Evidence map›Paper›PMID 28365584›Full record

ArticleThe Journal of rheumatology2017

Antifibrillarin Antibodies Are Associated with Native North American Ethnicity and Poorer Survival in Systemic Sclerosis.

Carolina Mejia Otero, Shervin Assassi, Marie Hudson, Maureen D Mayes, Rosa Estrada-Y-Martin, Claudia Pedroza, Tingting W Mills, Jennifer Walker, Murray Baron, Wendy Stevens and 8 more

Abstract read
In one paragraph

Article in The Journal of rheumatology, 2017. 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
1.9field-weighted citation impact, top 16% 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, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Systemic Sclerosis-Specific Antibodies: Novel and Classical Biomarkers.Clinical reviews in allergy & immunology · 2023
    Article
  6. Advanced Autoantibody Testing in Systemic Sclerosis.Diagnostics (Basel, Switzerland) · 2023
    Review
  7. Article
  8. Article
  9. Fibrillarin antibodies in systemic sclerosis.Archives of rheumatology · 2022
    Article
  10. Article
  11. Observational
  12. Overall mortality.Journal of scleroderma and related disorders · 2021
    Article
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

18 authors at 8 institutions in 3 countries.

Carolina Mejia Otero
Shervin Assassi
Marie Hudson
Maureen D Mayes
Rosa Estrada-Y-Martin
Claudia Pedroza
Tingting W Mills
Jennifer Walker
Murray Baron
Wendy Stevens
Susanna M Proudman
Mandana Nikpour
Sonal Mehra
Mianbo Wang
Marvin J Fritzler
Canadian Scleroderma Research Group
Australian Scleroderma Cohort Study
Genetics versus Environment in Scleroderma Outcome Study
McGill University · CAThe University of Texas Health Science Center at Houston · USCenter for Clinical Research (United States) · USFlinders Medical Centre · AUSt Vincent's Hospital · AUThe University of Texas at Austin · USUniversity of Adelaide · AUUniversity of Melbourne · AU

Funding

Two-Stage Genome-Wide Association Study in Systemic SclerosisR01AR055258 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MAYES, MAUREEN MAUREEN · 2008 to 2012
$5.9M
Molecular Markers for Progression of Pulmonary Fibrosis in Systemic SclerosisK23AR061436 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ASSASSI, SHERVIN · 2011 to 2014
$494k
NIAMS NIH HHS K23 AR061436NIAMS NIH HHS R01 AR055258
6 · The paper itself

Abstract

objectiveTo examine the clinical correlates and survival in patients with antifibrillarin antibodies (AFA) in a large international study population consisting of well-characterized systemic sclerosis (SSc) cohorts from Canada, Australia, and the United States.

methodsBaseline clinical data from the prospective cohorts (Canadian Scleroderma Research Group, the Australian Scleroderma Cohort Study, and the American Genetics versus Environment in Scleroderma Outcome Study) were investigated. Clinical variables were harmonized and sera were tested for AFA using a commercially available SSc profile line immunoassay, regardless of the immunofluorescence staining pattern. Association of demographic and clinical features with AFA was investigated by logistic or linear regression. Further, a survival analysis was performed by Cox regression analysis.

resultsA total of 1506 patients with SSc with complete serological profiles were included in the study. Fifty-two patients (3.5%) had antibodies detected against fibrillarin. Patients of African descent and Native North American ethnicity were more likely to be AFA-positive compared with other ethnicities. After adjustment for demographic factors, diffuse involvement, and intestinal bacterial overgrowth requiring antibiotics, gastrointestinal reflux disease showed a trend for association with AFA. Further, AFA positivity was associated with shorter survival independently of demographic factors and disease type (HR 1.76, 95% CI 1.11-2.79, p = 0.016).

conclusionIn this large multinational SSc cohort, AFA was associated with Native American ethnicity and was an independent predictor of mortality.

Indexed as

AdultAgedAutoantibodiesChromosomal Proteins, Non-HistoneFemaleHumansIndians, North AmericanMaleMiddle AgedProspective StudiesScleroderma, SystemicSurvival AnalysisSurvival RateAutoantibodiesChromosomal Proteins, Non-HistonefibrillarinANTIFIBRILLARIN ANTIBODIESAUTOIMMUNITYSYSTEMIC SCLEROSIS

Identifiers

PMID28365584
PMCPMC5457664
OpenAlexW2598667327

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.