Evidence map›Paper›PMID 17672867›Full record

ArticleClinical and experimental immunology2007

Polymorphisms in chemokine receptor genes and susceptibility to Kawasaki disease.

W B Breunis, M H Biezeveld, J Geissler, I M Kuipers, J Lam, J Ottenkamp, A Hutchinson, R Welch, S J Chanock, T W Kuijpers

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% 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, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. The role of infection in Kawasaki syndrome.The Journal of infection · 2013
    Review
  6. Article
  7. Understanding the pathogenesis of Kawasaki disease by network and pathway analysis.Computational and mathematical methods in medicine · 2013
    Review
  8. Article
  9. Abnormal spontaneous interleukin 8 receptor expression: a brief report of two cases.Revista da Sociedade Brasileira de Medicina Tropical · 2012
    Article
  10. Article
  11. Article
  12. 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

10 authors at 5 institutions in 2 countries.

W B BreunisEmma Children's Hospital, Academic Medical Center (AMC), Amsterdam, The Netherlands. w.b.breunis@amc.uva.nl
M H Biezeveld
J Geissler
I M Kuipers
J Lam
J Ottenkamp
A Hutchinson
R Welch
S J Chanock
T W Kuijpers
Academic Medical Center · NLEmma Kinderziekenhuis · NLScience Applications International Corporation (United States) · USNational Institutes of Health · USSanquin · NL

Funding

MOLECULAR STUDY OF HOST RESPONSE/GENETIC RISK FACTORS OF INFECTION COMPLICATIONZ01SC010083 · SC · CLINICAL SCIENCES · PI CHANOCK, STEPHEN J · 1997 to 2007
$1.1M
6 · The paper itself

Abstract

Kawasaki disease (KD) is an acute vasculitis occurring in young children. Its aetiology is unknown, but an infectious agent is assumed. Increased levels of proinflammatory cytokines and chemokines have been reported in KD. Genetic variation in these genes and the receptors for these genes could influence the regulation of cytokines and chemokines. In a case-control study of 170 Dutch Caucasian KD patients and 300 healthy Dutch Caucasian controls, common genetic variants in chemokine receptor genes CCR3, CCR2, CCR5, CX3CR1, CXCR1 and CXCR2 were analysed. Of the eight studied single nucleotide polymorphisms (SNPs) in the CCR3-CCR2-CCR5 gene cluster, four showed a significant association with susceptibility to KD. Moreover the CCR5-Delta32 was observed with an allele frequency of 10.7% in the control population compared to 6.5% in the KD patients (P = 0.04). Two haplotypes of the CCR3-CCR2-CCR5 gene-cluster appear to be at risk haplotypes for KD and one a protective haplotype. No association was observed with the studied SNPs in CX3CR1, CXCR1 and CXCR2. In conclusion, in a Dutch cohort of KD patients an association of KD occurrence with common genetic variants in the chemokine receptor gene-cluster CCR3-CCR2-CCR5 was observed.

Indexed as

Polymorphism, Single NucleotideCase-Control StudiesChromosomes, Human, Pair 3Gene FrequencyGenetic Predisposition to DiseaseHaplotypesHumansMucocutaneous Lymph Node SyndromeReceptors, CCR2Receptors, CCR3Receptors, CCR5Receptors, ChemokineCCR2 protein, humanCCR3 protein, humanReceptors, CCR2Receptors, CCR3Receptors, CCR5Receptors, Chemokine

Identifiers

PMID17672867
PMCPMC2219275
OpenAlexW2170556286

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.