Evidence map›Paper›PMID 26617644›Full record

ReviewKorean circulation journal2015

Consortium-Based Genetic Studies of Kawasaki Disease in Korea: Korean Kawasaki Disease Genetics Consortium.

Jong-Keuk Lee, Young Mi Hong, Gi Young Jang, Sin Weon Yun, Jeong Jin Yu, Kyung Lim Yoon, Kyung-Yil Lee, Hong-Rang Kil, Korean Kawasaki Disease Genetics Consortium

Open access · hybridAbstract readReview
In one paragraph

Review in Korean circulation journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Immunogenetics of Kawasaki disease.Clinical reviews in allergy & immunology · 2020
    Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Establishment of Kawasaki disease database based on metadata standard.Database : the journal of biological databases and curation · 2016
    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

9 authors at 8 institutions in 1 country.

Jong-Keuk LeeAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul, Korea.
Young Mi HongDepartment of Pediatrics, Ewha Womans University Hospital, Seoul, Korea.
Gi Young JangDepartment of Pediatrics, Korea University Hospital, Seoul, Korea.
Sin Weon YunDepartment of Pediatrics, Chung-Ang University Hospital, Seoul, Korea.
Jeong Jin YuDepartment of Pediatrics, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
Kyung Lim YoonDepartment of Pediatrics, Kyung Hee University Hospital at Gangdong, Seoul, Korea.
Kyung-Yil LeeDepartment of Pediatrics, The Catholic University of Korea, Daejeon St. Mary's Hospital, Daejeon, Korea.
Hong-Rang KilDepartment of Pediatrics, Chungnam National University Hospital, Daejeon, Korea.
Korean Kawasaki Disease Genetics Consortium
Asan Medical Center · KRChung-Ang University Hospital · KRChungnam National University Hospital · KREwha Womans University · KRKorea University Medical Center · KRKyung Hee University Hospital at Gangdong · KRThe Catholic University of Korea Daejeon St. Mary's Hospital · KRUniversity of Ulsan · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to perform large-scale genetic studies of Kawasaki disease (KD) in Korea, the Korean Kawasaki Disease Genetics Consortium (KKDGC) was formed in 2008 with 10 hospitals. Since the establishment of KKDGC, there has been a collection of clinical data from a total of 1198 patients, and approximately 5 mL of blood samples per patient (for genomic deoxyribonucleic acid and plasma isolation), using a standard clinical data collection form and a nation-wide networking system for blood sample pick-up. In the clinical risk factor analysis using the collected clinical data of 478 KD patients, it was found that incomplete KD type, intravenous immunoglobulin (IVIG) non-responsiveness, and long febrile days are major risk factors for coronary artery lesions development, whereas low serum albumin concentration is an independent risk factor for IVIG non-responsiveness. In addition, we identified a KD susceptibility locus at 1p31, a coronary artery aneurysm locus (KCNN2 gene), and the causal variant in the C-reactive protein (CRP) promoter region, as determining the increased CRP levels in KD patients, by means of genome-wide association studies. Currently, this consortium is continually collecting more clinical data and genomic samples to identify the clinical and genetic risk factors via a single nucleotide polymorphism chip and exome sequencing, as well as collaborating with several international KD genetics teams. The consortium-based approach for genetic studies of KD in Korea will be a very effective way to understand the unknown etiology and causal mechanism of KD, which may be affected by multiple genes and environmental factors.

Indexed as

Genome-wide association studyMucocutaneous lymph node syndromePolymorphism, single nucleotide

Identifiers

PMID26617644
PMCPMC4661357
OpenAlexW2179845799

What OpenQuestion holds

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LicenceCC BY-NC
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.