Evidence map›Paper›PMID 34175923›Full record

ArticleRheumatology (Oxford, England)2022

Serological abnormalities that predict progression to systemic autoimmune rheumatic diseases in antinuclear antibody-positive individuals.

Carolina Muñoz-Grajales, Stephenie D Prokopec, Sindhu R Johnson, Zahi Touma, Zareen Ahmad, Dennisse Bonilla, Linda Hiraki, Arthur Bookman, Paul C Boutros, Andrzej Chruscinski and 1 more

Open access · greenAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. REDEFINING AUTOIMMUNE DISEASES: THE OPPORTUNITY FOR PRECISION AND PREVENTION.Transactions of the American Clinical and Climatological Association · 2025
    Review
  6. Article
  7. Article
  8. Advanced Autoantibody Testing in Systemic Sclerosis.Diagnostics (Basel, Switzerland) · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Review
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

11 authors at 4 institutions in 3 countries.

Carolina Muñoz-GrajalesDepartment of Immunology, Faculty of Medicine, University of Toronto.
Stephenie D ProkopecOntario Institute for Cancer Research.
Sindhu R JohnsonToronto Scleroderma Program, Division of Rheumatology, Toronto Western and Mount Sinai Hospitals.
Zahi ToumaDepartment of Medicine, University of Toronto, Faculty of Medicine.ORCID 0000-0001-5177-2076
Zareen AhmadToronto Scleroderma Program, Division of Rheumatology, Toronto Western and Mount Sinai Hospitals.
Dennisse BonillaSchroeder Arthritis Institute, Krembil Research Institute, University Health Network.
Linda HirakiDivision of Rheumatology, Hospital for Sick Children and Department of Paediatrics, University of Toronto.ORCID 0000-0002-6690-8148
Arthur BookmanDepartment of Medicine, University of Toronto, Faculty of Medicine.
Paul C BoutrosDepartment of Human Genetics, Institute for Precision Health.
Andrzej ChruscinskiMulti-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Joan WitherDepartment of Immunology, Faculty of Medicine, University of Toronto.ORCID 0000-0001-5961-9228
University Health Network · CAUniversity of Toronto · CAOntario Institute for Cancer Research · CAUniversity of California, Los Angeles · US

Funding

CIHR FRN 159563
6 · The paper itself

Abstract

objectiveWe investigated the autoantibody (autoAb) profiles in ANA+ individuals lacking systemic autoimmune rheumatic disease (SARD) and early SARD patients to determine the key differences between these groups and identify factors that are associated with an increased risk of symptomatic progression within the next 2 years in ANA+ individuals.

methodsUsing custom antigen (Ag) microarrays, 144 IgM and IgG autoAbs were surveyed in 84 asymptomatic and 123 symptomatic (48 UCTD and 75 SARD patients) ANA+ individuals. AutoAbs were compared in ANA+ individuals lacking a SARD diagnosis with ≥2 years follow-up (n = 52), including all those who demonstrated progression (n = 14) during this period, with changes over time assessed in a representative subset.

resultsWe show that ANA+ individuals have autoAb to many self-Ags that are not being captured by current screening techniques and very high levels of these autoAbs are predominantly restricted to early SARD patients, with SLE patients displaying reactivity to many more autoAgs than the other groups. In general, the symptoms that developed in progressors mirrored those seen in SARD patients with similar patterns of autoAbs. Only anti-Ro52 Abs were found to predict progression (positive predictive value 46%, negative predictive value 89%). Surprisingly, over 2 years of follow-up the levels of autoAbs remained remarkably stable regardless of whether individuals progressed or not.

conclusionOur findings strongly argue that development of assays with an expanded set of auto-Ags and enhanced dynamic range would improve the diagnostic and prognostic ability of autoAb testing.

Indexed as

AdultAntibodies, AntinuclearAutoimmune DiseasesDisease ProgressionFemaleHumansMaleMiddle AgedPredictive Value of TestsRheumatic DiseasesYoung AdultAntibodies, Antinuclearantinuclear antibodiesmicroarray analysisrheumatic diseasesRo52 antigenSLE

Identifiers

PMID34175923
PMCPMC8889298
OpenAlexW3173204822

What OpenQuestion holds

Textmetadata
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.