Evidence map›Paper›PMID 24587951›Full record

ArticleAllergy, asthma & immunology research2014

Polymorphisms of ATF6B Are Potentially Associated With FEV1 Decline by Aspirin Provocation in Asthmatics.

Tae-Joon Park, Jeong-Hyun Kim, Charisse F Pasaje, Byung-Lae Park, Joon Seol Bae, Soo-Taek Uh, Yong-Hoon Kim, Mi-Kyeong Kim, Inseon S Choi, Byoung Whui Choi and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Allergy, asthma & immunology research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 10 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

15 authors at 7 institutions in 1 country.

Tae-Joon ParkDepartment of Life Science, Sogang University, Seoul, Korea.
Jeong-Hyun KimDepartment of Life Science, Sogang University, Seoul, Korea.
Charisse F PasajeDepartment of Life Science, Sogang University, Seoul, Korea.
Byung-Lae ParkDepartment of Genetic Epidemiology, SNP Genetics, Inc., Seoul, Korea.
Joon Seol BaeDepartment of Genetic Epidemiology, SNP Genetics, Inc., Seoul, Korea.
Soo-Taek UhGenome Research Center for Allergy and Respiratory Diseases, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.
Yong-Hoon KimDivision of Allergy and Respiratory Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Korea.
Mi-Kyeong KimDepartment of Internal Medicine, Chungbuk National University, College of Medicine, Cheongju, Korea.
Inseon S ChoiDepartment of Allergy, Chonnam National University Medical School and Research Institute of Medical Sciences, Gwangju, Korea.
Byoung Whui ChoiDivision of Pulmonary and Allergy, Department of Internal Medicine, Chung-Ang University Yongsan Hospital, Seoul, Korea.
Hye-Rim ShinGenome Research Center for Allergy and Respiratory Diseases, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.
Jong-Sook ParkGenome Research Center for Allergy and Respiratory Diseases, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.
Insong KohDepartment of Physiology, College of Medicine, Hanyang University, Seoul, Korea.
Choon-Sik ParkGenome Research Center for Allergy and Respiratory Diseases, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.ORCID 0000-0003-2977-0255
Hyoung Doo ShinDepartment of Life Science, Sogang University, Seoul, Korea. ; Department of Genetic Epidemiology, SNP Genetics, Inc., Seoul, Korea.
Sogang University · KRSoonchunhyang University · KRSNP Genetics (South Korea) · KRChonnam National University · KRChung-Ang University Hospital · KRChungbuk National University · KRHanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEndoplasmic reticulum (ER) stress has recently been observed to activate NF-kappaB and induce inflammatory responses such as asthma. Activating transcription factor 6β (ATF6B) is known to regulate ATFα-mediated ER stress response. The aim of this study is to investigate the associations of ATF6B genetic variants with aspirin-exacerbated respiratory disease (AERD) and its major phenotype, % decline of FEV1 by aspirin provocation.

methodsFour common single nucleotide polymorphisms (SNPs) of ATF6B were genotyped and statistically analyzed in 93 AERD patients and 96 aspirin-tolerant asthma (ATA) as controls.

resultsLogistic analysis revealed that 2 SNPs (rs2228628 and rs8111, P=0.008; corrected P=0.03) and 1 haplotype (ATF6B-ht4, P=0.005; corrected P=0.02) were significantly associated with % decline of FEV1 by aspirin provocation, whereas ATF6B polymorphisms and haplotypes were not associated with the risk of AERD.

conclusionsAlthough further functional and replication studies are needed, our preliminary findings suggest that ATF6B may be related to obstructive phenotypes in response to aspirin exposure in adult asthmatics.

Indexed as

aspirin exacerbated respiratory disease (AERD)ATF6Bhaplotypesingle nucleotide polymorphism (SNP)

Identifiers

PMID24587951
PMCPMC3936043
OpenAlexW2099939502

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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.