Department of Clinical and Biological Sciences, University of Torino, 10043 Orbassano, Torino, Italy; CCM Italia Research Network, National Coordination Center at the Department of Clinical and Biological Sciences, University of Torino, 10043 Orbassano, Torino, Italy.
Free Radic Biol Med. 2021 Aug 20;172:403-417. doi: 10.1016/j.freeradbiomed.2021.06.021. Epub 2021 Jun 24.
Cerebral Cavernous Malformation (CCM) is a cerebrovascular disease of genetic origin affecting 0.5% of the population and characterized by abnormally enlarged and leaky capillaries that predispose to seizures, neurological deficits, and intracerebral hemorrhage (ICH). CCM occurs sporadically or is inherited as dominant condition with incomplete penetrance and highly variable expressivity. Three disease genes have been identified: KRIT1 (CCM1), CCM2 and CCM3. Previous results demonstrated that loss-of-function mutations of CCM genes cause pleiotropic effects, including defective autophagy, altered reactive oxygen species (ROS) homeostasis, and enhanced sensitivity to oxidative stress and inflammatory events, suggesting a novel unifying pathogenetic mechanism, and raising the possibility that CCM disease onset and severity are influenced by the presence of susceptibility and modifier genes. Consistently, genome-wide association studies (GWAS) in large and homogeneous cohorts of patients sharing the familial form of CCM disease and identical mutations in CCM genes have led to the discovery of distinct genetic modifiers of major disease severity phenotypes, such as development of numerous and large CCM lesions, and susceptibility to ICH. This review deals with the identification of genetic modifiers with a significant impact on inter-individual variability in CCM disease onset and severity, including highly polymorphic genes involved in oxidative stress, inflammatory and immune responses, such as cytochrome P450 monooxygenases (CYP), matrix metalloproteinases (MMP), and Toll-like receptors (TLR), pointing to their emerging prognostic value, and opening up new perspectives for risk stratification and personalized medicine strategies.
脑静脉畸形(CCM)是一种遗传性脑血管疾病,影响人群的 0.5%,其特征是异常扩大和渗漏的毛细血管,易导致癫痫发作、神经功能缺损和颅内出血(ICH)。CCM 是散发性的,也可以作为不完全外显和表现度高度可变的显性遗传疾病。已经确定了三个疾病基因:KRIT1(CCM1)、CCM2 和 CCM3。先前的研究结果表明,CCM 基因的功能丧失突变会导致多种表型效应,包括自噬缺陷、活性氧(ROS)稳态改变和对氧化应激和炎症事件的敏感性增强,这提示了一种新的统一发病机制,并提出了 CCM 疾病的发病和严重程度可能受易感性和修饰基因的影响。一致地,在具有 CCM 疾病家族形式和 CCM 基因相同突变的大而同质的患者队列中进行的全基因组关联研究(GWAS)导致了对主要疾病严重程度表型的不同遗传修饰因子的发现,例如许多和大的 CCM 病变的发展,以及对 ICH 的易感性。这篇综述涉及对个体间 CCM 疾病发病和严重程度的个体差异具有显著影响的遗传修饰因子的鉴定,包括参与氧化应激、炎症和免疫反应的高度多态性基因,如细胞色素 P450 单加氧酶(CYP)、基质金属蛋白酶(MMP)和 Toll 样受体(TLR),指出了它们新兴的预后价值,并为风险分层和个体化医学策略开辟了新的视角。