Association of AQP5 gene polymorphisms with osmotic airway hyperresponsiveness in asthma

IF 2.7 4区 医学 Q2 GENETICS & HEREDITY
D. Naumov, O. Kotova, D. Gassan, E. Afanas'eva, J. Perelman, V. Kolosov
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引用次数: 0

Abstract

Background: Airway hyperresponsiveness (AHR) to osmotic stimuli is common and clinically relevant in asthma. AQP5 is a membrane water channel that may be functionally implicated in airway inflammation and hypersecretion. Objectives: The aim was to assess the effect of AQP5 SNPs on osmotic AHR in asthma patients. Methods: The study enrolled 274 patients with mild-to-moderate asthma, mean age 36.2±0.67 years. The patients underwent bronchoprovocation with 3-min inhalation of distilled water (hypoosmotic stimulus) and hypertonic saline aerosol (hyperosmotic stimulus). Lung function was measured by spirometry before and after each challenge. AQP5 SNPs (rs3759129, rs3736309, rs296756, rs1964676) were genotyped by LATE-PCR. Results: Association with hypoosmotic AHR was found for rs3759129 and rs296756. C allele of rs3759129 was protective against hypoosmotic AHR as AC heterozygotes had less profound response to the challenge compared to AA carriers (ΔFEV1 -1.4 (-6.3; 2.33)% vs. -5.4 (-12.0; -1.0)%, p=0.001; ΔFEF25-75 -1.0 (-18.0; 14.0)% vs. -9.1 (-21.1; 1.2)%, p=0.009). G allele of rs296756 in homozygous state also had protective effect. AA and AG (but not GG) carriers showed marked reduction in airway patency (ΔFEV1 -5,5 (-12,0; -0,8)% vs. -0,2 (-4,5; 3,4)%, p=0.004; ΔFEF25-75 -9,6 (-22,0; 2,3)% vs. 2,0 (-8,9; 9,0)%, p=0.008, for AA and GG genotypes, respectively). rs3759129 also influenced hyperosmotic AHR: all patients with the AHR had AA genotype while 27% of patients without the AHR had AC genotype (p=0.006). Conclusions:AC genotype of rs3759129 and GG genotype of rs296756 exert a protective effect on hypoosmotic AHR. AC genotype of rs3759129 also protects asthma patients from hyperosmotic AHR.
AQP5基因多态性与哮喘患者渗透性气道高反应性的关系
背景:气道对渗透刺激的高反应性(AHR)在哮喘中很常见,并且与临床相关。AQP5是一种膜水通道,在功能上可能与气道炎症和高分泌有关。目的:评估AQP5 SNPs对哮喘患者渗透性AHR的影响。方法:本研究纳入274例轻中度哮喘患者,平均年龄36.2±0.67岁。患者通过吸入蒸馏水(低渗透刺激)和高渗盐水气雾剂(高渗刺激)3分钟进行支气管激发。在每次激发前后通过肺活量测定法测量肺功能。AQP5 SNPs(rs3759129,rs3736309,rs296756,rs1964676)通过LATE-PCR进行基因分型。结果:rs3759129和rs296756与低渗透AHR相关。rs3759129的C等位基因对低渗透性AHR具有保护作用,因为与AA携带者相比,AC杂合子对攻击的反应不那么深刻(ΔFEV1-1.4(-6.3;2.33)%对-5.4(-12.0;-1.0)%,p=0.001;ΔFEF25-75-1.0(-18.0;14.0)%对-9.1(-21.1;1.2)%,p=0.009)。rs296756的G等位基因在纯合状态下也具有保护作用。AA和AG(但不是GG)携带者的气道通畅性显著降低(ΔFEV1-5,5(-12,0;-0,8)%对-0,2(-4,5;3,4)%,p=0.004;AA和GG基因型的ΔFEF25-75-9,6(-22,0;2,3)%对2,0(-8,9;9,0)%,p=0.008)。rs3759129也影响高渗性AHR:所有AHR患者均具有AA基因型,27%的无AHR患者具有AC基因型(p=0.006)。rs3759129的AC基因型也保护哮喘患者免受高渗性AHR的影响。
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来源期刊
Genes and Environment
Genes and Environment Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
4.00
自引率
0.00%
发文量
24
审稿时长
27 weeks
期刊介绍: Genes and Environment is an open access, peer-reviewed journal that aims to accelerate communications among global scientists working in the field of genes and environment. The journal publishes articles across a broad range of topics including environmental mutagenesis and carcinogenesis, environmental genomics and epigenetics, molecular epidemiology, genetic toxicology and regulatory sciences. Topics published in the journal include, but are not limited to, mutagenesis and anti-mutagenesis in bacteria; genotoxicity in mammalian somatic cells; genotoxicity in germ cells; replication and repair; DNA damage; metabolic activation and inactivation; water and air pollution; ROS, NO and photoactivation; pharmaceuticals and anticancer agents; radiation; endocrine disrupters; indirect mutagenesis; threshold; new techniques for environmental mutagenesis studies; DNA methylation (enzymatic); structure activity relationship; chemoprevention of cancer; regulatory science. Genetic toxicology including risk evaluation for human health, validation studies on testing methods and subjects of guidelines for regulation of chemicals are also within its scope.
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