MMP9 Q279R基因多态性儿童的过敏风险及其免疫表型

Q3 Medicine
K. Starkova, O. Dolgikh, T.A. Legostaeva, V. Ukhabov
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引用次数: 3

摘要

科学研究的重点是过敏性疾病依赖于最新的分子遗传学方法来识别个体遗传变异性;这似乎是实施旨在早期发现和减轻此类疾病风险的规划的重要阶段。在这项研究中,我们的目的是确定过敏性疾病儿童Q279R MMP9基因多态性(rs17576)和生物培养基中苯污染相关的免疫调节特征。试验组包括33名患有过敏性疾病的儿童;参照组由40名相对健康的儿童组成。流式细胞术鉴定cd标记物。采用实时聚合酶链反应进行基因分型。研究显示,在生物培养基中苯污染升高的情况下,过敏性疾病患儿的总IgE、IL-4和TNFalfa水平升高,是对照组的1.2-4.2倍(χ = 0.006-0.03)。Q279R MMP9基因多态性在试验组儿童中GG和AG基因型的真实发生率更高,比对照组高1.7倍。这允许考虑MMP9基因的等位基因G作为过敏性疾病儿童的敏感性标记(OR = 2.34;95% ci = 1.17-4.65)。我们发现,在被检查的变应性疾病儿童中,等位基因G携带者的总IgE水平比纯合子AA基因型携带者高2.8倍,IL-4和TNFalfa的表达比纯合子AA基因型携带者高1.4倍和1.3倍(χ = 0.020-0.042)。Logistic回归分析证实了优势模型的充分性(p = 0.01),表明携带Q279R MMP9基因多态性的AG和GG基因型与发生过敏可能存在关联(OR = 3.61;95% ci = 1.34-9.71)。G等位基因携带者与AA基因型携带者相比,发生生物介质苯污染和基质金属蛋白酶MMP9 (rs17576)基因多态性的过敏风险高2.1倍(RR = 2.08;95% ci = 1.13-3.83)。这允许考虑将MMP9 Q279R基因的等位基因G作为过敏性疾病儿童的敏感性标记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of allergy and its immune phenotypes in children with MMP9 Q279R gene polymorphism
Scientific research with its focus on allergic diseases relies on up-to-date molecular-genetic methods for identifying individual genetic variability; it seems an important stage in the implementation of programs with their aim to early detect and mitigate risks of such diseases. In this study, our aim was to identify features of immune regulation associated with Q279R MMP9 gene polymorphism (rs17576) and benzene contamination in biological media in children with allergic diseases. The test group included 33 children with allergic diseases; the reference group consisted of 40 relatively healthy children. CD-markers were identified with flow cytometry. Genotyping was performed with a real-time polymerase chain reaction. The research revealed elevated levels of total IgE, IL-4 and TNFalfa under elevated benzene contamination in biological media that were by 1.2–4.2 times higher in the examined children with allergic diseases than in the reference group (р = 0.006–0.03). Q279R MMP9 gene polymorphismin in children from the test group had authentically more frequent oc-currence of the GG and AG genotypes, by 1.7 times higher than in the reference group. This allows considering the allele G of the MMP9 gene as a sensitivity marker in children with allergic diseases (OR = 2.34; 95 % CI = 1.17–4.65). We established a growth by 2.8 times in total IgE level and greater IL-4 and TNFalfa expression, by 1.4 and 1.3 times accordingly, in carriers of the allele G against those carrying the homozygote AA genotype among the examined children with allergic diseases (р = 0.020–0.042). Logistic regression analysis established the adequacy of the dominant model (p = 0.01) and revealed a possible association between carriage of the AG and GG genotypes of Q279R MMP9 gene polymorphism and developing allergy (OR = 3.61; 95 % CI = 1.34–9.71). A risk of developing allergy combined with benzene contamination in biological media and gene polymorphism of matrix metalloproteinase MMP9 (rs17576) is by 2.1 times higher for the allele G carriers against the AA genotype carriers (RR = 2.08; 95 % CI = 1.13–3.83). This allows considering the allele G of the MMP9 Q279R gene as a sensitivity marker in children with allergic diseases.
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来源期刊
Health Risk Analysis
Health Risk Analysis Medicine-Health Policy
CiteScore
1.30
自引率
0.00%
发文量
38
审稿时长
20 weeks
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