Genetic markers of children asthma: predisposition to disease course variants.

IF 0.9 Q3 AGRICULTURE, MULTIDISCIPLINARY
M V Smolnikova, Ed W Kasparov, M A Malinchik, K V Kopylova
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引用次数: 0

Abstract

Asthma is a heterogeneous and often difficult to treat condition that results in a disproportionate cost to healthcare systems. Children with severe asthma are at increased risk for adverse outcomes including medication-related side effects, life-threatening exacerbations, and impaired quality of life. An important therapeutic focus is to achieve disease control, which is supposed to involve a personalized approach to treatment of asthma of any severity. Asthma is a multifactorial disease with a significant genetic determinant, however, the inheritance of asthma has not been fully elucidated. Polymorphic genes of inflammatory mediators, including cytokines, play an important role in developing various disease forms. In the current study, large-scale original data on the prevalence of cytokine gene genotypes (IL2, IL4, IL5, IL6, IL10, IL12, IL13, IL17A, IL31, IL33, IFNG, TNFA) among Russian children with asthma in Krasnoyarsk region have been obtained. Genotyping was carried out using real-time PCR. We identified markers predisposing to the development of different variants of the course of childhood asthma: the CT genotype and T allele of IL4 rs2243250 are associated with asthma (p < 0.05), especially in mild asthma and in controlled asthma. The TT genotype and allele T of IL13 rs1800925 are associated with severe and uncontrolled asthma (p < 0.05). The AA genotype of IL17A rs2275913, the TT genotype of IFNG rs2069705 and allelic A variants of TNFA rs1800629 are associated with mild asthma, and the TT genotype of IFNG rs2069705 is additionally associated with controlled asthma. The results obtained will supplement information on the prevalence of polymorphic variants of the cytokine genes in the Russian population and in asthma patients with different disease courses, which is likely to be used in order to shape a plan for Public Health Authority to prevent the development of severe uncontrolled asthma and to optimize personalized therapy.

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儿童哮喘的遗传标记:病程变异的易感性。
哮喘是一种异质性疾病,往往难以治疗,给卫生保健系统带来不成比例的成本。患有严重哮喘的儿童发生不良后果的风险增加,包括药物相关副作用、危及生命的恶化和生活质量受损。一个重要的治疗重点是实现疾病控制,这应该包括个性化的方法来治疗任何严重程度的哮喘。哮喘是一种多因素疾病,具有重要的遗传决定因素,然而,哮喘的遗传尚未完全阐明。包括细胞因子在内的炎症介质的多态性基因在各种疾病的发生中起着重要作用。在目前的研究中,已经获得了俄罗斯克拉斯诺亚尔斯克地区哮喘儿童中细胞因子基因基因型(IL2、IL4、IL5、IL6、IL10、IL12、IL13、IL17A、IL31、IL33、IFNG、TNFA)患病率的大规模原始数据。采用实时荧光定量PCR进行基因分型。我们发现了易诱发儿童哮喘病程不同变异的标志物:il - 4 rs2243250的CT基因型和T等位基因与哮喘相关(p < 0.05),特别是在轻度哮喘和控制哮喘中。IL13 rs1800925的TT基因型和等位基因T与严重哮喘和未控制哮喘相关(p < 0.05)。IL17A rs2275913的AA基因型、IFNG rs2069705的TT基因型和TNFA rs1800629的等位基因A变体与轻度哮喘相关,IFNG rs2069705的TT基因型与控制性哮喘相关。所获得的结果将补充有关俄罗斯人群和不同病程哮喘患者中细胞因子基因多态性变异流行率的信息,这些信息可能用于为公共卫生当局制定计划,以防止发展为严重的不受控制的哮喘并优化个性化治疗。
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来源期刊
Vavilovskii Zhurnal Genetiki i Selektsii
Vavilovskii Zhurnal Genetiki i Selektsii AGRICULTURE, MULTIDISCIPLINARY-
CiteScore
1.90
自引率
0.00%
发文量
119
审稿时长
8 weeks
期刊介绍: The "Vavilov Journal of genetics and breeding" publishes original research and review articles in all key areas of modern plant, animal and human genetics, genomics, bioinformatics and biotechnology. One of the main objectives of the journal is integration of theoretical and applied research in the field of genetics. Special attention is paid to the most topical areas in modern genetics dealing with global concerns such as food security and human health.
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