Evidence map›Paper›PMID 17061022›Full record

ArticleJournal of human genetics2007

ADAM33 polymorphisms are associated with aspirin-intolerant asthma in the Japanese population.

Takuro Sakagami, Nobuyoshi Jinnai, Toshiaki Nakajima, Takashi Sekigawa, Takashi Hasegawa, Eiichi Suzuki, Ituro Inoue, Fumitake Gejyo

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Journal of human genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 41 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

8 authors at 3 institutions in 1 country.

Takuro SakagamiDivision of Respiratory Medicine, Graduate School of Medical and Dental Sciences, Niigata University, 1-757 Asahimachi-dori, Niigata, 951-8510, Japan. takuro@bridge.ocn.ne.jp.
Nobuyoshi JinnaiDivision of Genetic Diagnosis, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Toshiaki NakajimaDivision of Genetic Diagnosis, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Takashi SekigawaDivision of Respiratory Medicine, Graduate School of Medical and Dental Sciences, Niigata University, 1-757 Asahimachi-dori, Niigata, 951-8510, Japan.
Takashi HasegawaNiigata University Medical and Dental Hospital, Niigata, Japan.
Eiichi SuzukiNiigata University Medical and Dental Hospital, Niigata, Japan.
Ituro InoueDivision of Genetic Diagnosis, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Fumitake GejyoDivision of Respiratory Medicine, Graduate School of Medical and Dental Sciences, Niigata University, 1-757 Asahimachi-dori, Niigata, 951-8510, Japan.
Niigata University Medical and Dental Hospital · JPThe University of Tokyo · JPNiigata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple single nucleotide polymorphisms (SNPs) within ADAM33 have been reported to be associated with asthma and bronchial hyper-responsiveness in Caucasian populations. We examined whether these SNPs contribute to a predisposition to asthma, especially aspirin-intolerant asthma (AIA), in the Japanese population. Ten polymorphic sites (ST+4, ST+7, T1, T2, T+1, V-3, V-2, V-1, V4, V5) were genotyped in 102 AIA patients, 282 aspirin-tolerant asthma (ATA) patients and 120 control (CTR) subjects by direct sequencing. Haplotype frequencies were estimated by the expectation-maximization method. Differences in allele and haplotype frequencies among phenotypes were analyzed by the chi-square and permutation tests. ST+7, V-1 and V5 sites in the AIA group were significantly different from those in the ATA group (P=0.034-0.004) and from those in the CTR group (P=0.019-0.002). Haplotypes at three sites (ST+7, V-1, and V5) were significantly different in frequency between the AIA and ATA (P=0.008) or CTR (P=0.001) groups. Sequence variations in ADAM33 are likely to correlate with susceptibility to AIA in the Japanese population.

Indexed as

Polymorphism, Single NucleotideADAM ProteinsAgedAnti-Inflammatory Agents, Non-SteroidalAsian PeopleAspirinAsthmaDrug ToleranceFemaleGene FrequencyGenetic Predisposition to DiseaseHaplotypesHumansJapanLinkage DisequilibriumMaleADAM33 protein, humanADAM ProteinsAnti-Inflammatory Agents, Non-SteroidalAspirin

Identifiers

PMID17061022
OpenAlexW1993700830

What OpenQuestion holds

Textmetadata
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.