Evidence map›Paper›PMID 39080801›Full record

ArticleArthritis research & therapy2024

Expression of CD163 and major histocompatibility complex class I as diagnostic markers for idiopathic inflammatory myopathies.

Byeongzu Ghang, So Hye Nam, Wonho Choi, Hwa Jung Kim, Jungsun Lee, Doo-Ho Lim, Soo Min Ahn, Ji Seon Oh, Seokchan Hong, Yong-Gil Kim and 4 more

Abstract read
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Article in Arthritis research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. A quantitative redox proteome of the human muscle response to exercise.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Review
  4. The Role of C/EBP-Homologous Protein in Idiopathic Inflammatory Myopathies.Journal of cellular and molecular medicine · 2025
    Article
4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Byeongzu GhangDivision of Rheumatology, Jeju National University School of Medicine, Jeju National University Hospital, Jeju, Republic of Korea.
So Hye NamDivision of Rheumatology, Department of Internal Medicine, Keimyung University School of Medicine, Daegu, South Korea.
Wonho ChoiDivision of Rheumatology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Hwa Jung KimDepartment of Clinical Epidemiology and Biostatistics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Jungsun LeeDivision of Rheumatology, Department of Internal Medicine, Seoul Veterans Hospital, Seoul, Republic of Korea.
Doo-Ho LimDivision of Rheumatology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Republic of Korea.
Soo Min AhnDivision of Rheumatology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Ji Seon OhDivision of Rheumatology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Seokchan HongDivision of Rheumatology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Yong-Gil KimDivision of Rheumatology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Chang-Keun LeeDivision of Rheumatology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Jinseok KimDivision of Rheumatology, Jeju National University School of Medicine, Jeju National University Hospital, Jeju, Republic of Korea.
Bin YooDivision of Rheumatology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea. byoo@amc.seoul.kr.
Soo Jeong NamDivision of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea. soojeong_nam@amc.seoul.kr.

Funding

Jeju National University Hospital 2021-39
6 · The paper itself

Abstract

backgroundTo develop an inflammation-related immunohistochemistry marker-based algorithm that confers higher diagnostic ability for idiopathic inflammatory myopathies (IIMs) than IIM-related histopathologic features.

methodsMuscle biopsy tissues from 129 IIM patients who met the 2017 EULAR/ACR criteria and 73 control tissues from patients with non-inflammatory myopathies or healthy muscle specimens were evaluated for histological features and immunostaining results of CD3, CD4, CD8, CD20, CD68, CD163, MX1, MHC class I, MHC class II, and HLA-DR. Diagnostic algorithms for IIM were developed based on the results of the classification and regression tree (CART) analysis, which used immunostaining results as predictor variables for classifying patients with IIMs.

resultsIn the analysis set (IIM, n = 129; control, n = 73), IIM-related histopathologic features had a diagnostic accuracy of 87.6% (sensitivity 80.6%; specificity 100.0%) for IIMs. Notably, muscular expression of CD163 (99.2% vs. 20.8%, p < 0.001) and MHC class I (87.6% vs. 23.1%, p < 0.001) was significantly higher in the IIM group than in controls. Based on the CART analysis results, we developed an algorithm combining CD163 and MHC class I expression that conferred a diagnostic accuracy of 95.5% (sensitivity 96.1%; specificity 94.5%). In addition, our algorithm was able to correctly diagnose IIM in 94.1% (16/17) of patients who did not meet the 2017 EUALR/ACR criteria but were diagnosed as having IIMs by an expert physician.

conclusionsCombination of CD163 and MHC class I muscular expression may be useful in diagnosing IIMs.

Indexed as

Antigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersHistocompatibility Antigens Class IMyositisReceptors, Cell SurfaceAdultAgedAlgorithmsCD163 AntigenFemaleHumansImmunohistochemistryMaleMiddle AgedMuscle, SkeletalAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCD163 AntigenHistocompatibility Antigens Class IReceptors, Cell SurfaceCD163 antigenHistocompatibility antigens class IImmunohistochemistryMyositis

Identifiers

PMID39080801
PMCPMC11290050

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LicenceCC BY-NC-ND
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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.