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英国队列中耳硬化症的流行病学。

The Epidemiology of Otosclerosis in a British Cohort.

机构信息

University College London Ear Institute, University College London.

Royal National Throat Nose and Ear Hospital.

出版信息

Otol Neurotol. 2019 Jan;40(1):22-30. doi: 10.1097/MAO.0000000000002047.

DOI:10.1097/MAO.0000000000002047
PMID:30540696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6314447/
Abstract

OBJECTIVE

To analyse the epidemiology of otosclerosis in a British cohort collected between 2011 and 2017.

DESIGN

Retrospective cohort study.

SETTING

Five UK ENT Departments.

PATIENTS

Patients with surgically confirmed otosclerosis.

MAIN OUTCOME MEASURES

Questionnaire data documented family history of otosclerosis, age of onset, medical history, and information on associated risk factors for 657 patients. Pre and post-surgical pure-tone audiometry was collected for 154 of these patients.

RESULTS

The age of onset, incidence of bilateral disease, tinnitus and vertigo, a higher prevalence of women (65%) than men (35%) are similar to those reported previously for otosclerosis cohorts. No association with measles infection was detected. Patients with a family history (40%) have an earlier age of onset and a higher incidence of bilateral disease and vertigo than non-familial subjects. Pedigree analysis is consistent with an autosomal dominant inheritance with reduced penetrance being apparent in 44/91 pedigrees studied. Women who associate their hearing loss with pregnancy have an earlier age of onset than those that do not (p = 6 × 10).

CONCLUSIONS

This study confirms that otosclerosis is an early adult onset disease that is more prevalent in women than men with a large minority of patients having a family history of otosclerosis. We report new evidence to support a relationship between pregnancy and otosclerosis progression in a proportion of women. In addition, this is the first study to identify differences in severity between familial and non-familial cases of otosclerosis, highlighting the possibility that more than one etiology may be involved.

摘要

目的

分析 2011 年至 2017 年间英国队列中收集的耳硬化症的流行病学。

设计

回顾性队列研究。

地点

英国 5 个耳鼻喉科部门。

患者

手术确诊为耳硬化症的患者。

主要观察指标

657 名患者的问卷调查数据记录了耳硬化症家族史、发病年龄、病史以及与 657 名患者相关的危险因素信息。对其中 154 名患者采集了术前和术后纯音听力图。

结果

发病年龄、双侧疾病发生率、耳鸣和眩晕,女性(65%)多于男性(35%)的比例与以前报道的耳硬化症队列相似。未发现与麻疹感染有关。有家族史的患者(40%)发病年龄更早,双侧疾病和眩晕的发生率更高,而非家族性患者则没有。系谱分析符合常染色体显性遗传,44/91 个研究的系谱显示明显的不完全外显。将听力损失与妊娠相关联的女性发病年龄早于不相关的女性(p=6×10)。

结论

本研究证实,耳硬化症是一种成年早期发病的疾病,女性比男性更为常见,其中很大一部分患者有耳硬化症家族史。我们报告了新的证据支持妊娠与部分女性耳硬化症进展之间的关系。此外,这是首次研究发现家族性和非家族性耳硬化症病例之间严重程度的差异,这突出表明可能涉及不止一种病因。

