Hiraide Takahiro, Suzuki Hisato, Momoi Mizuki, Shinya Yoshiki, Fukuda Keiichi, Kosaki Kenjiro, Kataoka Masaharu
Department of Cardiology, Keio University School of Medicine, Shinjuku-ku, Tokyo 160-8582, Japan.
Center for Medical Genetics, Keio University School of Medicine, Tokyo 160-8582, Japan.
Life (Basel). 2022 Apr 8;12(4):555. doi: 10.3390/life12040555.
The ring finger protein 213 gene (RNF213) encodes a 590 kDa protein that is thought to be involved in angiogenesis. This gene was first recognized as a vasculopathy-susceptibility locus through genome-wide association studies undertaken in a Japanese population, demonstrating that heterozygotes for RNF213 p.Arg4810Lys (c.14429G>A, rs112735431) had a greatly increased risk of moyamoya disease. The association of RNF213 p.Arg4810Lys as a susceptibility variant of moyamoya disease was reproduced in Korean and Chinese individuals and, later, in Caucasians. Variants of the RNF213 gene have been linked to a number of vascular diseases such as moyamoya disease, intracranial major artery stenosis, pulmonary arterial hypertension, and peripheral pulmonary artery stenosis, and have also been associated with co-occurrent diseases and vascular disease in different organs. Based on the findings that we have reported to date, our paper proposes a new concept of “RNF213-associated vascular disease” to unify these conditions with the aim of capturing patients with multiple diseases but with a common genetic background. This concept will be highly desirable for clarifying all of the diseases in the RNF213-associated vascular disease category by means of global epidemiological investigations because of the possibility of such diseases appearing asymptomatically in some patients.
环指蛋白213基因(RNF213)编码一种590 kDa的蛋白质,该蛋白质被认为参与血管生成。通过在日本人群中进行的全基因组关联研究,该基因首次被识别为一种血管病变易感基因座,研究表明RNF213 p.Arg4810Lys(c.14429G>A,rs112735431)杂合子患烟雾病的风险大大增加。RNF213 p.Arg4810Lys作为烟雾病易感变异体的关联在韩国人和中国人中得到了重现,后来在高加索人中也得到了证实。RNF213基因的变异与多种血管疾病有关,如烟雾病、颅内大动脉狭窄、肺动脉高压和外周肺动脉狭窄,还与不同器官的并发疾病和血管疾病有关。基于我们迄今为止报道的研究结果,我们的论文提出了“RNF213相关血管疾病”这一新概念,以统一这些病症,目的是识别患有多种疾病但具有共同遗传背景的患者。由于这类疾病在一些患者中可能无症状出现,通过全球流行病学调查来阐明RNF213相关血管疾病类别中的所有疾病,这一概念将非常必要。