EAS(电声刺激)候选者的遗传背景

S. Usami, Maiko Miyagawa, N. Suzuki, Hideaki Moteki, S. Nishio, Y. Takumi, S. Iwasaki
{"title":"EAS(电声刺激)候选者的遗传背景","authors":"S. Usami, Maiko Miyagawa, N. Suzuki, Hideaki Moteki, S. Nishio, Y. Takumi, S. Iwasaki","doi":"10.3109/16513860903565214","DOIUrl":null,"url":null,"abstract":"Abstract There is a certain number of patients with so-called ski-slope hearing loss, in which there is good hearing for lower frequencies in spite of little/no hearing in high frequencies. EAS (electric-acoustic stimulation) has recently been introduced for such patients with residual hearing at lower frequencies. Ski-slope hearing loss can have either a progressive nature or can be rather stable; therefore, decisions regarding timing of surgery are sometimes hampered. One advantage of genetic testing is that the possible prognosis for hearing, i.e. progressive or not, can be predicted for individual patients. The present study was performed to estimate the frequency of ski-slope hearing loss and investigate the genetic background of candidates for EAS. Using a 2587 subject DNA database of sensorineural hearing loss patients, 1) frequency of patients with ski-slope hearing loss, 2) their clinical features including inheritance mode, onset ages, and progression, and 3) involvement of four common genes with mutations in Japanese hearing loss patients, were evaluated. One hundred and fifty-one out of 2587 subjects fulfilled the audiological criteria for EAS. The frequency of patients possibly meeting the criteria for EAS was estimated to be 9.1% by restriction to probands only (139/1520). Various inheritance modes and onset ages were noted, with earlier onset in the patients with sporadic/recessive inheritance mode. Progressiveness was recognized in 56% of the patients. Genetic analysis identified mutations in 26.6% of the patients, including the mitochondrial 1555A>G mutation, and mutations in SLC26A4, CDH23, and GJB2 genes, suggesting that at the least, these four genes may be involved in a certain group of patients, but also leaving possible genetic causes in the majority of the patients undetermined. As most of the patients showed a progressive nature in their hearing, genetic testing adds important additional information for candidates for EAS.","PeriodicalId":88223,"journal":{"name":"Audiological medicine","volume":"5 1","pages":"28 - 32"},"PeriodicalIF":0.0000,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"18","resultStr":"{\"title\":\"Genetic background of candidates for EAS (Electric-Acoustic Stimulation)\",\"authors\":\"S. Usami, Maiko Miyagawa, N. Suzuki, Hideaki Moteki, S. Nishio, Y. Takumi, S. Iwasaki\",\"doi\":\"10.3109/16513860903565214\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract There is a certain number of patients with so-called ski-slope hearing loss, in which there is good hearing for lower frequencies in spite of little/no hearing in high frequencies. EAS (electric-acoustic stimulation) has recently been introduced for such patients with residual hearing at lower frequencies. Ski-slope hearing loss can have either a progressive nature or can be rather stable; therefore, decisions regarding timing of surgery are sometimes hampered. One advantage of genetic testing is that the possible prognosis for hearing, i.e. progressive or not, can be predicted for individual patients. The present study was performed to estimate the frequency of ski-slope hearing loss and investigate the genetic background of candidates for EAS. Using a 2587 subject DNA database of sensorineural hearing loss patients, 1) frequency of patients with ski-slope hearing loss, 2) their clinical features including inheritance mode, onset ages, and progression, and 3) involvement of four common genes with mutations in Japanese hearing loss patients, were evaluated. One hundred and fifty-one out of 2587 subjects fulfilled the audiological criteria for EAS. The frequency of patients possibly meeting the criteria for EAS was estimated to be 9.1% by restriction to probands only (139/1520). Various inheritance modes and onset ages were noted, with earlier onset in the patients with sporadic/recessive inheritance mode. Progressiveness was recognized in 56% of the patients. Genetic analysis identified mutations in 26.6% of the patients, including the mitochondrial 1555A>G mutation, and mutations in SLC26A4, CDH23, and GJB2 genes, suggesting that at the least, these four genes may be involved in a certain group of patients, but also leaving possible genetic causes in the majority of the patients undetermined. As most of the patients showed a progressive nature in their hearing, genetic testing adds important additional information for candidates for EAS.\",\"PeriodicalId\":88223,\"journal\":{\"name\":\"Audiological medicine\",\"volume\":\"5 1\",\"pages\":\"28 - 32\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2010-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"18\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Audiological medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3109/16513860903565214\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Audiological medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/16513860903565214","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 18

