Evidence map›Paper›PMID 15889128›Full record

ArticleGenes and immunity2005

Family-based association analysis implicates IL-4 in susceptibility to Kawasaki disease.

J C Burns, C Shimizu, H Shike, J W Newburger, R P Sundel, A L Baker, T Matsubara, Y Ishikawa, V A Brophy, S Cheng and 4 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Genes and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 84 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Kawasaki Disease and Allergic Diseases.Frontiers in pediatrics · 2020
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Association between Kawasaki disease and autism: a population-based study in Taiwan.International journal of environmental research and public health · 2014
    Article
  15. Article
  16. Article
  17. Understanding the pathogenesis of Kawasaki disease by network and pathway analysis.Computational and mathematical methods in medicine · 2013
    Review
  18. Article
  19. Elevated Serum Levels of IL-21 in Kawasaki Disease.Allergy, asthma & immunology research · 2012
    Article
  20. Genetic polymorphisms in Kawasaki disease.Acta pharmacologica Sinica · 2011
    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

14 authors at 5 institutions in 2 countries.

J C BurnsDepartment of Pediatrics-0830, University of California San Diego, School of Medicine, La Jolla, CA 92093, USA. jcburns@ucsd.edu
C Shimizu
H Shike
J W Newburger
R P Sundel
A L Baker
T Matsubara
Y Ishikawa
V A Brophy
S Cheng
M A Grow
L L Steiner
N Kono
R M Cantor
GeneTrace Systems (United States) · USBoston Children's Hospital · USUniversity of California, San Diego · USUniversity of California, Los Angeles · USYamaguchi University · JP

Funding

X-LINKED EXTENSION OF THE REVISED HASEMAN-ELSTON ALGORITHM FOR LINKAGE ANALYSISP41RR003655 · NCRR · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1987 to 2011
$11.5M
Genetic Markers and gene expression in Kawasaki DiseaseR01HL069413 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BURNS, JANE C · 2002 to 2010
$5.5M
Matrix Metalloproteinases in Kawasaki DiseaseK24HL074864 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BURNS, JANE C · 2004 to 2008
$526k
NCRR NIH HHS P41 RR003655NCRR NIH HHS RR03655NHLBI NIH HHS K24 HL074864NHLBI NIH HHS K24HL074864NHLBI NIH HHS R01 HL069413NHLBI NIH HHS R01HL69413
6 · The paper itself

Abstract

Several compelling lines of evidence suggest an important influence of genetic variation in susceptibility to Kawasaki disease (KD), an acute vasculitis that causes coronary artery aneurysms in children. We performed a family-based genotyping study to test for association between KD and 58 genes involved in cardiovascular disease and inflammation. By analysis of a cohort of 209 KD trios using the transmission disequilibrium test, we documented the asymmetric transmission of five alleles including the interleukin-4 (IL-4) C(-589)T allele (P=0.03). Asymmetric transmission of the IL-4 C(-589)T was replicated in a second, independent cohort of 60 trios (P=0.05, combined P=0.002). Haplotypes of alleles in IL-4, colony-stimulating factor 2 (CSF2), IL-13, and transcription factor 7 (TCF7), all located in the interleukin gene cluster on 5q31, were also asymmetrically transmitted. The reported associations of KD with atopic dermatitis and allergy, elevated serum IgE levels, eosinophilia, and increased circulating numbers of monocyte/macrophages expressing the low-affinity IgE receptor (FCepsilonR2) may be related to effects of IL-4. Thus, the largest family-based genotyping study of KD patients to date suggests that genetic variation in the IL-4 gene, or regions linked to IL-4, plays an important role in KD pathogenesis and disease susceptibility.

Indexed as

Genetic Predisposition to DiseaseChildChild, PreschoolChromosomes, Human, Pair 5Cohort StudiesCoronary AneurysmDermatitis, AtopicEosinophiliaFamilyFemaleHumansImmunoglobulin EInterleukin-4MacrophagesMaleMucocutaneous Lymph Node SyndromeImmunoglobulin EInterleukin-4Receptors, IgE

Identifiers

PMID15889128
PMCPMC2911125
OpenAlexW1996822812

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.