Evidence map›Paper›PMID 23167751›Full record

ArticleBMC medical genetics2012

Leukotriene B4 receptor locus gene characterisation and association studies in asthma.

Asif S Tulah, Bianca Beghé, Sheila J Barton, John W Holloway, Ian Sayers

Open access · goldAbstract read
In one paragraph

Article in BMC medical genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 29% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Multi-Omics Analysis IdentifiedInternational journal of molecular sciences · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Development of an AmpliSeqFrontiers in pharmacology · 2018
    Article
  7. Article
  8. Review
  9. Article
  10. Alpha-tryptase gene variation is associated with levels of circulating IgE and lung function in asthma.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2014
    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

5 authors at 5 institutions in 2 countries.

Asif S TulahDivision of Therapeutics and Molecular Medicine, University of Nottingham, Queen's Medical Centre, Nottingham, United Kingdom.
Bianca Beghé
Sheila J Barton
John W Holloway
Ian Sayers
MRC Lifecourse Epidemiology Unit · GBNewcastle University · GBUniversity of Modena and Reggio Emilia · ITUniversity of Nottingham · GBUniversity of Southampton · GB

Funding

Medical Research Council MC_UP_A620_1017
6 · The paper itself

Abstract

backgroundPolymorphisms spanning genes involved in the production of leukotriene B4 (LTB4) e.g. ALOX5AP and LTA4H are associated with asthma susceptibility, suggesting a role for LTB4 in disease. The contribution of LTB4receptor polymorphism is currently unknown. The aim of this study was to characterise the genes for the two pivotal LTB4 receptors, LTB4R1 and LTB4R2 in lung tissue and determine if polymorphisms spanning these genes are associated with asthma and disease severity.

methodsRapid amplification of cDNA ends (RACE) was used to characterise the LTB4R1 and LTB4R2 gene structure in lung. The LTB4R1/2 locus on chromosome 14q11.2 was screened for polymorphic variation. Six LTB4R single nucleotide polymorphisms (SNPs) were genotyped in 370 Caucasian asthma families and 299 Adult Asthma Individuals (n=1877 total) and were evaluated for association with asthma and severity (BTS) outcome measures using Family Based Association Test, linear regression and chi square.

resultsLTB4R1 has complex mRNA arrangement including multiple 5'-untranslated exons, suggesting additional levels of regulation. Three potential promoter regions across the LTB4R1/2 locus were identified with some airway cell specificity. 22 SNPs (MAF>0.01) were validated across the LTB4R locus in the Caucasian population. LTB4R1 and LTB4R2 SNPs were not associated with asthma susceptibility, FEV1 or severity.

conclusionsLTB4R1 and LTB4R2 shows splice variation in the 5'-untranslated region and multiple promoter regions. The functional significance of this is yet to be determined. Both receptor genes were shown to be polymorphic. LTB4R polymorphisms do not appear to be susceptibility markers for the development of asthma in Caucasian subjects.

Indexed as

Polymorphism, Single Nucleotide5' Untranslated RegionsAdolescentAdultAlternative SplicingAsthmaCell Adhesion MoleculesChromosomes, Human, Pair 14ExonsFamilyFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansLeukotriene B4Linear Models5' Untranslated RegionsCell Adhesion MoleculesLeukotriene B4LTB4R2 protein, humanLTB4R protein, humanNerve Tissue ProteinsReceptors, Leukotriene B4Shisa4 protein, rat

Identifiers

PMID23167751
PMCPMC3607986
OpenAlexW2074184697

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.