology, West China Hospital, Sichuan University, No. 37 Guoxue Road, Chengdu, 610041, Sichuan, People's Republic of China. zhouhy@scu.edu.cn.ORCID http://orcid.org/0000-0002-7637-1305

Funding

National Natural Science Foundation of China 82201494National Natural Science Foundation of China 82471376
6 · The paper itself

Abstract

BACKGROUND AND

objectivesPatients with late-onset neuromyelitis optica spectrum disorder (LO-NMOSD) have a worse prognosis than those with early onset NMOSD (EO-NMOSD), with limited immunotherapy data for patients with LO-NMOSD. We compared the efficacy of moderate and highly effective treatments for patients with LO-NMOSD.

methodsWe retrospectively included 695 aquaporin-4 immunoglobulin G-positive patients with EO-NMOSD (onset at age < 50 years) and LO-NMOSD (onset at age ≥ 50 years), comparing their clinical and immunologic features. Patients with LO-NMOSD were divided into two subgroups: one using moderately effective treatments, and one using highly effective treatments, focusing on relapse rates and prognostic outcomes.

resultsIn total, 208 (29.9%) patients had LO-NMOSD. The median disease duration was 4.21 years for the LO-NMOSD group and 7.33 years for the EO-NMOSD group. Patients with LO-NMOSD had a higher proportion of myelitis (47.6% vs. 31.2%) and higher Expanded Disability Status Scale (EDSS) scores at first attack [false discovery rate (FDR) corrected p = 0.001]. Severe attacks (EDSS ≥ 6) and motor disability at last follow-up was less common in EO-NMOSD. No difference in visual disability was observed between the two groups at last follow-up. Among patients with LO-NMOSD, 170 (81.7%) received moderately effective treatment and 38 (18.3%) received highly effective treatment. Patients using moderately effective treatments had a lower relapse-free rate than those using highly effective treatments (67.1% vs. 94.7%). DISCUSSION: Patients with LO-NMOSD had more severe attacks and worse prognoses than those with EO-NMOSD. Patients with LO-NMOSD may choose highly effective treatments as a first-line therapy.

Indexed as

Neuromyelitis OpticaAdultAgedAge of OnsetAquaporin 4FemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesSeverity of Illness IndexTreatment OutcomeAQP4 protein, humanAquaporin 4Highly effective treatmentImmunosuppressantsLate-onsetNeuromyelitis optica spectrum disorderRelapse

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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.