Dar Aamna, Faryal Rani, Masood Nosheen
Department of Microbiology, Quaid e Azam University, Islamabad, Pakistan.
Department of Environmental Sciences/Biotechnology, Fatima Jinnah Women University, Rawalpindi, Pakistan.
Genes Dis. 2017 Jan 17;4(2):111-115. doi: 10.1016/j.gendis.2017.01.001. eCollection 2017 Jun.
Allergic asthma is a diverse chronic respiratory disease characterized by the inflammation of the lower airway disease affecting many people around the world with rising morbidity and mortality. Association between asthma and certain demographic features was studied in relation to genotype from 244 allergic individuals of local population. Skin prick test was used to confirm asthma. Genetic polymorphism in Glutathione-S-transferases (GSTs) was studied using multiplex PCR based method and IgE level by ELISA. Pollen and dust were the major causative aeroallergens (26%), which were associated to higher IgE levels ( < 0.05). Smoking was found to be significantly associated with asthma in only males ( = 0.004). A low prevalence of null genotype of both GSTM1 and GSTT1 genes was observed in the patients (4.34%) compared to control group (14%). No association of combined GSTM1 and GSTT1 null genotype was found with the asthma in local population. GSTM1+ and GSTT- genotype had higher risk (OR = 1.3681, = 0.001) for development of asthma. There was a significant association of asthma with combined genotype of GSTM1+ and GSTT- when data was analyzed on gender basis in males ( = 0.006) and highly significant in age range of 26-40 years ( = 0.001). Combined GSTM and GSTT genotype was found to be risk factor for asthma in addition to family history in male patients. However a data with large patient size and different ethnic distribution may reveal the exact etiology.
过敏性哮喘是一种多样的慢性呼吸道疾病,其特征为下呼吸道炎症,影响着世界各地众多人群,发病率和死亡率不断上升。我们针对当地人群中244名过敏个体,研究了哮喘与某些人口统计学特征之间的关联,并将其与基因型相关联。采用皮肤点刺试验来确诊哮喘。使用基于多重PCR的方法研究谷胱甘肽 - S - 转移酶(GSTs)的基因多态性,并通过酶联免疫吸附测定法检测IgE水平。花粉和灰尘是主要的气源性过敏原(26%),与较高的IgE水平相关(P < 0.05)。仅在男性中发现吸烟与哮喘显著相关(P = 0.004)。与对照组(14%)相比,患者中GSTM1和GSTT1基因纯合缺失基因型的患病率较低(4.34%)。在当地人群中,未发现GSTM1和GSTT1基因纯合缺失基因型组合与哮喘之间存在关联。GSTM1 +和GSTT -基因型患哮喘的风险较高(OR = 1.3681,P = 0.001)。当按性别分析数据时,GSTM1 +和GSTT -基因型组合与男性哮喘显著相关(P = 0.006),在26 - 40岁年龄组中高度显著(P = 0.001)。除家族史外,GSTM和GSTT基因型组合被发现是男性患者患哮喘的危险因素。然而,如果有更大样本量且不同种族分布的数据,可能会揭示确切的病因。