Evidence map›Paper›PMID 39881842›Full record

ArticleTherapeutic advances in musculoskeletal disease2025

Identification of clinical subgroups in anti-SRP positive immune-mediated necrotizing myopathy patients using cluster analysis.

Beibei Cui, Hongjiang Liu, Ruiting Liu, Geng Yin, Qibing Xie

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

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1citing papers in PubMed
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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Beibei CuiDepartment of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0002-5870-2369
Hongjiang LiuDepartment of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, China.
Ruiting LiuDepartment of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, China.
Geng YinHealth Management Center, General Practice Medical Center, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu, 610041, China.
Qibing XieDepartment of Rheumatology and Immunology, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu, 610041, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Anti-signal recognition particle immune-mediated necrotizing myopathy (anti-SRP IMNM) is a rare autoimmune disorder characterized by muscle weakness and necrosis. Identifying clinical subgroups within this patient population could facilitate the management of the disease. Objectives: To identify distinct clinical subgroups of anti-SRP IMNM patients. Design: A retrospective study was conducted on anti-SRP IMNM patients treated at West China Hospital of Sichuan University between January 2010 and October 2023. Methods: Clinical data were collected. Unsupervised cluster analysis was conducted to classify patients into distinct subgroups based on their clinical features. Statistical analyses were performed to compare the clinical characteristics and outcomes among the identified clusters. Results: A total of 116 patients were included in the study, and 3 distinct clinical subgroups were identified: Cluster 3 (acute), Cluster 2 (subacute), and Cluster 1 (poor prognosis). Patients in Cluster 3 exhibited a short disease course (median 3 months), severe muscle weakness (78.38% with Medical Research Council (MRC) score ⩽3), high muscle enzyme levels, and a good response to treatment. Cluster 2 patients were younger (mean age 45.83 years), had a longer disease course (median 6.5 months), milder muscle damage, and lower autoantibody titers. Cluster 1 patients were older (mean age 58.10 years), predominantly male (70.97%), and had higher incidences of interstitial lung disease (70.97%) and cardiac injury (45.16%). In Cluster 1, 16.13% of cases were refractory, and the relapse rate was 38.71%, which was significantly higher compared to the other two clusters. Conclusion: This study highlights the clinical heterogeneity among anti-SRP IMNM patients and identifies three distinct clinical subgroups with unique characteristics. These findings provide insights for personalized management.

Indexed as

anti-SRP autoantibodiesimmune-mediated necrotizing myopathyprognosisunsupervised cluster analysis

Identifiers

PMID39881842
PMCPMC11775970

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