遗传变异与 Moyamoya 病术后供体动脉发育的关系:RNF213 及其他莫亚莫亚血管病相关基因分析

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
Seiei Torazawa, Satoru Miyawaki, Hideaki Imai, Hiroki Hongo, Hideaki Ono, Shotaro Ogawa, Yu Sakai, Satoshi Kiyofuji, Satoshi Koizumi, Daisuke Komura, Hiroto Katoh, Shumpei Ishikawa, Nobuhito Saito
{"title":"遗传变异与 Moyamoya 病术后供体动脉发育的关系:RNF213 及其他莫亚莫亚血管病相关基因分析","authors":"Seiei Torazawa, Satoru Miyawaki, Hideaki Imai, Hiroki Hongo, Hideaki Ono, Shotaro Ogawa, Yu Sakai, Satoshi Kiyofuji, Satoshi Koizumi, Daisuke Komura, Hiroto Katoh, Shumpei Ishikawa, Nobuhito Saito","doi":"10.1007/s12975-024-01248-7","DOIUrl":null,"url":null,"abstract":"<p>Robust postoperative bypass development is a characteristic of moyamoya disease (MMD); however, genetic factors mediating this phenomenon remain incompletely understood. Therefore, we aimed to elucidate the relationship between postoperative donor artery development and genetic variants. We retrospectively enrolled 63 patients (79 hemispheres) who underwent combined revascularization surgery. Postoperative development of the superficial temporal artery (STA), middle meningeal artery, and deep temporal artery (DTA) was assessed using the caliber-change ratio determined from magnetic resonance angiography measurements. We analyzed <i>RNF213</i> and 36 other moyamoya angiopathy-related genes by whole-exome sequencing and extracted rare or damaging variants. Thirty-five participants carried <i>RNF213</i> p.Arg4810Lys (all heterozygotes), whereas 5 had <i>RNF213</i> rare variants (RVs). p.Arg4810Lys was significantly associated with postoperative DTA development, while age at surgery, hypertension, and hyperlipidemia were inversely associated. Multiple regression analysis revealed that age and p.Arg4810Lys held statistical significance (<i>P</i> = 0.044, coefficient − 0.015, 95% confidence interval (CI) − 0.029 to 0.000 and <i>P</i> = 0.001, coefficient 0.670, 95% CI 0.269 to 1.072, respectively). Those with <i>RNF213</i> RV without p.Arg4810Lys exhibited a significant trend toward poor DTA development (<i>P</i> = 0.001). Hypertension demonstrated a significant positive association with STA development, which remained significant even after multiple regression analysis (<i>P</i> = 0.001, coefficient 0.303, 95% CI 0.123 to 0.482). Following Bonferroni correction for multiple comparisons, targeted analyses of <i>RNF213</i> and 36 moyamoya angiopathy-related genes showed a significant association of only <i>RNF213</i> p.Arg4810Lys with favorable DTA development (<i>P</i> = 0.001). A comprehensive analysis of <i>RNF213</i>, considering both p.Arg4810Lys and RVs, may provide a clearer prediction of postoperative DTA development.</p>","PeriodicalId":23237,"journal":{"name":"Translational Stroke Research","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association of Genetic Variants with Postoperative Donor Artery Development in Moyamoya Disease: RNF213 and Other Moyamoya Angiopathy-Related Gene Analysis\",\"authors\":\"Seiei Torazawa, Satoru Miyawaki, Hideaki Imai, Hiroki Hongo, Hideaki Ono, Shotaro Ogawa, Yu Sakai, Satoshi Kiyofuji, Satoshi Koizumi, Daisuke Komura, Hiroto Katoh, Shumpei Ishikawa, Nobuhito Saito\",\"doi\":\"10.1007/s12975-024-01248-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Robust postoperative bypass development is a characteristic of moyamoya disease (MMD); however, genetic factors mediating this phenomenon remain incompletely understood. Therefore, we aimed to elucidate the relationship between postoperative donor artery development and genetic variants. We retrospectively enrolled 63 patients (79 hemispheres) who underwent combined revascularization surgery. Postoperative development of the superficial temporal artery (STA), middle meningeal artery, and deep temporal artery (DTA) was assessed using the caliber-change ratio determined from magnetic resonance angiography measurements. We analyzed <i>RNF213</i> and 36 other moyamoya angiopathy-related genes by whole-exome sequencing and extracted rare or damaging variants. Thirty-five participants carried <i>RNF213</i> p.Arg4810Lys (all heterozygotes), whereas 5 had <i>RNF213</i> rare variants (RVs). p.Arg4810Lys was significantly associated with postoperative DTA development, while age at surgery, hypertension, and hyperlipidemia were inversely associated. Multiple regression analysis revealed that age and p.Arg4810Lys held statistical significance (<i>P</i> = 0.044, coefficient − 0.015, 95% confidence interval (CI) − 0.029 to 0.000 and <i>P</i> = 0.001, coefficient 0.670, 95% CI 0.269 to 1.072, respectively). Those with <i>RNF213</i> RV without p.Arg4810Lys exhibited a significant trend toward poor DTA development (<i>P</i> = 0.001). Hypertension demonstrated a significant positive association with STA development, which remained significant even after multiple regression analysis (<i>P</i> = 0.001, coefficient 0.303, 95% CI 0.123 to 0.482). Following Bonferroni correction for multiple comparisons, targeted analyses of <i>RNF213</i> and 36 moyamoya angiopathy-related genes showed a significant association of only <i>RNF213</i> p.Arg4810Lys with favorable DTA development (<i>P</i> = 0.001). A comprehensive analysis of <i>RNF213</i>, considering both p.Arg4810Lys and RVs, may provide a clearer prediction of postoperative DTA development.</p>\",\"PeriodicalId\":23237,\"journal\":{\"name\":\"Translational Stroke Research\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2024-04-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translational Stroke Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s12975-024-01248-7\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Stroke Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s12975-024-01248-7","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

