Association of the 5HTR2C gene Ser23 variation with childhood allergic asthma

IF 1.2 Q3 MULTIDISCIPLINARY SCIENCES The EuroBiotech Journal Pub Date : 2020-05-28 DOI:10.22541/au.159064938.87006424
S. Temel, M. C. Ergoren, Izel Yilmaz, Ozel Yuruker, H. Çobanogullari, O. Tosun, H. Oral, N. Bahçeci̇ler
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Abstract

Abstract Objective: Allergic asthma is the most frequently observed subtype of individuals with asthma. The effects of serotonin plays in the pathophysiology of asthma has not been clearly determined. Thus, this study aimed to investigate the association between the 5HTR2C gene rs 6318 G>C polymorphism and allergic asthma in pediatric patients in Cyprus. Methods: This study included total number of 177 individuals with 118 control and 59 pediatric patients (43 atopic and 16 non-atopic asthma patient). A skin prick test was performed for each patient to confirm asthma diagnosis and to evaluate atopic status. Genotyping for the 5HTR2C was completed by Real Time-PCR analysis. Results: The genotype distribution frequencies were not in agreement with the Hardy-Weinberg Equilibrium in the patients’ group (p<0.00001). The frequency of the risk allele (allele C) was not significantly different between the patient and control groups (p=0.255). The genotypic distribution between atopic asthma and non-atopic asthma within the patientsts groups was not in agreement with the Hardy-Weinberg Equilibrium (p=0.006). However, risk allele presence showed a statistically significant association with atopy-related asthma (p=0.037). Discussion & Conclusion: Overall, despite the finding of no association between the 5HTR2C rs6318 C allele and childhood asthma, the current results indicated that there is a strong association between the 5HTR2C rs6318 C variant and childhood atopic asthma.
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5HTR2C基因Ser23变异与儿童过敏性哮喘的关系
摘要目的:变应性哮喘是哮喘患者中最常见的亚型。血清素在哮喘病理生理中的作用尚未明确。因此,本研究旨在探讨塞浦路斯儿童5HTR2C基因rs 6318 G>C多态性与过敏性哮喘的关系。方法:本研究共纳入177例患者,其中对照组118例,儿科患者59例(43例特应性哮喘,16例非特应性哮喘)。对每位患者进行皮肤点刺试验以确认哮喘诊断并评估特应性状态。采用Real - Time-PCR分析完成5HTR2C基因分型。结果:患者组基因型分布频率不符合Hardy-Weinberg平衡(p<0.00001)。风险等位基因(等位基因C)的频率在患者和对照组之间无显著差异(p=0.255)。患者组内特应性哮喘与非特应性哮喘的基因型分布不符合Hardy-Weinberg平衡(p=0.006)。然而,风险等位基因的存在与特异型相关性哮喘有统计学意义(p=0.037)。讨论与结论:总体而言,尽管没有发现5HTR2C rs6318 C等位基因与儿童哮喘之间的关联,但目前的结果表明5HTR2C rs6318 C变异与儿童特应性哮喘之间存在很强的关联。
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来源期刊
The EuroBiotech Journal
The EuroBiotech Journal Agricultural and Biological Sciences-Food Science
CiteScore
3.60
自引率
0.00%
发文量
17
审稿时长
10 weeks
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