Zhang Ximei, Su Dongju, Zhang Xuelong, Sui Hong, Jin Lianhong, Lü Fuzhen, Zhang Jing
Department of Histology and Embryology, Harbin Medical University, Harbin, 150086, China.
Mol Biol Rep. 2009 Jul;36(6):1505-9. doi: 10.1007/s11033-008-9343-z. Epub 2008 Aug 28.
Allergic Rhinitis (AR) and allergic asthma (AS) are very common diseases involving genetic and environmental factors. Most patients with asthma also have rhinitis, which suggests the concept of 'one airway, one disease'. A disintegrin and metalloproteinase 33 (ADAM33) was discovered as the first asthma-susceptible gene by positional cloning. To evaluate the potential influences of ADAM33 gene polymorphisms on concomitant allergic rhinitis and asthma (ARA), a case-control study was conducted in Han population of Northeast China. Six polymorphic sites (V4, T + 1, T2, T1, S1 and Q - 1) were genotyped in 135 ARA patients and 151 controls (CTR). Genotypes were determined by the polymerase chain restriction fragment length polymorphism (PCR-RFLP) method. Data was analyzed using the Chisquaretest and Haploview software. The SNPs (V4 G/C, T2 A/G, T1 G/A, and Q - 1A/G) of the ADAM33 gene may be the causal variants in ARA disease.
变应性鼻炎(AR)和变应性哮喘(AS)是涉及遗传和环境因素的非常常见的疾病。大多数哮喘患者也患有鼻炎,这提示了“一个气道,一种疾病”的概念。通过定位克隆,整合素和金属蛋白酶33(ADAM33)被发现是第一个哮喘易感基因。为了评估ADAM33基因多态性对合并变应性鼻炎和哮喘(ARA)的潜在影响,在中国东北汉族人群中进行了一项病例对照研究。对135例ARA患者和151例对照(CTR)的六个多态性位点(V4、T + 1、T2、T1、S1和Q - 1)进行基因分型。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法确定基因型。使用卡方检验和Haploview软件分析数据。ADAM33基因的单核苷酸多态性(SNPs)(V4 G/C、T2 A/G、T1 G/A和Q - 1A/G)可能是ARA疾病的致病变异。