Evidence map›Paper›PMID 29969634›Full record

ArticleThe Journal of allergy and clinical immunology2018

Genetic variants with gene regulatory effects are associated with diisocyanate-induced asthma.

David I Bernstein, Zana L Lummus, Banu Kesavalu, Jianbo Yao, Leah Kottyan, Daniel Miller, André Cartier, Maria-Jesús Cruz, Catherine Lemiere, Xavier Muñoz and 6 more

Abstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
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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

16 authors at 8 institutions in 3 countries.

David I BernsteinDivision of Immunology, Allergy and Rheumatology, University of Cincinnati College of Medicine, Cincinnati, Ohio. Electronic address: bernstdd@ucmail.uc.edu.
Zana L LummusDivision of Immunology, Allergy and Rheumatology, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Banu KesavaluDivision of Immunology, Allergy and Rheumatology, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Jianbo YaoDivision of Animal and Nutritional Sciences, West Virginia University, Morgantown, WV.
Leah KottyanCenter for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Daniel MillerCenter for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
André CartierDepartment of Medicine, Université de Montréal, and Respiratory Division, Hôpital du Sacré-Coeur de Montréal, Montreal, Quebec, Canada.
Maria-Jesús CruzRespiratory Department, Hospital Vall D'Hebron, Barcelona and CIBER de Enfermedades Respiratorias CIBERES, Madrid, Spain.
Catherine LemiereDepartment of Medicine, Université de Montréal, and Respiratory Division, Hôpital du Sacré-Coeur de Montréal, Montreal, Quebec, Canada.
Xavier MuñozRespiratory Department, Hospital Vall D'Hebron, Barcelona and CIBER de Enfermedades Respiratorias CIBERES, Madrid, Spain.
Santiago QuirceDepartment of Allergy, Hospital La Paz-IdiPAZ and CIBER de Enfermedades Respiratorias CIBERES, Madrid, Spain.
Susan TarloDepartment of Medicine, University of Toronto, Toronto, Ontario, Canada.
Joaquin SastreDepartment of Allergy, Fundación Jiménez Díaz and CIBER de Enfermedades Respiratorias CIBERES, Madrid, Spain.
Louis Philippe BouletInstitut Universitaire de Cardiology et de Pneumologie de Quebec, Université Laval, Hôpital Laval, Sainte-Foy, Quebec, Canada.
Matthew T WeirauchCenter for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio; Divisions of Biomedical Informatics and Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Kenneth KaufmanCenter for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio; Cincinnati VA Medical Center, Cincinnati, Ohio.
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESCincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · USHôpital du Sacré-Cœur de Montréal · CACincinnati VA Medical Center · USUniversité Laval · CAUniversity of Toronto · CAWest Virginia University · US

Funding

Tissue Repository CoreP30AR070549 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI Grant Sanford Schulert · 2016 to 2026
$7.7M
Effect of disease-associated genetic variants on viral protein DNA bindingR21HG008186 · NHGRI · CINCINNATI CHILDRENS HOSP MED CTR · PI WEIRAUCH, MATTHEW TYSON · 2015 to 2017
$464k
Enhanced proteomics capabilities for quantitation of proteins with a triple quadS10RR027015 · NCRR · UNIVERSITY OF CINCINNATI · PI GREIS, KENNETH DONALD · 2010 to 2010
$426k
NCRR NIH HHS S10 RR027015NHGRI NIH HHS R21 HG008186NIAMS NIH HHS P30 AR070549NIOSH CDC HHS R01 OH008795
6 · The paper itself

Abstract

backgroundIsocyanates are major causes of occupational asthma, but susceptibility and mechanisms of diisocyanate-induced asthma (DA) remain uncertain.

objectiveThe aim of this study was to identify DA-associated functional genetic variants through next-generation sequencing (NGS), bioinformatics, and functional assays.

methodsNGS was performed in 91 workers with DA. Fourteen loci with known DA-associated single nucleotide polymorphisms (SNPs) were sequenced and compared with data from 238 unexposed subjects. Ranking of DA-associated SNPs based on their likelihood to affect gene regulatory mechanisms in the lung yielded 21 prioritized SNPs. Risk and nonrisk oligonucleotides were tested for binding of nuclear extracts from A549, BEAS-2B, and IMR-90 lung cell lines by using electrophoretic mobility shift assays. DNA constructs were cloned into a pGL3 promoter vector for luciferase gene reporter assays.

resultsNGS detected 130 risk variants associated with DA (3.1 × 10

conclusionsWe identified 5 DA-associated potential regulatory SNPs. Four variants exhibited effects on gene regulation (ATF rs11571537, CDH17 rs2446824 and rs2513789, and TACR1 rs2287231). A fifth variant (FAM71A rs147978008) showed nonrisk allele preferential binding to H1 histones. These results demonstrate that many DA-associated genetic variants likely act by modulating gene regulation.

Indexed as

Activating Transcription Factor 3AdultAir Pollutants, OccupationalAsthma, OccupationalCadherinsCarrier ProteinsCell LineFemaleGenetic Predisposition to DiseaseHumansIsocyanatesMaleMiddle AgedPolymorphism, Single NucleotideReceptors, Neurokinin-1Young AdultActivating Transcription Factor 3Air Pollutants, OccupationalATF3 protein, humanCadherinsCarrier ProteinsCDH17 protein, humanGARIN4 protein, humanIsocyanatesReceptors, Neurokinin-1TACR1 protein, humanAsthmabioinformaticsdiisocyanateelectrophoretic mobility shift assayfunctional genomicsgene regulationgenetichistoneisocyanateluciferase assaynext-generation sequencingoccupational asthmaoligonucleotidesingle nucleotide polymorphism

Identifiers

PMID29969634
PMCPMC13051369
OpenAlexW2809846589

What OpenQuestion holds

Textmetadata
LicenceTDM
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.