Evidence map›Paper›PMID 25295384›Full record

ArticleThe Journal of asthma : official journal of the Association for the Care of Asthma2015

Genetic variation within the histamine pathway among patients with asthma--a pilot study.

Nikita Raje, Carrie A Vyhlidal, Hongying Dai, Bridgette L Jones

Open access · greenAbstract read
In one paragraph

Article in The Journal of asthma : official journal of the Association for the Care of Asthma, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 16 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

4 authors at 2 institutions in 1 country.

Nikita RajeDivision of Allergy/Asthma/Immunology .
Carrie A Vyhlidal
Hongying Dai
Bridgette L Jones
Children's Mercy Hospital · USUniversity of Missouri–Kansas City · US

Funding

Characterization of the Role of Histamine in Children with AsthmaK23HL105783 · NHLBI · CHILDREN'S MERCY HOSP (KANSAS CITY, MO) · PI JONES, BRIDGETTE L. · 2011 to 2015
$641k
NHLBI NIH HHS 1K23HL105783NHLBI NIH HHS K23 HL105783
6 · The paper itself

Abstract

objectiveHistamine is an important mediator in the pathophysiology of asthma. We have previously reported that HRH1 is differentially expressed among those with asthma compared to those without asthma. Single histamine-related genes have also been associated with asthma. We aimed to evaluate known single nucleotide polymorphisms (SNPs) in genes along the histamine biotransformation and response pathway, and determine their association with asthma and HRH1 mRNA expression.

methodsWe enrolled children and adults (n = 93) with/without asthma who met inclusion/exclusion criteria. Genotyping was performed for nine known SNPs in the HDC, HRH1, HRH4, HNMT and ABP1 genes. HRH1 mRNA expression was determined on RNA from buccal tissue. General linear model, Fisher's exact test and Chi-square test were used to determine differences in allele, genotype and haplotype frequency between subjects with and without asthma and differential HRH1 mRNA expression relative to genotype. Statistical significance was determined by p < 0.05.

resultsNo difference was observed in genotype/allele frequency for the nine SNPs between subjects with and without asthma. The HNMT-1639C/-464C/314C/3'UTRA haplotype was more frequently observed in those without asthma than those with asthma (p = 0.03). We also observed genetic differences relative to race and gender. HNMT 314 genotype CT was more frequent in males with asthma compared to those without asthma (p = 0.04).

conclusionsHistamine pathway haplotype was associated with a diagnosis of asthma in our cohort but allele and genotype were not. Subgroup evaluations may also be important. Further studies are needed to determine the potential biological/clinical significance of our findings.

Indexed as

AdultAmine Oxidase (Copper-Containing)AsthmaBlack or African AmericanChildFemaleGene FrequencyGenetic Predisposition to DiseaseGenetic VariationGenotypeHaplotypesHistamineHumansMalePilot ProjectsPolymorphism, Single NucleotideAmine Oxidase (Copper-Containing)AOC1 protein, humanHistamineHRH4 protein, humanReceptors, G-Protein-CoupledReceptors, HistamineReceptors, Histamine H4RNA, MessengerABP1HDCHNMTHRH 1HRH4mRNA expressionsingle nucleotide polymorphisms

Identifiers

PMID25295384
PMCPMC4416071
OpenAlexW2091724605

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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.