Evidence map›Paper›PMID 29949836›Full record

ArticleAllergy, asthma & immunology research2018

Association of Genetic Polymorphisms with Atopic Dermatitis, Clinical Severity and Total IgE: A Replication and Extended Study.

Jeong Hyun Kim, So Yeon Lee, Mi Jin Kang, Jisun Yoon, Sungsu Jung, Hyun Ju Cho, Hyo Bin Kim, Soo Jong Hong

Open access · hybridAbstract read
In one paragraph

Article in Allergy, asthma & immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  4. Review
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  7. IDENTIFYING INDIVIDUAL STRESS SUSCEPTIBILITY USING GENOMIC AND IMMUNE BIOMARKERS.Transactions of the American Clinical and Climatological Association · 2019
    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

8 authors at 4 institutions in 1 country.

Jeong Hyun KimDepartment of Medicine, University of Ulsan Collage of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-4879-0075
So Yeon LeeDepartment of Pediatrics, Childhood Asthma Atopy Center, Environmental Health Center, Asan Medical Center, University of Ulsan Collage of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-2499-0702
Mi Jin KangAsan Institute for Life Sciences, University of Ulsan Collage of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-8510-3268
Jisun YoonDepartment of Pediatrics, Childhood Asthma Atopy Center, Environmental Health Center, Asan Medical Center, University of Ulsan Collage of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-4904-9118
Sungsu JungDepartment of Pediatrics, Childhood Asthma Atopy Center, Environmental Health Center, Asan Medical Center, University of Ulsan Collage of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-0559-4982
Hyun Ju ChoDepartment of Pediatrics, Mediplex Sejong Hospital, Incheon, Korea.ORCID https://orcid.org/0000-0003-4282-4000
Hyo Bin KimDepartment of Pediatrics, Inje University Sanggye Paik Hospital, Seoul, Korea.ORCID https://orcid.org/0000-0002-1928-722X
Soo Jong HongDepartment of Pediatrics, Childhood Asthma Atopy Center, Environmental Health Center, Asan Medical Center, University of Ulsan Collage of Medicine, Seoul, Korea. sjhong@amc.seoul.kr.ORCID https://orcid.org/0000-0003-1409-2113
Asan Medical Center · KRInje University Sanggye Paik Hospital · KRSejong General Hospital · KRUlsan College · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAtopic dermatitis (AD) is a common and chronic inflammatory skin disease affecting up to 20% of children and 3% of adults worldwide. Although previous reports including genome-wide association study (GWAS) approaches have identified several risk factors that appear to be associated with AD development, replication studies are lacking. In our current study, we replicated the associations between candidate susceptibility loci and AD.

methodsA total of 885 Korean subjects (425 AD patients and 460 unaffected controls) were genotyped for 17 single nucleotide polymorphisms (SNPs) from previous GWASs and meta-analyses of AD and from immune-related genes.

resultsSeveral SNPs showed significant associations with AD in the case-control analysis (minimum P=0.005 at rs17389644), suggesting that these polymorphisms may be related to this disease. In addition, several SNPs showed significant signals (minimum P=0.004 at rs6473227) in severe AD compared to unaffected controls. In additional linear regression analysis, a few genotypes appeared to have potential effects on the SCORing AD (SCORAD) values (minimum P=0.003 at rs13361382 on TMEM232) and immunoglobulin E (IgE) levels (minimum P<0.0001 at rs4713555 near HLA-DRB1 and HLA-DQA1) in AD patients.

conclusionsOur replication and extended study provide additional supporting information on the genetic associations (especially, variants in TMEM232 and nearby to IL21 and HLA-DRB1/HLA-DQA1) related to AD, its clinical severity and IgE involvement.

Indexed as

Atopic dermatitissingle nucleotide polymorphism, severity

Identifiers

PMID29949836
PMCPMC6021591
OpenAlexW2807882658

What OpenQuestion holds

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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.