Evidence map›Paper›PMID 36762496›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2023

Association of Anti-CCAR1 Autoantibodies With Decreased Cancer Risk Relative to the General Population in Patients With Anti-Transcriptional Intermediary Factor 1γ-Positive Dermatomyositis.

David Fiorentino, Christopher A Mecoli, Tak Igusa, Jemima Albayda, Julie J Paik, Eleni Tiniakou, Brittany Adler, Andrew L Mammen, Ami A Shah, Antony Rosen and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.1field-weighted citation impact, top 2% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Autoantibodies as biomarkers of cancer risk in dermatomyositis.JID innovations : skin science from molecules to population health · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Malignancy in Idiopathic Inflammatory Myopathies: Recent Insights.Clinical reviews in allergy & immunology · 2025
    Review
  8. Article
  9. Review
  10. Epidemiology of myositis.Current opinion in rheumatology · 2025
    Review
  11. Review
  12. Cancer in connective tissue disease.Frontiers in immunology · 2025
    Review
  13. Review
  14. Article
  15. Review
  16. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 2 countries.

David Fiorentino *Department of Dermatology, Stanford University School of Medicine, Redwood City, California.
Christopher A Mecoli *Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0002-1429-8392
Tak IgusaWhiting School of Engineering, Johns Hopkins University, Baltimore, Maryland.
Jemima AlbaydaDepartment of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0002-8030-9504
Julie J PaikDepartment of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0001-8436-1601
Eleni TiniakouDepartment of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0003-4749-870X
Brittany AdlerDepartment of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Andrew L MammenDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, and Muscle Disease Unit, Laboratory of Muscle Stem Cells and Gene Regulation, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland.ORCID 0000-0003-3732-3252
Ami A ShahDepartment of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Antony RosenDepartment of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Lisa Christopher-StineDepartment of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0002-7150-7306
Livia Casciola-RosenDepartment of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0002-4172-1539
Johns Hopkins University · USSeirei Christopher University · JP

Funding

Sample Processing and Immunoassay Research CoreP30AR070254 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI Antony Rosen · 2016 to 2026
$8.9M
Autoantibodies Define Scleroderma Subgroups with Distinct Relationships to CancerR01AR073208 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI LIVIA A CASCIOLA-ROSEN, Ami Aalok Shah · 2018 to 2026
$5.2M
Harnessing multivariate patient- and population-level disease trajectories to predict major clinical events in sclerodermaK24AR080217 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI Ami Aalok Shah · 2022 to 2026
$847k
RNA: Polymerase III specific CD8+ T cells: a mechanistic insight into cancer-induced autoimmunity in sclerodermaK08AR077732 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TINIAKOU, ELENI · 2021 to 2025
$794k
Optimizing the Approach to Identify Cancer-Associated MyositisK23AR075898 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI MECOLI, CHRISTOPHER · 2019 to 2023
$773k
NIAMS NIH HHS K08 AR077732NIAMS NIH HHS K23 AR075898NIAMS NIH HHS K24 AR080217NIAMS NIH HHS P30 AR070254NIAMS NIH HHS R01 AR073208
6 · The paper itself

Abstract

objectiveTo describe the disease specificity, clinical phenotype, and risk of cancer in dermatomyositis (DM) patients with autoantibodies against cell division cycle and apoptosis regulator protein 1 (anti-CCAR1).

methodsThe frequency of anti-CCAR1 autoantibodies was measured by enzyme-linked immunosorbent assay in the serum of DM patients from 2 independent cohorts (Johns Hopkins and Stanford), with patients with several other rheumatic diseases and healthy controls used as comparators. Clinical features and the risk of cancer incidence relative to that in the general population were determined in anti-CCAR1-positive DM patients.

resultsAnti-CCAR1 antibodies were significantly associated with anti-transcriptional intermediary factor 1γ (anti-TIF1γ) antibodies present in the serum of patients with DM: 80 (32%) of 252 anti-TIF1γ-positive DM patients versus 14 (8%) of 186 anti-TIF1γ-negative DM patients were positive for anti-CCAR1 antibodies (P < 0.001). Anti-CCAR1 antibodies were not detected in any of the 32 serum samples from healthy controls, and were present at very low frequencies in the sera of patients with other rheumatic diseases: 1 (2.3%) of 44 patients with anti-hydroxymethylglutaryl-coenzyme A reductase-positive necrotizing myopathy, 1 (2.3%) of 44 patients with inclusion body myositis, and 3 (6.5%) of 46 patients with systemic lupus erythematosus were positive for anti-CCAR1 antibodies. Upon examining data on occurrence of cancer from the onset of DM onward, the observed number of cancers diagnosed in anti-TIF-1γ-positive DM patients was significantly greater than expected in both cohorts, with a standardized incidence ratio (SIR) of 3.49 (95% confidence interval [95% CI] 2.39-4.92) in the Johns Hopkins cohort and a SIR of 4.54 (95% CI 3.04-6.52) in the Stanford cohort (each P < 0.001). DM patients who were both anti-TIF1γ positive and anti-CCAR1 positive had lower SIRs for cancer, with a SIR of 1.78 (95% CI 0.77-3.51) (P = 0.172) in the Johns Hopkins cohort and a SIR of 1.61 (95% CI 0.44-4.13) (P = 0.48) in the Stanford cohort.

conclusionAnti-CCAR1 autoantibodies are specific for anti-TIF1γ-positive DM. Their presence in anti-TIF1γ-positive patients attenuates the risk of cancer to a level comparable to that seen in the general population.

Indexed as

DermatomyositisNeoplasmsRheumatic DiseasesAutoantibodiesHumansMediation AnalysisAutoantibodies

Identifiers

PMID36762496
PMCPMC10313743
OpenAlexW4319826531

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.