Evidence map›Paper›PMID 18629619›Full record

ArticleJournal of clinical immunology2009

The CCR5 (-2135C/T) polymorphism may be associated with the development of Kawasaki disease in Korean children.

Won Kyoung Jhang, Mi-Jin Kang, Hyun-Seung Jin, Jinho Yu, Byoung-ju Kim, Bong Seong Kim, Jong-Keuk Lee, Eul-Ju Seo, Han-Wook Yoo, In Sook Park and 2 more

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In one paragraph

Article in Journal of clinical immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. The role of infection in Kawasaki syndrome.The Journal of infection · 2013
    Review
  5. Understanding the pathogenesis of Kawasaki disease by network and pathway analysis.Computational and mathematical methods in medicine · 2013
    Review
  6. Article
  7. Genetic polymorphisms in Kawasaki disease.Acta pharmacologica Sinica · 2011
    Review
  8. 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

12 authors at 2 institutions in 1 country.

Won Kyoung JhangDepartment of Pediatrics, Asan Medical Center, College of Medicine, Ulsan University, Seoul, South Korea.
Mi-Jin Kang
Hyun-Seung Jin
Jinho Yu
Byoung-ju Kim
Bong Seong Kim
Jong-Keuk Lee
Eul-Ju Seo
Han-Wook Yoo
In Sook Park
Young Mi Hong
Soo-Jong Hong
Asan Medical Center · KREwha Womans University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKawasaki disease (KD) is an acute vasculitis syndrome of unknown etiology that frequently affects small to medium size arteries. C-C chemokine receptor 5 (CCR5) is a chemokine receptor that binds C-C chemokines. This study investigated the association of the CCR5 (-2135C/T) polymorphism with KD in Korean children.

methodsThe study population consisted 189 Korean children with KD and 194 Korean children with congenital heart disease (CHD). CCR5 (-2135C/T) polymorphism genotypes were determined using the single-base extension method.

resultsThe allele frequencies of the CCR5 (-2135C/T) polymorphism differed significantly between CHD children and KD children (-2135T/T, 16.75% vs. 30.05%, aOR 2.14, 95% CI 1.31-3.51). The tested laboratory parameters differed significantly between the KD and CHD groups. The development of coronary artery aneurysm in KD patients was not associated with the CCR5 polymorphism.

conclusionsOur findings suggest that the T allele at the CCR5 (-2135C/T) polymorphism might be associated with the development of KD in Korean children but does not appear to be associated with the development of coronary artery aneurysm.

Indexed as

Genetic Predisposition to DiseaseAllelesChildChild, PreschoolCoronary AneurysmFemaleGene FrequencyGenotypeHumansInfantKoreaMaleMucocutaneous Lymph Node SyndromePolymorphism, Single NucleotideReceptors, CCR5Receptors, CCR5

Identifiers

PMID18629619
OpenAlexW2066442186

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.