# Association of clinical features and myositis-specific antibodies in idiopathic inflammatory myopathy: a retrospective study from southern China

**Authors:** Can Li, Yushi Zheng, Yu Zhang, Yujin Ye, Hui Zhang, Niansheng Yang, Shuang Wang

PMC · DOI: 10.3389/fimmu.2025.1674437 · 2025-11-06

## TL;DR

This study from southern China shows that specific myositis antibodies are linked to distinct clinical features and outcomes in inflammatory muscle disease patients.

## Contribution

The study provides a detailed analysis of MSA profiles and their clinical correlations in a southern Chinese IIM cohort.

## Key findings

- Anti-MDA5 and anti-ARS antibodies are strongly associated with interstitial lung disease and distinct clinical features.
- Anti-TIF1-γ and anti-Mi-2 antibodies are most common in IIM patients with malignancies, especially nasopharyngeal carcinoma.
- Anti-MDA5 positivity is linked to a higher risk of rapidly progressive ILD and lower 3-month survival rates.

## Abstract

This study aimed to investigate the profiles of myositis-specific autoantibodies (MSA) and their correlation with distinct clinical features in patients with idiopathic inflammatory myopathy (IIM) in southern China. We retrospectively analyzed the medical records of 208 IIM patients, collecting data on their demographic variables, clinical manifestations, comorbidities, and MSA test results. Of the 208 patients, 185 were positive for MSAs. 69 patients were anti-MDA5 positive, 61 patients were anti-ARS positive followed by anti-SRP (34), anti-TIF1-γ (26), anti-Mi-2β (10), anti-NXP2 (10), anti-HMGCR (9), anti-Mi-2α (6), anti-cN-1A (6), and anti-SAE1 (1). Distinct clinical phenotypes were strongly associated with specific antibodies. Anti-MDA5 positive patients had shorter disease duration, less muscle involvement, but higher rates of rash, alopecia, arthritis, fever, and ILD with poorer prognosis. Anti-ARS positive patients had longer disease duration, mechanic’s hands, arthritis, fever, and ILD, but better prognosis. Both anti-MDA5 and anti-ARS antibodies were independent risk factors for developing ILD. Anti-TIF1-γ and anti-Mi-2 were most detected in IIM patients combined with malignancies, and nasopharyngeal carcinoma was the most common malignant tumor. Furthermore, hyperlipidemia and elevated cardiac biomarkers were frequently observed, particularly in patients positive for anti-SRP. The 3-month survival rate for anti-MDA5 positive patients was 87.8%, with all deaths attributed to rapidly progressive-ILD (RP-ILD). In contrast, other antibody positive patients had a 100% survival rate. This comprehensive analysis of a southern Chinese IIM cohort underscores that MSA profiles can effectively stratify patients into clinically distinct subgroups, which is crucial for predicting specific organ involvement, prognosis, and developing tailored treatment strategies.

## Linked entities

- **Proteins:** IFIH1 (interferon induced with helicase C domain 1), RIEG2 (Rieger syndrome 2), UCN2 (urocortin 2), TRIM33 (tripartite motif containing 33), CHD4 (chromodomain helicase DNA binding protein 4), MORC3 (MORC family CW-type zinc finger 3), HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase), CHD3 (chromodomain helicase DNA binding protein 3), NT5C1A (5'-nucleotidase, cytosolic IA), SAE1 (SUMO1 activating enzyme subunit 1)
- **Diseases:** idiopathic inflammatory myopathy (MONDO:0600023), interstitial lung disease (MONDO:0015925), nasopharyngeal carcinoma (MONDO:0015459), hyperlipidemia (MONDO:0021187)

## Full-text entities

- **Genes:** MORC3 (MORC family CW-type zinc finger 3) [NCBI Gene 23515] {aka NXP2, ZCW5, ZCWCC3}, TRIM33 (tripartite motif containing 33) [NCBI Gene 51592] {aka DDH4, ECTO, PTC7, RFG7, TF1G, TIF1G}, CHD3 (chromodomain helicase DNA binding protein 3) [NCBI Gene 1107] {aka Mi-2a, Mi2-ALPHA, SNIBCPS, ZFH}, HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156] {aka LDLCQ3, LGMDR28, MYPLG}, SAE1 (SUMO1 activating enzyme subunit 1) [NCBI Gene 10055] {aka AOS1, HSPC140, SUA1, UBLE1A}, NT5C1A (5'-nucleotidase, cytosolic IA) [NCBI Gene 84618] {aka CN-I, CN-IA, CN1, CN1A, CNI}, CHD4 (chromodomain helicase DNA binding protein 4) [NCBI Gene 1108] {aka CHD-4, Mi-2b, Mi2-BETA, SIHIWES}, IFIH1 (interferon induced with helicase C domain 1) [NCBI Gene 64135] {aka AGS7, Hlcd, IDDM19, IMD95, MDA-5, MDA5}, RIEG2 (Rieger syndrome 2) [NCBI Gene 6012] {aka ARS, RGS2}
- **Diseases:** ILD (MESH:D017563), RP-ILD (MESH:C538458), arthritis (MESH:D001168), alopecia (MESH:D000505), progressive (MESH:D018450), rash (MESH:D005076), nasopharyngeal carcinoma (MESH:D000077274), malignancies (MESH:D009369), IIM (MESH:D009220), deaths (MESH:D003643), fever (MESH:D005334), muscle involvement (MESH:C566343), hyperlipidemia (MESH:D006949)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12631342/full.md

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Source: https://tomesphere.com/paper/PMC12631342