术后旁路的强劲发展是莫亚莫亚病(MMD)的一个特征;然而,介导这一现象的遗传因素仍不完全清楚。因此,我们旨在阐明术后供体动脉发育与遗传变异之间的关系。我们回顾性地纳入了接受联合血管重建手术的 63 例患者(79 个半球)。术后颞浅动脉(STA)、脑膜中动脉和颞深动脉(DTA)的发育情况是通过磁共振血管造影测量确定的口径变化比来评估的。我们通过全外显子组测序分析了 RNF213 和其他 36 个与 moyamoya 血管病相关的基因,并提取了罕见或损伤性变异。35名参与者携带RNF213 p.Arg4810Lys(均为杂合子),而5名参与者携带RNF213罕见变体(RVs)。p.Arg4810Lys与术后DTA的发生显著相关,而手术年龄、高血压和高脂血症则成反比。多元回归分析显示,年龄和p.Arg4810Lys具有统计学意义(分别为P = 0.044,系数- 0.015,95%置信区间(CI)- 0.029至0.000和P = 0.001,系数0.670,95%置信区间(CI)0.269至1.072)。不含 p.Arg4810Lys 的 RNF213 RV 患者表现出 DTA 发育不良的显著趋势(P = 0.001)。高血压与 STA 发育呈显著正相关,即使在进行多元回归分析后,这种关系仍然显著(P = 0.001,系数 0.303,95% CI 0.123 至 0.482)。在对多重比较进行 Bonferroni 校正后,对 RNF213 和 36 个 moyamoya 血管病相关基因进行的定向分析表明,只有 RNF213 p.Arg4810Lys 与 DTA 的良好发展有显著关联(P = 0.001)。对RNF213进行综合分析,同时考虑p.Arg4810Lys和RV,可以更清晰地预测术后DTA的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of Genetic Variants with Postoperative Donor Artery Development in Moyamoya Disease: RNF213 and Other Moyamoya Angiopathy-Related Gene Analysis

Association of Genetic Variants with Postoperative Donor Artery Development in Moyamoya Disease: RNF213 and Other Moyamoya Angiopathy-Related Gene Analysis

Robust postoperative bypass development is a characteristic of moyamoya disease (MMD); however, genetic factors mediating this phenomenon remain incompletely understood. Therefore, we aimed to elucidate the relationship between postoperative donor artery development and genetic variants. We retrospectively enrolled 63 patients (79 hemispheres) who underwent combined revascularization surgery. Postoperative development of the superficial temporal artery (STA), middle meningeal artery, and deep temporal artery (DTA) was assessed using the caliber-change ratio determined from magnetic resonance angiography measurements. We analyzed RNF213 and 36 other moyamoya angiopathy-related genes by whole-exome sequencing and extracted rare or damaging variants. Thirty-five participants carried RNF213 p.Arg4810Lys (all heterozygotes), whereas 5 had RNF213 rare variants (RVs). p.Arg4810Lys was significantly associated with postoperative DTA development, while age at surgery, hypertension, and hyperlipidemia were inversely associated. Multiple regression analysis revealed that age and p.Arg4810Lys held statistical significance (P = 0.044, coefficient − 0.015, 95% confidence interval (CI) − 0.029 to 0.000 and P = 0.001, coefficient 0.670, 95% CI 0.269 to 1.072, respectively). Those with RNF213 RV without p.Arg4810Lys exhibited a significant trend toward poor DTA development (P = 0.001). Hypertension demonstrated a significant positive association with STA development, which remained significant even after multiple regression analysis (P = 0.001, coefficient 0.303, 95% CI 0.123 to 0.482). Following Bonferroni correction for multiple comparisons, targeted analyses of RNF213 and 36 moyamoya angiopathy-related genes showed a significant association of only RNF213 p.Arg4810Lys with favorable DTA development (P = 0.001). A comprehensive analysis of RNF213, considering both p.Arg4810Lys and RVs, may provide a clearer prediction of postoperative DTA development.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Translational Stroke Research
Translational Stroke Research CLINICAL NEUROLOGY-NEUROSCIENCES
CiteScore
13.80
自引率
4.30%
发文量
130
审稿时长
6-12 weeks
期刊介绍: Translational Stroke Research covers basic, translational, and clinical studies. The Journal emphasizes novel approaches to help both to understand clinical phenomenon through basic science tools, and to translate basic science discoveries into the development of new strategies for the prevention, assessment, treatment, and enhancement of central nervous system repair after stroke and other forms of neurotrauma. Translational Stroke Research focuses on translational research and is relevant to both basic scientists and physicians, including but not restricted to neuroscientists, vascular biologists, neurologists, neuroimagers, and neurosurgeons.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信