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本文引用的文献

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The Audiology of Otosclerosis.耳硬化症的听力学
Otolaryngol Clin North Am. 2018 Apr;51(2):327-342. doi: 10.1016/j.otc.2017.11.007. Epub 2018 Feb 2.
2
Absence of Measles Virus Detection from Stapes of Patients with Otosclerosis.未从耳硬化症患者镫骨中检测到麻疹病毒。
Otolaryngol Head Neck Surg. 2018 Jan;158(1):158-162. doi: 10.1177/0194599817733674. Epub 2017 Oct 3.
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Stapes surgery in Sweden: evaluation of a national-based register.瑞典的镫骨手术:基于全国登记系统的评估
耳硬化症手术的功能预后
Braz J Otorhinolaryngol. 2025 Jul 11;91(6):101679. doi: 10.1016/j.bjorl.2025.101679.
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Ten years of stapes surgery in France (2013-2022). About 35368 procedures.法国十年的镫骨手术(2013 - 2022年)。约35368例手术。
Eur Arch Otorhinolaryngol. 2025 May 2. doi: 10.1007/s00405-025-09399-5.
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Association between the gene polymorphism-determined earwax properties and external auditory canal microbiota in healthy adults.健康成年人中由基因多态性决定的耳垢特性与外耳道微生物群之间的关联。
Microbiol Spectr. 2025 Feb 4;13(2):e0169824. doi: 10.1128/spectrum.01698-24. Epub 2025 Jan 16.
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Unilateral versus bilateral stapes surgery: A comparative study on auditory outcome and quality of life.单侧与双侧镫骨手术:听觉结果与生活质量的比较研究
J Otol. 2024 Apr;19(2):91-96. doi: 10.1016/j.joto.2024.06.002. Epub 2024 Oct 20.
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Classification of ossicular fixation based on a computational simulation of ossicular mobility.基于听骨活动的计算模拟对听骨固定的分类。
Sci Rep. 2024 Sep 3;14(1):20468. doi: 10.1038/s41598-024-71474-4.
8
Effectiveness of active middle ear implant placement methods in pathological conditions: basilar membrane vibration simulation.主动式中耳植入物放置方法在病理状态下的有效性:基底膜振动模拟
Front Neurol. 2024 Aug 8;15:1417711. doi: 10.3389/fneur.2024.1417711. eCollection 2024.
9
Analysis of major otosclerosis-associated variants in and genes in Polish patients.波兰患者中与耳硬化症相关的主要基因和基因变异分析。
Arch Med Sci. 2020 Sep 16;20(3):962-966. doi: 10.5114/aoms.2020.99011. eCollection 2024.
10
Incidence of Concomitant Semicircular Canal Dehiscence With Otosclerosis.耳硬化症伴半规管裂的发病率
Otol Neurotol Open. 2022 Jun 24;2(2):e012. doi: 10.1097/ONO.0000000000000012. eCollection 2022 Jun.
Eur Arch Otorhinolaryngol. 2017 Jun;274(6):2421-2427. doi: 10.1007/s00405-017-4510-2. Epub 2017 Mar 11.
4
Otosclerosis: An update on diagnosis and treatment.耳硬化症:诊断与治疗的最新进展
JAAPA. 2017 Feb;30(2):17-22. doi: 10.1097/01.JAA.0000511784.21936.1b.
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Mutations and altered expression of SERPINF1 in patients with familial otosclerosis.家族性耳硬化症患者中SERPINF1的突变与表达改变
Hum Mol Genet. 2016 Jun 15;25(12):2393-2403. doi: 10.1093/hmg/ddw106. Epub 2016 Apr 7.
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Stapes surgery: a National Survey of British Otologists.镫骨手术:英国耳科医生全国性调查
Eur Arch Otorhinolaryngol. 2016 Feb;273(2):371-9. doi: 10.1007/s00405-015-3560-6. Epub 2015 Feb 25.
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Otol Neurotol. 2012 Dec;33(9):1562-6. doi: 10.1097/MAO.0b013e31826bf19b.
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A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44.耳硬化症的一个新基因座OTSC10定位于1号染色体1q41 - 44区域。
Clin Genet. 2011 May;79(5):495-7. doi: 10.1111/j.1399-0004.2010.01576.x.
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A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.一项全基因组分析确定了与耳硬化症相关的RELN基因中的遗传变异。
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Otosclerosis associated with Ehlers-Danlos syndrome: report of a case.耳硬化症与埃勒斯-当洛综合征相关:一例报告。
Acta Otolaryngol Suppl. 2007 Dec(559):157-9. doi: 10.1080/03655230701600418.