Krischek B, Tatagiba M
Department of Neurosurgery, University of Tuebingen, Tuebingen, Germany.
Adv Tech Stand Neurosurg. 2008;33:131-47. doi: 10.1007/978-3-211-72283-1_3.
The etiology of intracranial aneurysm formation and rupture remains mostly unknown, but lately several studies have increasingly supported the role of genetic factors. In reports so far, genome-wide linkage studies suggest several susceptibility loci that may contain one or more predisposing genes. Depending on the examined ethnic population, several different non-matching chromosomal regions have been found. Studies of several candidate genes report association with intracranial aneurysms. To date, no single gene has been identified as responsible for intracranial aneurysm formation or rupture. In addition to the well-published environmental factors, such as alcohol intake, hypertension and smoking, only the recent progress in molecular genetics enables us to investigate the possible genetic determinants of this disease. Although a familial predisposition is the strongest risk factor for the development of intracranial aneurysms, the mode of Mendelian inheritance is uncertain in most families. Therefore, multiple genetic susceptibilities in conjunction with the environmental factors are considered to act together in the disease's etiology. Accordingly, researchers performed linkage studies and case-control association studies for the genetic analysis and have identified several genes to be susceptible to intracranial aneurysms. The identification of susceptible genes may lead to the understanding of the mechanism of formation and rupture and possibly lead to the development of a pharmacological therapy. Furthermore, should it be possible to identify a genetic marker associated with an increased risk of formation and rupture of an intracranial aneurysm, the necessity for screening and urgency of treatment could be determined more easily. In this review we summarize the current knowledge of intracranial aneurysm genetics and also discuss the method to detect the causalities. In view of the recent advances made in this field, we also give an outlook on possible future genetically engineered therapies, whose development are well underway.
颅内动脉瘤形成和破裂的病因大多仍不清楚,但最近有几项研究越来越支持遗传因素的作用。在迄今为止的报告中,全基因组连锁研究表明了几个可能包含一个或多个易感基因的易感位点。根据所研究的种族人群,发现了几个不同的、不匹配的染色体区域。对几个候选基因的研究报告了与颅内动脉瘤的关联。迄今为止,尚未确定单一基因是导致颅内动脉瘤形成或破裂的原因。除了已广泛报道的环境因素,如饮酒、高血压和吸烟外,只有分子遗传学的最新进展使我们能够研究这种疾病可能的遗传决定因素。尽管家族易感性是颅内动脉瘤发生的最强危险因素,但在大多数家族中孟德尔遗传模式尚不确定。因此,多种遗传易感性与环境因素被认为在该疾病的病因中共同起作用。相应地,研究人员进行了连锁研究和病例对照关联研究以进行遗传分析,并确定了几个对颅内动脉瘤易感的基因。易感基因的鉴定可能会导致对形成和破裂机制的理解,并可能导致药物治疗的发展。此外,如果能够鉴定出与颅内动脉瘤形成和破裂风险增加相关的遗传标记,那么筛查的必要性和治疗的紧迫性就可以更容易地确定。在这篇综述中,我们总结了颅内动脉瘤遗传学的当前知识,并讨论了检测因果关系的方法。鉴于该领域最近取得的进展,我们还对未来可能的基因工程疗法进行了展望,其开发正在顺利进行。