Evidence map›Paper›PMID 34552174›Full record

ArticleScientific reports2021

Expression quantitative trait loci for ETV4 and MEOX1 are associated with adult asthma in Japanese populations.

Yohei Yatagai, Hisayuki Oshima, Tohru Sakamoto, Rie Shigemasa, Haruna Kitazawa, Kentaro Hyodo, Hironori Masuko, Hiroaki Iijima, Takashi Naito, Takefumi Saito and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

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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

13 authors at 4 institutions in 1 country.

Yohei Yatagai *Department of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Hisayuki Oshima *Department of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Tohru Sakamoto *Department of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan. t-saka@md.tsukuba.ac.jp.
Rie ShigemasaDepartment of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Haruna KitazawaDepartment of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Kentaro HyodoDepartment of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Hironori MasukoDepartment of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
Hiroaki IijimaTsukuba Medical Center, Ibaraki, Japan.
Takashi NaitoTsukuba Medical Center, Ibaraki, Japan.
Takefumi SaitoNational Hospital Organization Ibaraki Higashi National Hospital, Ibaraki, Japan.
Tomomitsu HirotaResearch Center for Medical Science, The Jikei University School of Medicine, Tokyo, Japan.
Mayumi TamariResearch Center for Medical Science, The Jikei University School of Medicine, Tokyo, Japan.
Nobuyuki HizawaDepartment of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.
University of Tsukuba · JPJikei University School of Medicine · JPTsukuba Medical Center Hospital · JPNational Hospital Organization · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ETS variant transcription factor 4 (ETV4) is a recently identified transcription factor that regulates gene expression-based biomarkers of asthma and IL6 production in an airway epithelial cell line. Given that ETV4 has not yet been implicated in asthma genetics, we performed genetic association studies of adult asthma in the ETV4 region using two independent Japanese cohorts (a total of 1532 controls and 783 cases). SNPs located between ETV4 and mesenchyme homeobox 1 (MEOX1) were significantly associated with adult asthma, including rs4792901 and rs2880540 (P = 5.63E-5 and 2.77E-5, respectively). The CC haplotype of these two SNPs was also significantly associated with adult asthma (P = 8.43E-7). Even when both SNPs were included in a logistic regression model, the association of either rs4792901 or rs2880540 remained significant (P = 0.013 or 0.007, respectively), suggesting that the two SNPs may have independent effects on the development of asthma. Both SNPs were expression quantitative trait loci, and the asthma risk alleles at both SNPs were correlated with increased levels of ETV4 mRNA expression. In addition, the asthma risk allele at rs4792901 was associated with increased serum IL6 levels (P = 0.041) in 651 healthy adults. Our findings imply that ETV4 is involved in the pathogenesis of asthma, possibly through the heightened production of IL6.

Indexed as

AdultAgedAged, 80 and overAsthmaCase-Control StudiesFemaleGenetic Predisposition to DiseaseHomeodomain ProteinsHumansJapanMaleMiddle AgedPolymorphism, Single NucleotideProto-Oncogene Proteins c-etsQuantitative Trait LociTranscription FactorsETV4 protein, humanHomeodomain ProteinsMEOX1 protein, humanProto-Oncogene Proteins c-etsTranscription Factors

Identifiers

PMID34552174
PMCPMC8458279
OpenAlexW3201004089

What OpenQuestion holds

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LicenceCC BY
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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.