Green S L, Gaillard M C, Song E, Dewar J B, Halkas A
Department of Medicine, University of the Witwatersrand Medical School, Department of Microbiology, University of the Witwatersrand, Johannesburg, South Africa.
Am J Respir Crit Care Med. 1998 Nov;158(5 Pt 1):1487-92. doi: 10.1164/ajrccm.158.5.9707099.
We used amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) to document the prevalence of three mutations in the beta chain of the high-affinity IgE receptor (Fcepsilon RI-beta): I181L, V183L, and E237G in a sample of black and white asthmatic and control subjects in South Africa to determine whether these variants contribute to the enhanced IgE responses in these groups and also to determine whether the discrepancy in the prevalence of atopy in these groups could be attributed to these variants, as whites tend to be more atopic than blacks. There was a significant difference in the frequency of I181L between white asthmatics (28%) and white control subjects (3%) (p = 0.00001), and between black control subjects (16%) and white control subjects (p = 0.002); no difference in the frequency of I181L was observed between black asthmatics (22%) and black control subjects (16%). V183L was found in one black asthmatic who was also positive for I181L and E237G. There was a significant difference in the frequency of E237G between black asthmatics (20%) and white asthmatics (12%) (p = 0.05), and between control subjects (20%) and white control subjects (5%) (p = 0.003). E237G was more prevalent in blacks (20%) than in whites (8.5%) (p = 0.001). I181L might predispose to atopy in the white population, but not in the black population. The significantly higher prevalence of E237G in blacks than in whites might explain why blacks tend to have more severe asthma than whites and might offer more insight into the higher asthma mortality rate in the black population as compared with the white population.
我们采用扩增阻滞突变系统-聚合酶链反应(ARMS-PCR)来记录南非黑人和白人哮喘患者及对照样本中高亲和力IgE受体(Fcepsilon RI-β)β链上三种突变的流行情况:I181L、V183L和E237G,以确定这些变异是否导致这些群体中IgE反应增强,以及确定这些群体中特应性流行率的差异是否可归因于这些变异,因为白人往往比特应性更明显。白人哮喘患者(28%)和白人对照受试者(3%)之间I181L的频率存在显著差异(p = 0.00001),黑人对照受试者(16%)和白人对照受试者之间也存在显著差异(p = 0.002);在黑人哮喘患者(22%)和黑人对照受试者(16%)之间未观察到I181L频率的差异。在一名同时I181L和E237G呈阳性的黑人哮喘患者中发现了V183L。黑人哮喘患者(20%)和白人哮喘患者(12%)之间E237G的频率存在显著差异(p = 0.05),对照受试者(20%)和白人对照受试者(5%)之间也存在显著差异(p = 0.003)。E237G在黑人(20%)中比在白人(8.5%)中更普遍(p = 0.001)。I181L可能使白人易患特应性,但黑人并非如此。E237G在黑人中的流行率显著高于白人,这可能解释了为什么黑人往往比白人患有更严重的哮喘,并且可能为黑人与白人相比更高的哮喘死亡率提供更多见解。