| Literature DB >> 31060437 |
Teppei Kamimura1, Shuhei Okazaki1,2, Takaaki Morimoto3,4, Hatasu Kobayashi4,5, Kouji Harada4, Tsutomu Tomita6, Aya Higashiyama6, Takeshi Yoshimoto1, Jun C Takahashi7, Jyoji Nakagawara7, Masatoshi Koga8, Kazunori Toyoda8, Hirofumi Maruyama3, Akio Koizumi4, Masafumi Ihara1.
Abstract
Background and Purpose- The ring finger protein 213 gene ( RNF213) is a susceptibility gene for moyamoya disease and large-artery ischemic stroke in East Asia. We examined the prevalence and correlates of the RNF213 p.R4810K variant in patients with early-onset ischemic stroke in a Japanese single-center cohort. Methods- We analyzed 70 early-onset stroke patients with intracranial arterial stenosis who developed a noncardioembolic stroke or transient ischemic attack from 20 to 60 years of age. Patients with moyamoya disease were excluded. Results- The RNF213 p.R4810K variant was found in 17 patients (24%), and more often in women than men (38% versus 16%, odds ratio 3.3; 95% CI, 1.1-10.2, P=0.04). The variant was identified in 35% of patients with stenosis in the M1 segment of the middle cerebral artery or the A1 segment of the anterior cerebral artery (odds ratio, 25.0; 95% CI, 1.4-438; P<0.01) but in only one patient (9%) with intracranial posterior circulation stenosis. Conventional atherosclerotic risk factors did not differ between variant carriers and noncarriers. Conclusions- The RNF213 p.R4810K variant is common in early-onset ischemic stroke with anterior circulation stenosis in Japan. Further investigation of the RNF213 gene will provide new insights into pathogenetic mechanisms of early-onset stroke.Entities:
Keywords: Japan; atherosclerosis; moyamoya disease; prevalence; risk factor
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Year: 2019 PMID: 31060437 DOI: 10.1161/STROKEAHA.118.024712
Source DB: PubMed Journal: Stroke ISSN: 0039-2499 Impact factor: 7.914