Evidence map›Paper›PMID 21082224›Full record

ArticleJournal of clinical immunology2011

CTLA-4, position 49 A/G polymorphism associated with coronary artery lesions in Kawasaki disease.

Ho-Chang Kuo, Chi-Di Liang, Hong-Ren Yu, Chih-Lu Wang, I-Chun Lin, Chieh-An Liu, Jen-Chieh Chang, Chiu-Ping Lee, Wei-Chiao Chang, Kuender D Yang

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Article in Journal of clinical immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.0field-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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Association of genetic polymorphisms with osteosarcoma risk: a meta-analysis.International journal of clinical and experimental medicine · 2015
    Review
  3. Article
  4. Article
  5. Article
  6. Understanding the pathogenesis of Kawasaki disease by network and pathway analysis.Computational and mathematical methods in medicine · 2013
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Genetic polymorphisms in Kawasaki disease.Acta pharmacologica Sinica · 2011
    Review
  13. 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 6 institutions in 2 countries.

Ho-Chang KuoDivision of Allergy, Immunology and Rheumatology, Department of Pediatrics, Chang Gung Memorial Hospital-Kaohsiung Medical Center, Kaohsiung, Taiwan.
Chi-Di Liang
Hong-Ren Yu
Chih-Lu Wang
I-Chun Lin
Chieh-An Liu
Jen-Chieh Chang
Chiu-Ping Lee
Wei-Chiao Chang
Kuender D Yang
Kaohsiung Chang Gung Memorial Hospital · TWMemorial Hospital of South Bend · USChang Gung University · TWJen-Ai Hospital · TWKaohsiung Medical University Chung-Ho Memorial Hospital · TWNational Sun Yat-sen University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveKawasaki disease (KD) is a systemic vasculitis of unknown etiology and primarily affects children less than 5 years of age. Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) has been suggested as a candidate gene for conferring susceptibility to autoimmunity. This study examined the correlation of CTLA-4 gene polymorphisms in KD with and without coronary artery lesions (CAL). MATERIALS AND

methodsA total of 233 KD patients and 644 controls were subjected to determination of CTLA-4 polymorphisms at (-318) C/T and (+49) A/G positions by restriction fragment length polymorphism. Susceptibility, CAL, and intravenous immunoglobulin treatment response of KD were then analyzed with genetic variants.

resultsPolymorphisms of CTLA-4 (+49 A/G) and (-318 C/T) were not significantly different between normal children and patients with KD. The CTLA-4 (+49) A allele (AA+AG genotype), however, was significantly associated with CAL formation, especially in female patients.

conclusionsThis study provides the first evidence supporting the association of CTLA-4 (+49) A/G polymorphism with the CAL formation of KD particularly in female patients.

Indexed as

AllelesAntigens, CDChildChild, PreschoolCoronary Artery DiseaseCTLA-4 AntigenFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansInfantMaleMucocutaneous Lymph Node SyndromePolymorphism, Single NucleotideSex FactorsAntigens, CDCTLA-4 AntigenCTLA4 protein, human

Identifiers

PMID21082224
OpenAlexW2060310993

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Registered trials

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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.