Evidence map›Paper›PMID 41066347›Full record

ArticlePloS one2025

Comparative study of Japanese nationwide epidemiological studies of myasthenia gravis using datasets of 2006 and 2018.

Hiroaki Yoshikawa, Yumi Adachi, Yosikazu Nakamura, Nagato Kuriyama, Hiroyuki Murai, Yoshiko Nomura, Yasunari Sakai, Kazuo Iwasa, Yutaka Furukawa, Makoto Matsui and 2 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Hiroaki YoshikawaHealth Service Center, Kanazawa University, Kanazawa, Ishikawa, Japan.ORCID https://orcid.org/0000-0002-6350-5183
Yumi AdachiHealth Service Center, Kanazawa University, Kanazawa, Ishikawa, Japan.
Yosikazu NakamuraPublic Health Center, Utsunomiya City, Tochigi, Japan.
Nagato KuriyamaShizuoka Graduate University of Public Health, Shizuoka City, Shizuoka, Japan.
Hiroyuki MuraiDepartment of Neurology, School of Medicine, International University of Health and Welfare, Narita, Chiba, Japan.
Yoshiko NomuraYoshiko Nomura Neurological Clinic for Children, Bunkyo-ku, Tokyo, Japan.
Yasunari SakaiDepartment of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.ORCID https://orcid.org/0000-0002-5747-8692
Kazuo IwasaIshikawa Prefectural Nursing University, Kahoku, Ishikawa, Japan.
Yutaka FurukawaNHO Kanazawa Medical Center, Kanazawa, Japan.
Makoto MatsuiDepartment of Neurology, Houju Memorial Hospital, Nomi, Ishikawa, Japan.
Satoshi KuwabaraDepartment of Neurology, Graduate School of Medicine, Chiba University, Chiba City, Chiba, Japan.
Taskforce of Research that Aims to Contribute to Improving the Medical Level of Intractable Diseases and Neuroimmune Patients’ Quality of Life

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to identify changes in the clinical presentation and treatment patterns of myasthenia gravis (MG) in Japan by comparing data from nationwide epidemiological surveys conducted in 2006 and 2018.

methodsWe analyzed data from nationwide epidemiological surveys of MG performed across Japan in 2006 (n = 729) and 2018 (n = 1,357). Both surveys adhered to the Survey Manual of Study on Continuous Epidemiological Data Collection of Intractable Diseases established by the Ministry of Health, Labour, and Welfare. We compared the following variables between the two-time points: age of onset, gender distribution, initial symptoms, anti-acetylcholine receptor antibody (AChRAb) status, physiological test results (repetitive nerve stimulation test, edrophonium test), Myasthenia Gravis Foundation of America (MGFA) Clinical Classification, Myasthenia Gravis Activities of Daily Living Profile (MG-ADL) score, and treatment modalities.

resultsOur analysis revealed a significantly older age of onset in the 2018 cohort compared to 2006. The MGFA Clinical Classification was higher in 2018, and bulbar weakness was more frequently reported as an initial symptom. Conversely, the occurrence of myasthenic crisis and current MG-ADL scores were lower in 2018. Regarding treatment, the utilization of tacrolimus, plasma exchange (PE), and intravenous immunoglobulin (IVIg) significantly increased between 2006 and 2018. In contrast, the rates of thymectomy and both maximum and current oral steroid dosages decreased during this period.

conclusionThese findings underscore notable shifts in the clinical characteristics and, particularly, the treatment strategies for MG in Japan over the twelve-year interval. This information is crucial for informing future patient care protocols and healthcare policy development in the management of MG. We emphasize the importance of conducting regular nationwide epidemiological surveys to monitor the evolving landscape of MG and its treatment continuously.

Indexed as

Myasthenia GravisActivities of Daily LivingAdolescentAdultAgedAged, 80 and overAge of OnsetChildEast Asian PeopleFemaleHumansImmunoglobulins, IntravenousJapanMaleMiddle AgedPlasma ExchangeImmunoglobulins, Intravenous

Identifiers

PMID41066347
PMCPMC12510604

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.