Revencu N, Vikkula M
Laboratory of Human Molecular Genetics, Christian de Duve Institute of Cellular Pathology, Université catholique de Louvain, Avenue Hippocrate 74, BP 75.39, B-1200 Brussels, Belgium.
J Med Genet. 2006 Sep;43(9):716-21. doi: 10.1136/jmg.2006.041079. Epub 2006 Mar 29.
Cerebral cavernous malformation (CCM) is a vascular malformation causing neurological problems, such as headaches, seizures, focal neurological deficits, and cerebral haemorrhages. CCMs can occur sporadically or as an autosomal dominant condition with variable expression and incomplete penetrance. Familial forms have been linked to three chromosomal loci, and loss of function mutations have been identified in the KRIT1/CCM1, MGC4607/CCM2, and PDCD10/CCM3 genes. Recently, many new pieces of data have been added to the CCM puzzle. It has been shown that the three CCM genes are expressed in neurones rather than in blood vessels. The interaction between CCM1 and CCM2, which was expected on the basis of their structure, has also been proven, suggesting a common functional pathway. Finally, in a large series of KRIT1 mutation carriers, clinical and neuroradiological features have been characterised. These data should lead to more appropriate follow up, treatment, and genetic counselling. The recent developments will also help to elucidate the precise pathogenic mechanisms leading to CCM, contributing to a better understanding of normal and pathological angiogenesis and to the development of targeted treatment.
脑海绵状血管畸形(CCM)是一种导致神经问题的血管畸形,如头痛、癫痫发作、局灶性神经功能缺损和脑出血。CCM可散发性出现,也可作为一种常染色体显性疾病出现,具有可变表达和不完全外显率。家族性形式与三个染色体位点相关,并且在KRIT1/CCM1、MGC4607/CCM2和PDCD10/CCM3基因中已鉴定出功能丧失突变。最近,CCM难题中又增添了许多新的数据。已表明这三个CCM基因在神经元中表达,而非在血管中表达。基于CCM1和CCM2的结构预期的它们之间的相互作用也已得到证实,提示存在一条共同的功能途径。最后,在一大系列KRIT1突变携带者中,已对临床和神经放射学特征进行了描述。这些数据应能带来更恰当的随访、治疗和遗传咨询。最近的进展也将有助于阐明导致CCM的确切致病机制,有助于更好地理解正常和病理性血管生成,并有助于开发靶向治疗。