García-Sánchez A, Isidoro-García M, García-Solaesa V, Sanz C, Hernández-Hernández L, Padrón-Morales J, Lorente-Toledano F, Dávila I
Departamento de Pediatría, Universidad de Salamanca, Spain; Grupo de Alergia, Instituto Biosanitario de Salamanca (IBSAL), Spain.
Grupo de Alergia, Instituto Biosanitario de Salamanca (IBSAL), Spain; Servicio de Bioquímica Clínica, Complejo Asistencial Universitario de Salamanca, Spain; Departamento de Medicina, Universidad de Salamanca, Spain.
Allergol Immunopathol (Madr). 2015 Nov-Dec;43(6):601-8. doi: 10.1016/j.aller.2014.07.004. Epub 2014 Nov 26.
Asthma is a complex disease determined by the interaction of different genes and environmental factors. The first genetic investigations in asthma were candidate gene association studies and linkage studies. In recent years research has focused on association studies that scan the entire genome without any prior conditioning hypothesis: the so-called genome-wide association studies (GWAS). The first GWAS was published in 2007, and described a new locus associated to asthma in chromosome 17q12-q21, involving the ORMDL3, GSDMB and ZPBP2 genes (a description of the genes named in the manuscript are listed in Table 1). None of these genes would have been selected in a classical genetic association study since it was not known they could be implicated in asthma. To date, a number of GWAS studies in asthma have been made, with the identification of about 1000 candidate genes. Coordination of the different research groups in international consortiums and the application of new technologies such as new generation sequencing will help discover new implicated genes and improve our understanding of the molecular mechanisms underlying the disease.
哮喘是一种由不同基因与环境因素相互作用所决定的复杂疾病。哮喘领域的首批基因研究是候选基因关联研究和连锁研究。近年来,研究聚焦于无需任何先验条件假设即可扫描整个基因组的关联研究,即所谓的全基因组关联研究(GWAS)。首个GWAS于2007年发表,描述了17号染色体q12 - q21上一个与哮喘相关的新基因座,涉及ORMDL3、GSDMB和ZPBP2基因(手稿中提及基因的描述列于表1)。在经典的基因关联研究中,这些基因无一会被选中,因为当时尚不清楚它们与哮喘有关。迄今为止,已开展了多项哮喘GWAS研究,鉴定出约1000个候选基因。国际联盟中不同研究团队的协作以及新一代测序等新技术的应用,将有助于发现新的相关基因,并增进我们对该疾病潜在分子机制的理解。