Evidence map›Paper›PMID 28886140›Full record

ArticlePloS one2017

Male-specific association of the FCGR2A His167Arg polymorphism with Kawasaki disease.

Young-Chang Kwon, Jae-Jung Kim, Sin Weon Yun, Jeong Jin Yu, Kyung Lim Yoon, Kyung-Yil Lee, Hong-Ryang Kil, Gi Beom Kim, Myung-Ki Han, Min Seob Song and 12 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
4.5field-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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Biomedicines · 2022
    Article
  7. Article
  8. Article
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  10. Review
  11. Rapid review of multisystem inflammatory syndrome in paediatrics: What we know one year later.Canada communicable disease report = Releve des maladies transmissibles au Canada · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Immunogenetics of Kawasaki disease.Clinical reviews in allergy & immunology · 2020
    Review
  17. Review
  18. Article
  19. Article
  20. Antibodies and Immunity During Kawasaki Disease.Frontiers in cardiovascular medicine · 2020
    Review
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

22 authors at 15 institutions in 2 countries.

Young-Chang KwonAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul, Korea.
Jae-Jung KimAsan Institute for Life Sciences, University of Ulsan College of Medicine, 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-Ryang KilDepartment of Pediatrics, Chungnam National University Hospital, Daejeon, Korea.
Gi Beom KimDepartment of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.
Myung-Ki HanDepartment of Pediatrics, University of Ulsan, Gangneung Asan Hospital, Gangneung, Korea.
Min Seob SongDepartment of Pediatrics, Inje University Haeundae Paik Hospital, Busan, Korea.
Hyoung Doo LeeDepartment of Pediatrics, Pusan National University Hospital, Busan, Korea.
Kee-Soo HaDepartment of Pediatrics, Korea University Hospital, Seoul, Korea.
Sejung SohnDepartment of Pediatrics, Ewha Womans University Hospital, Seoul, Korea.
Ryota EbataDepartment of Pediatrics, Chiba-University Graduate School of Medicine, Chiba, Japan.
Hiromichi HamadaDepartment of Pediatrics, Tokyo Women's Medical University Yachiyo Medical Center, Yachiyo, Japan.
Hiroyuki SuzukiDepartment of Pediatrics, Wakayama Medical University, Wakayama, Japan.
Kaoru ItoLaboratory for Cardiovascular diseases, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Yoshihiro OnouchiLaboratory for Cardiovascular diseases, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Young Mi HongDepartment of Pediatrics, Ewha Womans University Hospital, Seoul, Korea.
Gi Young JangDepartment of Pediatrics, Korea University Hospital, Seoul, Korea.
Jong-Keuk LeeAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0003-1125-4017
Korean Kawasaki Disease Genetics Consortium
Ulsan College · KRChiba University · JPEwha Womans University · KRKorea University Medical Center · KRChung-Ang University Hospital · KRChungnam National University Hospital · KRInje University Haeundae Paik Hospital · KRKyung Hee University Hospital at Gangdong · KRPusan National University Hospital · KRRIKEN Center for Integrative Medical Sciences · JPSeoul National University Children's Hospital · KRThe Catholic University of Korea Daejeon St. Mary's Hospital · KRTokyo Women's Medical University · JPUniversity of Ulsan · KRWakayama Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kawasaki disease (KD) is an acute systemic vasculitis that can potentially cause coronary artery aneurysms in some children. KD occurs approximately 1.5 times more frequently in males than in females. To identify sex-specific genetic variants that are involved in KD pathogenesis in children, we performed a sex-stratified genome-wide association study (GWAS), using the Illumina HumanOmni1-Quad BeadChip data (249 cases and 1,000 controls) and a replication study for the 34 sex-specific candidate SNPs in an independent sample set (671 cases and 3,553 controls). Male-specific associations were detected in three common variants: rs1801274 in FCGR2A [odds ratio (OR) = 1.40, P = 9.31 × 10-5], rs12516652 in SEMA6A (OR = 1.87, P = 3.12 × 10-4), and rs5771303 near IL17REL (OR = 1.57, P = 2.53 × 10-5). The male-specific association of FCGR2A, but not SEMA6A and IL17REL, was also replicated in a Japanese population (OR = 1.74, P = 1.04 × 10-4 in males vs. OR = 1.22, P = 0.191 in females). In a meta-analysis with 1,461 cases and 5,302 controls, a very strong association of KD with the nonsynonymous SNP rs1801274 (p.His167Arg, previously assigned as p.His131Arg) in FCGR2A was confirmed in males (OR = 1.48, P = 1.43 × 10-7), but not in the females (OR = 1.17, P = 0.055). The present study demonstrates that p.His167Arg, a KD-associated FCGR2A variant, acts as a susceptibility gene in males only. Overall, the gender differences associated with FCGR2A in KD provide a new insight into KD susceptibility.

Indexed as

Amino Acid SubstitutionCodonGenetic Predisposition to DiseasePolymorphism, Single NucleotideAllelesAsian PeopleCase-Control StudiesFemaleGenetic Association StudiesGenotypeHumansJapanMaleMucocutaneous Lymph Node SyndromeOdds RatioReceptors, IgGCodonFCGR2A protein, humanIL17REL protein, humanReceptors, IgGReceptors, Interleukin-17SEMA6A protein, humanSemaphorins

Identifiers

PMID28886140
PMCPMC5590908
OpenAlexW2751813659

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.