摘要

摘要有一定数量的所谓“滑坡性听力损失”患者,即低频听力良好,高频听力很少或没有。EAS(电声刺激)最近被引入到这类患者的低频率残余听力。滑雪坡性听力损失可以是进行性的,也可以是相当稳定的;因此,关于手术时机的决定有时会受到阻碍。基因检测的一个优点是,听力的可能预后,即进展与否,可以预测个别患者。本研究旨在估计滑雪坡听力损失的频率,并调查EAS候选人的遗传背景。利用2587例感音神经性听力损失患者DNA数据库,对滑雪坡性听力损失患者的发病频率,遗传模式、发病年龄、进展等临床特征,以及日本听力损失患者中4种常见基因突变的参与情况进行了评估。2587名受试者中有151名符合EAS的听力学标准。仅以先证为限,可能符合EAS标准的患者频率估计为9.1%(139/1520)。不同的遗传方式和发病年龄,以散发/隐性遗传方式患者发病早。56%的患者病情进展。遗传分析发现26.6%的患者发生突变,包括线粒体1555A>G突变,SLC26A4、CDH23和GJB2基因突变,这表明至少这四个基因可能与某一组患者有关,但大多数患者可能的遗传原因尚不确定。由于大多数患者的听力表现出进行性,基因检测为EAS候选人提供了重要的额外信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Genetic background of candidates for EAS (Electric-Acoustic Stimulation)
Abstract There is a certain number of patients with so-called ski-slope hearing loss, in which there is good hearing for lower frequencies in spite of little/no hearing in high frequencies. EAS (electric-acoustic stimulation) has recently been introduced for such patients with residual hearing at lower frequencies. Ski-slope hearing loss can have either a progressive nature or can be rather stable; therefore, decisions regarding timing of surgery are sometimes hampered. One advantage of genetic testing is that the possible prognosis for hearing, i.e. progressive or not, can be predicted for individual patients. The present study was performed to estimate the frequency of ski-slope hearing loss and investigate the genetic background of candidates for EAS. Using a 2587 subject DNA database of sensorineural hearing loss patients, 1) frequency of patients with ski-slope hearing loss, 2) their clinical features including inheritance mode, onset ages, and progression, and 3) involvement of four common genes with mutations in Japanese hearing loss patients, were evaluated. One hundred and fifty-one out of 2587 subjects fulfilled the audiological criteria for EAS. The frequency of patients possibly meeting the criteria for EAS was estimated to be 9.1% by restriction to probands only (139/1520). Various inheritance modes and onset ages were noted, with earlier onset in the patients with sporadic/recessive inheritance mode. Progressiveness was recognized in 56% of the patients. Genetic analysis identified mutations in 26.6% of the patients, including the mitochondrial 1555A>G mutation, and mutations in SLC26A4, CDH23, and GJB2 genes, suggesting that at the least, these four genes may be involved in a certain group of patients, but also leaving possible genetic causes in the majority of the patients undetermined. As most of the patients showed a progressive nature in their hearing, genetic testing adds important additional information for candidates for EAS.
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
自引率
0.00%
发文量
0
期刊最新文献
Referees Morphological and functional structure of the inner ear: Its relation to Ménière's disease Medical therapy in Ménière's disease Simon Dafydd Glyn Stephens, Professor of Audiological Medicine Ménière's disorder: A short history
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1