Zeinaly Ilghar, Vossoughi Naghmeh, Elieh Ali Komi Daniel, Kazemi Tohid, Babaloo Zohreh, Razavi Alireza, Sajay-Asbaghi Mohammad, Sadeghi-Shabestari Mahnaz
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran AND Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Iran J Allergy Asthma Immunol. 2018 Dec 1;17(6):526-532.
Orosomucoid 1-like 3 (ORMDL3) gene, located on chromosome 17q21, is an asthma candidate gene that encodes ORMDL3. This molecule has been reported to play a role in airway remodeling and bronchial hyper-responsiveness. In this study, we aimed to investigate the possible association of ORMDL3 single nucleotide polymorphism (SNP) (rs12603332) with susceptibility to allergic asthma in Iranian Northwestern Azeri population. 193 asthmatic patients and 185 normal individuals were included. Genomic DNA was extracted and genotyping was performed by standard restriction fragment length polymorphism-polymerase chain reaction RFLP-PCR method using BstUI restriction enzyme. Our results showed dominant presence of TC genotype and C allele in both patients (49.2% and 59.8%, respectively) and controls (48.6% and 60%, respectively). Frequency of genotypes and alleles showed no significant difference between two groups (p=0.994 and p=1.00, respectively). None of alleles could be defined as risk allele for allergic asthma (OR=0.99, 0.88-1.12, 95% CI). We failed to show significant association between ORMDL3 rs12603332 with predisposition to allergic asthma in Iranian Northwestern Azeri population. More studies with larger number of participants should be done to find more reliable results for such association.
类正五聚蛋白1样3(ORMDL3)基因位于17号染色体q21区,是一个哮喘候选基因,编码ORMDL3。据报道,该分子在气道重塑和支气管高反应性中发挥作用。在本研究中,我们旨在调查伊朗西北部阿塞拜疆人群中ORMDL3单核苷酸多态性(SNP)(rs12603332)与过敏性哮喘易感性之间的可能关联。纳入了193例哮喘患者和185名正常个体。提取基因组DNA,并使用BstUI限制性内切酶通过标准限制性片段长度多态性-聚合酶链反应(RFLP-PCR)方法进行基因分型。我们的结果显示,患者组(分别为49.2%和59.8%)和对照组(分别为48.6%和60%)中TC基因型和C等位基因均占主导地位。两组之间基因型和等位基因频率无显著差异(分别为p = 0.994和p = 1.00)。没有一个等位基因可被定义为过敏性哮喘的风险等位基因(OR = 0.99,0.88 - 1.12,95%CI)。我们未能显示出伊朗西北部阿塞拜疆人群中ORMDL3 rs12603332与过敏性哮喘易感性之间存在显著关联。应该进行更多参与者数量更多的研究,以获得关于这种关联的更可靠结果。