Evidence map›Paper›PMID 41080932›Full record

ArticleFrontiers in medicine2025

Predictive models for non-response to conventional treatment in polymyositis and dermatomyositis.

Bo Zang, Lishan Xu, Qixuan Liu, Yuan Yao, Hua Li, Dacheng Li, Lingwei Liu, Ruiwen Liang, Xinyue Zhao, Peng Zhao and 2 more

Abstract read
In one paragraph

Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Bo Zang *Department of Rheumatology and Immunology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Lishan Xu *Department of Rheumatology and Immunology, Liaocheng People's Hospital, Liaocheng, Shandong, China.
Qixuan LiuGraduate Group of Epidemiology, University of California, Davis, Davis, CA, United States.
Yuan YaoDepartment of Rheumatology and Immunology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Hua LiDepartment of Rheumatology and Immunology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Dacheng LiDepartment of Nuclear Medicine, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Lingwei LiuDepartment of Geriatrics, Shengli Oilfield Central Hospital, Dongying, Shandong, China.
Ruiwen LiangDepartment of Rheumatology and Immunology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Xinyue ZhaoDepartment of Rheumatology and Immunology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Peng ZhaoDepartment of Pathology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Chunli XuDepartment of Neurology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Bin LiuDepartment of Rheumatology and Immunology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Polymyositis (PM) and dermatomyositis (DM) are the major subtypes of idiopathic inflammatory myopathies with heterogeneous treatment responses. This study aimed to develop a predictive model for identifying PM/DM patients who are non-responsive to conventional therapy by assessing a range of diagnostic tools to guide individualized treatment. Methods: Patients with PM/DM from two medical centers (January 2010-December 2024) were included. Baseline and 12-week post-treatment clinical data were collected. Logistic regression was employed to develop both comprehensive and non-invasive predictive models. Model performance was validated using the area under the receiver operating characteristic curve (AUC) in internal and external test sets. Results: The Qingdao cohort comprised 84 patients (age 57.7 ± 1.5 years; 54 females [62.5%]; DM = 53, PM = 31) and the Liaocheng cohort included 22 patients (age 56.4 ± 3.8 years; 15 females [68.2%]; DM = 13, PM = 9). Gender, mSUVmax, and muscle bundle atrophy were identified as independent predictive factors. The comprehensive model achieved an AUC of 0.900 (95% confidence intervals [CI]: 0.813-1.009) in the training set, demonstrating superior diagnostic performance compared to the non-invasive model. The non-invasive model yielded AUCs of 0.857 (95% CI: 0.766-0.972), 0.742 (95% CI: 0.599-0.984), and 0.765 (95% CI: 0.632-0.987) in the training, internal test, and external test sets, respectively, indicating broader applicability across different cohorts. Both models showed good discrimination and calibration, and decision curve analysis further confirmed their clinical value. Discussion: These findings suggest that predictive models based on clinical, pathological, and imaging features can effectively identify PM/DM patients who are non-responsive to conventional therapy, potentially providing a tool for personalized treatment.

Indexed as

FDG-PET/CTidiopathic inflammatory myopathiesmuscle biopsiespersonalized treatmentpredictive model

Identifiers

PMID41080932
PMCPMC12511047

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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.