Laitinen T, Räsänen M, Kaprio J, Koskenvuo M, Laitinen L A
Department of Medicine, Helsinki University Central Hospital, Finland.
Am J Respir Crit Care Med. 1998 Apr;157(4 Pt 1):1073-8. doi: 10.1164/ajrccm.157.4.9704041.
Gene-environment interactions and inheritance of asthma were studied in 16-yr-old twins and their parents who participated in the nationwide Finnish Twin Cohort Study. Between 1991 and 1994, questionnaires, including a question on physician-diagnosed asthma, were mailed to the members of 2,483 twin families. The individual response rate ranged from 82 to 93%. Information on parental asthma status allowed the genetic modeling of asthma data in two different groups of twins. In families where one of the parents was asthmatic, as much as 87% of the variation in susceptibility to asthma in twins was explained by genetic factors. On the other hand, for twins whose parents were unaffected, a model including environmental effect alone was sufficient to explain the development of asthma. Genetic influences could not be totally excluded, but their role was significantly smaller. These results indicate that the presence of asthma in successive generations is more likely caused by shared genes than shared environmental risk factors; however, substantial heterogeneity among families may exist. Genetic analysis, especially among the families with an obvious familial component in development of asthma, may enhance the chances of revealing the pathogenetic mechanisms
在参与全国性芬兰双胞胎队列研究的16岁双胞胎及其父母中,研究了基因 - 环境相互作用与哮喘的遗传情况。1991年至1994年期间,向2483个双胞胎家庭的成员邮寄了问卷,其中包括一个关于医生诊断哮喘的问题。个人回复率在82%至93%之间。关于父母哮喘状况的信息使得能够在两组不同的双胞胎中对哮喘数据进行遗传建模。在父母一方患有哮喘的家庭中,双胞胎对哮喘易感性的变异高达87%可由遗传因素解释。另一方面,对于父母未受影响的双胞胎,仅包含环境效应的模型就足以解释哮喘的发生。遗传影响不能完全排除,但其作用明显较小。这些结果表明,连续几代人中哮喘的出现更可能是由共享基因而非共享环境风险因素引起的;然而,家庭之间可能存在很大的异质性。遗传分析,尤其是在哮喘发病具有明显家族成分的家庭中进行遗传分析,可能会增加揭示发病机制的机会。