Evidence map›Paper›PMID 41869361›Full record

ArticleFrontiers in immunology2026

The clinical, serological and myopathological features of a cohort of Chinese patients with inclusion body myositis: a single center analysis.

Hongyan Qiu, Shouzheng Yang, Xuejun Guo, Yinglin Leng, Yawen Zhao, Meng Yu, Yiming Zheng, Lingchao Meng, He Lv, Jianwen Deng and 4 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Hongyan Qiu *Department of Neurology, Peking University First Hospital, Beijing, China.
Shouzheng Yang *Department of Neurology, Peking University First Hospital, Beijing, China.
Xuejun Guo *Department of Neurology, Peking University First Hospital, Beijing, China.
Yinglin LengDepartment of Neurology, Peking University First Hospital, Beijing, China.
Yawen ZhaoDepartment of Neurology, Peking University First Hospital, Beijing, China.
Meng YuDepartment of Neurology, Peking University First Hospital, Beijing, China.
Yiming ZhengDepartment of Neurology, Peking University First Hospital, Beijing, China.
Lingchao MengDepartment of Neurology, Peking University First Hospital, Beijing, China.
He LvDepartment of Neurology, Peking University First Hospital, Beijing, China.
Jianwen DengDepartment of Neurology, Peking University First Hospital, Beijing, China.
Wei ZhangDepartment of Neurology, Peking University First Hospital, Beijing, China.
Zhaoxia WangDepartment of Neurology, Peking University First Hospital, Beijing, China.
Yun YuanDepartment of Neurology, Peking University First Hospital, Beijing, China.
Qiang GangDepartment of Neurology, Peking University First Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: This study aimed to investigate the clinical, serological and myopathological features of Chinese patients with inclusion body myositis (IBM). Methods: This study retrospectively recruited patients diagnosed with IBM according to the 2024 European Neuromuscular Center (ENMC) criteria at Peking University First Hospital between 2004 and 2024. Clinical features, pathological changes and laboratory data were collected. Subgroups were analyzed by sex, dysphagia, anti-cN1A antibody status, and complement deposition. Results: Forty-three IBM patients (25 males) were included in this cohort. The mean age at onset was 54.9 ± 9.6 years old. All the patients developed weakness in hip flexion, and 81.4% of them with weakness in both knee extension and finger flexion. Dysphagia was reported in 17 patients (39.5%). Endomysial inflammation was observed in all the patients, and 79.1% with rimmed vacuoles, and 76.9% with mitochondrial abnormalities. Female patients more frequently developed dysphagia (P = 0.005) and neck flexion weakness (P < 0.001). Anti-cN1A antibody was positive in 20 patients (66.7%). Seropositive cases were associated with a later age of onset (P = 0.034). Complement deposition was observed in 77.4% of patients and was associated with more severe muscle weakness. Conclusion: This cohort of Chinese IBM patients suggested an earlier age at onset than previously reported. Hip flexors were most commonly affected. Female patients showed a higher frequency of dysphagia and neck flexor weakness. Our study reported a high frequency of complement deposition in muscle tissue. Complement deposition was associated with disease severity, suggesting a potential role of complement in the pathophysiology of IBM.

Indexed as

Myositis, Inclusion BodyAge of OnsetAutoantibodiesChinaDeglutition DisordersEast Asian PeopleFemaleHumansMaleMiddle AgedMuscle, SkeletalRetrospective StudiesAutoantibodiesanti-cN1A antibodycomplement depositiondysphagiaIBMinclusion body myositis

Identifiers

PMID41869361
PMCPMC12999901

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