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颈动脉夹层危险因素研究中的遗传学方法。

Genetic approaches in the study of risk factors for cervical artery dissection.

作者信息

Grond-Ginsbach G, Debette S, Pezzini A

机构信息

Neurologische Klinik der Universität Heidelberg, Heidelberg, Deutschland.

出版信息

Front Neurol Neurosci. 2005;20:30-43. doi: 10.1159/000088133.

Abstract

The familial risk of spontaneous cervical artery dissections (sCAD) and the prevalence of the disease in the general population are not well known, making it difficult to estimate the importance of genetic risk factors in sCAD. sCAD is associated in rare cases with inherited diseases such as Ehlers-Danlos syndrome or osteogenesis imperfecta. In most instances, however, sCAD occurs in the absence of known heritable diseases. Genetic risk factors might play a role in further associated conditions, like the ultrastructural connective tissue alterations that are found in skin biopsies of most patients. Systematic mutation search in genes known for their implication in connective tissue disorders has been disappointing apart from rare missense mutations in the genes encoding type V collagen that were found in a minority of patients with sCAD. Efforts are now focusing on genetic linkage studies scanning the whole genome for markers that cosegregate with the above-mentioned dermal connective tissue alterations. Concomitantly, genetic association studies tested the association between sCAD and candidate genes that were selected a priori on pathophysiological arguments, in particular genes playing a role in the extracellular matrix, endothelial function, or inflammatory processes. Most association studies reported until now were negative, apart from one showing an association with a polymorphism in the MTHFR gene and another with a polymorphism in the ICAM-1 gene. However, the results of the association studies published so far must be interpreted cautiously because of the small sample sizes.

摘要

自发性颈内动脉夹层(sCAD)的家族风险以及该疾病在普通人群中的患病率尚不清楚,因此难以评估遗传风险因素在sCAD中的重要性。在罕见情况下,sCAD与遗传性疾病相关,如埃勒斯-当洛综合征或成骨不全症。然而,在大多数情况下,sCAD是在没有已知遗传性疾病的情况下发生的。遗传风险因素可能在进一步的相关病症中起作用,例如在大多数患者的皮肤活检中发现的超微结构结缔组织改变。除了在少数sCAD患者中发现的编码V型胶原的基因中罕见的错义突变外,对已知与结缔组织疾病有关的基因进行系统的突变搜索一直令人失望。目前的努力集中在遗传连锁研究上,扫描整个基因组以寻找与上述皮肤结缔组织改变共分离的标记。与此同时,遗传关联研究测试了sCAD与基于病理生理学论据预先选择的候选基因之间的关联,特别是在细胞外基质、内皮功能或炎症过程中起作用的基因。到目前为止报道的大多数关联研究都是阴性的,只有一项研究显示与MTHFR基因的多态性有关,另一项研究显示与ICAM-1基因的多态性有关。然而,由于样本量小,迄今为止发表的关联研究结果必须谨慎解释。

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