Evidence map›Paper›PMID 22105492›Full record

ArticlePediatric cardiology2012

Assessment of risk factors for Korean children with Kawasaki disease.

Jae-Jung Kim, Young Mi Hong, Sin Weon Yun, Myung Ki Han, Kyung-Yil Lee, Min Seob Song, Hyoung-Doo Lee, Dong Soo Kim, Sejung Sohn, Kee-Soo Ha and 6 more

Abstract readComparative StudyMulticenter Study
PubMed Publisher
In one paragraph

Article in Pediatric cardiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
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  7. Article
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  9. Article
  10. Immunogenetics of Kawasaki disease.Clinical reviews in allergy & immunology · 2020
    Review
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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

16 authors at 12 institutions in 2 countries.

Jae-Jung KimAsan Institute for Life Sciences, University of Ulsan College of Medicine, 388-1 Pungnap-2-Dong, Songpa-Gu, Seoul 138-736, Korea.
Young Mi Hong
Sin Weon Yun
Myung Ki Han
Kyung-Yil Lee
Min Seob Song
Hyoung-Doo Lee
Dong Soo Kim
Sejung Sohn
Kee-Soo Ha
Soo-Jong Hong
Kwi-Joo Kim
In-Sook Park
Gi Young Jang
Jong-Keuk Lee
Korean Kawasaki Disease Genetics Consortium
Ulsan College · KRKorea University Medical Center · KRAsan Medical Center · KRCatholic University of Korea · KRChung-Ang University Hospital · KREwha Womans University · KREwha Womans University Medical Center · KRGangneung Asan Hospital · KRInje University Busan Paik Hospital · KRPusan National University Hospital · KRSeverance Hospital · KRUniversity of Ulsan · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kawasaki disease (KD) is the most common cause of acquired heart disease in children. Intravenous immunoglobulin (IVIG) is the standard therapy for KD, but more than 10% of KD patients do not respond to IVIG and are at high risk for the development of coronary artery lesions (CALs). To identify clinical and genetic risk factors associated with CAL development and IVIG nonresponsiveness, this study analyzed the clinical data for 478 Korean KD patients. Multivariate logistic regression analysis showed that incomplete KD, IVIG nonresponse, fever duration of 7 days or longer, and the CC/AC genotypes of the rs7604693 single nucleotide polymorphism (SNP) in the PELI1 gene were significantly associated with the development of CALs, with odds ratios (ORs) ranging from 2.06 to 3.04. The risk of CAL formation was synergistically increased by the addition of individual risk factors, particularly the genetic variant in the PELI1 gene. Multivariate analysis also showed that a serum albumin level of 3.6 g/dl or lower was significantly associated with nonresponsiveness to IVIG [OR, 2.76; 95% confidence interval (CI), 1.34-5.68; P = 0.006]. Conclusively, incomplete KD, IVIG nonresponsiveness, long febrile days, and the rs7604693 genetic variant in the PELI1 gene are major risk factors for the development of CALs, whereas low serum albumin concentration is an independent risk factor for IVIG nonresponsiveness.

Indexed as

Child, PreschoolCoronary VesselsDNAFemaleFollow-Up StudiesGenetic Predisposition to DiseaseGenotypeHumansImmunoglobulins, IntravenousImmunologic FactorsInfantInfant, NewbornInjections, IntravenousMaleMorbidityMucocutaneous Lymph Node SyndromeDNAImmunoglobulins, IntravenousImmunologic FactorsNuclear ProteinsPELI1 protein, humanUbiquitin-Protein Ligases

Identifiers

PMID22105492
OpenAlexW2108133866

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.