RNF213 Variant and Infectious Burden Associated With Intracranial Artery Stenosis in Moyamoya Disease

作者：Chaofan Zeng, Peicong Ge, Zihan Yin, Junlin Lu, Xiaofan Yu, Junsheng Li, Yuanren Zhai, Chenglong Liu, Qiheng He, Wei Liu, Jia Wang, Xingju Liu, Xun Ye, Qian Zhang, Rong Wang, Yan Zhang, Dong Zhang, Jizong Zhao · 发表于：Journal of the American Heart Association · 年份：2025 · DOI：10.1161/jaha.124.036830 · 被引用次数：7 · 研究领域：Moyamoya disease diagnosis and treatment、Neurological Complications and Syndromes、Cerebrovascular and genetic disorders

Background The mechanisms driving the progression of moyamoya disease (MMD) remain unrecognized. There is evidence suggesting that genetic and environmental factors may be associated with intracranial artery stenosis. Here, we aimed to investigate the characteristics of infectious exposure and the association of the RNF213 (RING finger protein 213) variant and infectious burden (IB) with intracranial artery stenosis of MMD. Methods and Results We prospectively recruited 275 patients with MMD. Participants underwent RNF213 p.R4810K sequencing. Serum antibody titers of herpes simplex virus, cytomegalovirus, toxoplasma, rubella virus, and Epstein‐Barr virus were assessed and combined into an IB score. The degree of intracranial artery stenosis was measured by using the Willis narrowing score (WNS), which was then dichotomized as mild and severe. Multivariate regression analyses were performed to analyze variables associated with severe WNS. Patients with the RNF213 variant had a higher risk of severe WNS than wild‐type individuals ( P =0.003). Patients with MMD with severe WNS showed an increased level of IB score ( P <0.001). The RNF213 variant (odds ratio [OR], 2.832 [95% CI, 1.347–5.955]; P =0.006) and IB score (OR, 1.771 [95% CI, 1.286–2.439]; P <0.001) were significantly associated with severe WNS after adjusting for covariates. Furthermore, the associations between IB score and severe WNS were more prominent among patients with modifiable risk factors of elevated bod...