Evidence map›Paper›PMID 26879356›Full record

ArticleThe Journal of rheumatology2016

Phenotypic Characterization of Juvenile Idiopathic Arthritis in African American Children.

Lauren Fitzpatrick, K Alaine Broadaway, Lori Ponder, Sheila T Angeles-Han, Kirsten Jenkins, Kelly Rouster-Stevens, Christina F Pelajo, Karen Conneely, Michael P Epstein, Jorge Lopez-Benitez and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of rheumatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The inequity of global healthcare in pediatric rheumatology.Best practice & research. Clinical rheumatology · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Lauren Fitzpatrick
K Alaine Broadaway
Lori Ponder
Sheila T Angeles-Han
Kirsten Jenkins
Kelly Rouster-Stevens
Christina F Pelajo
Karen Conneely
Michael P Epstein
Jorge Lopez-Benitez
Larry B Vogler
Sampath Prahalad
CARRA Registry Investigators
Emory University · USChildren's Healthcare of Atlanta · USTufts Children's Hospital · US

Funding

CARRA: Accelerating Toward an Evidence Based Culture in Pediatric RheumatologyRC2AR058934 · NIAMS · DUKE UNIVERSITY · PI ILOWITE, NORMAN T, SANDBORG, CHRISTY IRENE · 2009 to 2010
$6.8M
Segmental chromosome sharing in affected relatives with Juvenile ArthritisR01AR060893 · NIAMS · EMORY UNIVERSITY · PI PRAHALAD, SAMPATH · 2011 to 2014
$1.5M
NIAMS NIH HHS R01 AR060893NIAMS NIH HHS RC2 AR058934
6 · The paper itself

Abstract

objectiveJuvenile idiopathic arthritis (JIA) affects children of all races. Prior studies suggest that phenotypic features of JIA in African American (AA) children differ from those of non-Hispanic white (NHW) children. We evaluated the phenotypic differences at presentation between AA and NHW children enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry, and replicated the findings in a JIA cohort from a large center in the southeastern United States.

methodsChildren with JIA enrolled in the multicenter CARRA Registry and from Emory University formed the study and replication cohorts. Phenotypic data on non-Hispanic AA children were compared with NHW children with JIA using the chi-square test, Fisher's exact test, and the Wilcoxon signed-rank test.

resultsIn all, 4177 NHW and 292 AA JIA cases from the CARRA Registry and 212 NHW and 71 AA cases from Emory were analyzed. AA subjects more often had rheumatoid factor (RF)-positive polyarthritis in both the CARRA (13.4% vs 4.7%, p = 5.3 × 10(-7)) and the Emory (26.8% vs 6.1%, p = 1.1 × 10(-5)) cohorts. AA children had positive tests for RF and cyclic citrullinated peptide antibodies (CCP) more frequently, but oligoarticular or early onset antinuclear antibody (ANA)-positive JIA less frequently in both cohorts. AA children were older at onset in both cohorts and this difference persisted after excluding RF-positive polyarthritis in the CARRA Registry (median age 8.5 vs 5.0 yrs, p = 1.4 × 10(-8)).

conclusionCompared with NHW children, AA children with JIA are more likely to have RF/CCP-positive polyarthritis, are older at disease onset, and less likely to have oligoarticular or ANA-positive, early-onset JIA, suggesting that the JIA phenotype is different in AA children.

Indexed as

Black or African AmericanArthritis, JuvenileAutoantibodiesChildChild, PreschoolFemaleHumansMalePeptides, CyclicPhenotypeRegistriesRheumatoid FactorSymptom AssessmentAutoantibodiescyclic citrullinated peptidePeptides, CyclicRheumatoid FactorAFRICAN AMERICANJUVENILE IDIOPATHIC ARTHRITISPHENOTYPEREGISTRIES

Identifiers

PMID26879356
PMCPMC4818667
OpenAlexW2323511518

What OpenQuestion holds

Textmetadata
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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.