Evidence map›Paper›PMID 22446962›Full record

ArticleNature genetics2012

A genome-wide association study identifies three new risk loci for Kawasaki disease.

Yoshihiro Onouchi, Kouichi Ozaki, Jane C Burns, Chisato Shimizu, Masaru Terai, Hiromichi Hamada, Takafumi Honda, Hiroyuki Suzuki, Tomohiro Suenaga, Takashi Takeuchi and 35 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Nature genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 176 papers, 11 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
176citing papers in PubMed, 11 pooled it
25.6field-weighted citation impact, top 1% 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

176 citing papers in PubMed, 11 syntheses or guidelines pooled it, 335 citations in OpenAlex.

  1. Intravenous immunoglobulin for the treatment of Kawasaki disease.The Cochrane database of systematic reviews · 2023
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  5. TNF-α blockers for the treatment of Kawasaki disease in children.The Cochrane database of systematic reviews · 2019
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116 more citing papers are in PubMed but not listed here.

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

45 authors at 20 institutions in 2 countries.

Yoshihiro OnouchiLaboratory for Cardiovascular Diseases, Center for Genomic Medicine, RIKEN, Yokohama, Japan. onouchi@src.riken.jp
Kouichi Ozaki
Jane C Burns
Chisato Shimizu
Masaru Terai
Hiromichi Hamada
Takafumi Honda
Hiroyuki Suzuki
Tomohiro Suenaga
Takashi Takeuchi
Norishige Yoshikawa
Yoichi Suzuki
Kumi Yasukawa
Ryota Ebata
Kouji Higashi
Tsutomu Saji
Yasushi Kemmotsu
Shinichi Takatsuki
Kazunobu Ouchi
Fumio Kishi
Tetsushi Yoshikawa
Toshiro Nagai
Kunihiro Hamamoto
Yoshitake Sato
Akihito Honda
Hironobu Kobayashi
Junichi Sato
Shoichi Shibuta
Masakazu Miyawaki
Ko Oishi
Hironobu Yamaga
Noriyuki Aoyagi
Seiji Iwahashi
Ritsuko Miyashita
Yuji Murata
Kumiko Sasago
Atsushi Takahashi
Naoyuki Kamatani
Michiaki Kubo
Tatsuhiko Tsunoda
Akira Hata
Yusuke Nakamura
Toshihiro Tanaka
Japan Kawasaki Disease Genome Consortium
US Kawasaki Disease Genetics Consortium
RIKEN Center for Integrative Medical Sciences · JPChiba University · JPTokyo Women's Medical University · JPWakayama Medical University · JPToho University · JPAsahi Hospital · JPKawasaki Medical School · JPKinan Hospital · JPDokkyo Medical University Saitama Medical Center · JPFujita Health University · JPFunabashi Municipal Medical Center · JPHashimoto Municipal Hospital · JPHidaka Hospital · JPInternational University of Health and Welfare · JPNaga Municipal Hospital · JPOtsu Municipal Hospital · JPRady Children's Hospital-San Diego · USSendai City Hospital · JPSubaru (Japan) · JPThe University of Tokyo · JP

Funding

BASIC STUDIES OF CARDIAC SURGICAL ISCHEMIAF32HL006941 · NHLBI · DUKE UNIVERSITY · PI CHRISTOPHER, THOMAS D · 1985 to 1985
–
NHLBI NIH HHS HL-06941
6 · The paper itself

Abstract

We performed a genome-wide association study (GWAS) of Kawasaki disease in Japanese subjects using data from 428 individuals with Kawasaki disease (cases) and 3,379 controls genotyped at 473,803 SNPs. We validated the association results in two independent replication panels totaling 754 cases and 947 controls. We observed significant associations in the FAM167A-BLK region at 8p22-23 (rs2254546, P = 8.2 × 10(-21)), in the human leukocyte antigen (HLA) region at 6p21.3 (rs2857151, P = 4.6 × 10(-11)) and in the CD40 region at 20q13 (rs4813003, P = 4.8 × 10(-8)). We also replicated the association of a functional SNP of FCGR2A (rs1801274, P = 1.6 × 10(-6)) identified in a recently reported GWAS of Kawasaki disease. Our findings provide new insights into the pathogenesis and pathophysiology of Kawasaki disease.

Indexed as

Genetic LociGenetic MarkersGenome-Wide Association StudyAsian PeopleCase-Control StudiesGenetic Predisposition to DiseaseHumansMucocutaneous Lymph Node SyndromePolymorphism, Single NucleotideReceptors, IgGFCGR2A protein, humanGenetic MarkersReceptors, IgG

Identifiers

PMID22446962
OpenAlexW2015418566

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.