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本文引用的文献

1
The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline.RUSH2A 研究:最佳矫正视力、全视野视网膜电图幅度和全视野刺激阈值的基线值。
Transl Vis Sci Technol. 2020 Oct 8;9(11):9. doi: 10.1167/tvst.9.11.9. eCollection 2020 Oct.
2
COVID-19 and anosmia: A review based on up-to-date knowledge.新型冠状病毒肺炎与嗅觉障碍:基于最新知识的综述。
Am J Otolaryngol. 2020 Sep-Oct;41(5):102581. doi: 10.1016/j.amjoto.2020.102581. Epub 2020 Jun 2.
3
Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity.RUSH2A 研究中的基线视野结果:相关因素及其与其他疾病严重程度测量指标的相关性。
Am J Ophthalmol. 2020 Nov;219:87-100. doi: 10.1016/j.ajo.2020.05.024. Epub 2020 May 22.
4
Clinical validation of the olfactory detection threshold module of the Snap & Sniff® olfactory test system.临床验证 Snap & Sniff®嗅觉测试系统的嗅觉检测阈值模块。
Int Forum Allergy Rhinol. 2019 Sep;9(9):986-992. doi: 10.1002/alr.22377. Epub 2019 Jul 8.
5
A pilot investigation of audiovisual processing and multisensory integration in patients with inherited retinal dystrophies.遗传性视网膜营养不良患者视听处理与多感官整合的初步研究。
BMC Ophthalmol. 2017 Dec 7;17(1):240. doi: 10.1186/s12886-017-0640-y.
6
Accelerated age-related olfactory decline among type 1 Usher patients.1型尤塞氏综合征患者中与年龄相关的嗅觉加速衰退。
Sci Rep. 2016 Jun 22;6:28309. doi: 10.1038/srep28309.
7
Impact of the Usher syndrome on olfaction.乌谢尔综合征对嗅觉的影响。
Hum Mol Genet. 2016 Feb 1;25(3):524-33. doi: 10.1093/hmg/ddv490. Epub 2015 Nov 29.
8
A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants.对非综合征性USH2A视网膜病变患者进行的详细临床和分子调查揭示了致病变异的等位基因层次结构。
Eur J Hum Genet. 2015 Oct;23(10):1318-27. doi: 10.1038/ejhg.2014.283. Epub 2015 Feb 4.
9
ISCEV Standard for full-field clinical electroretinography (2015 update).国际临床视觉电生理学会全视野临床视网膜电图标准(2015年更新版)
Doc Ophthalmol. 2015 Feb;130(1):1-12. doi: 10.1007/s10633-014-9473-7. Epub 2014 Dec 14.
10
Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.尤塞氏综合征:听力丧失、视网膜变性及相关异常。
Biochim Biophys Acta. 2015 Mar;1852(3):406-20. doi: 10.1016/j.bbadis.2014.11.020. Epub 2014 Dec 4.

USH2A 相关视网膜变性患者的听觉和嗅觉发现-USH2A 相关视网膜变性自然史研究(RUSH2A)中的进展率的基线发现。

Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A).

机构信息

Duke Eye Center, Department of Ophthalmology, Duke University Medical School, Durham, North Carolina, USA.

National Institute on Deafness and Other Communication Disorders, Bethesda, Maryland, USA.

出版信息

Am J Med Genet A. 2021 Dec;185(12):3717-3727. doi: 10.1002/ajmg.a.62437. Epub 2021 Jul 30.

DOI:10.1002/ajmg.a.62437
PMID:34331386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8717864/
Abstract

Sensorineural hearing loss (SNHL) is characteristic of Usher syndrome type 2 (USH2), but less is known about SNHL in nonsyndromic autosomal recessive retinitis pigmentosa (ARRP) and olfaction in USH2A-associated retinal degeneration. The Rate of Progression of USH2A-related Retinal Degeneration (RUSH2A) is a natural history study that enrolled 127 participants, 80 with USH2 and 47 with ARRP. Hearing was measured by pure-tone thresholds and word recognition scores, and olfaction by the University of Pennsylvania Smell Identification Test (UPSIT). SNHL was moderate in 72% of USH2 participants and severe or profound in 25%, while 9% of ARRP participants had moderate adult-onset SNHL. Pure-tone thresholds worsened with age in ARRP but not in USH2 participants. The degree of SNHL was not associated with other participant characteristics in either USH2 or ARRP. Median pure-tone thresholds in ARRP participants were significantly higher than the normative population (p < 0.001). Among 14 USH2 participants reporting newborn hearing screening results, 7 reported passing. Among RUSH2A participants, 7% had mild microsmia and 5% had moderate or severe microsmia. Their mean (±SD) UPSIT score was 35 (±3), similar to healthy controls (34 [±3]; p = 0.39). Olfaction differed by country (p = 0.02), but was not significantly associated with clinical diagnosis, age, gender, race/ethnicity, smoking status, visual measures, or hearing. Hearing loss in USH2A-related USH2 did not progress with age. ARRP patients had higher pure-tone thresholds than normal. Newborn hearing screening did not identify all USH2A-related hearing loss. Olfaction was not significantly worse than normal in participants with USH2A-related retinal degeneration.

摘要

感音神经性听力损失 (SNHL) 是 2 型 Usher 综合征 (USH2) 的特征,但对于非综合征性常染色体隐性视网膜色素变性 (ARRP) 和 USH2A 相关视网膜变性中的嗅觉知之甚少。USH2A 相关视网膜变性的进展速度 (RUSH2A) 是一项自然史研究,共纳入 127 名参与者,其中 80 名患有 USH2,47 名患有 ARRP。听力通过纯音阈值和言语识别评分进行测量,嗅觉通过宾夕法尼亚大学嗅觉识别测试 (UPSIT) 进行测量。72%的 USH2 参与者有中度 SNHL,25%为重度或极重度 SNHL,而 9%的 ARRP 参与者有中度成人发病 SNHL。ARRP 参与者的纯音阈值随年龄增长而恶化,但 USH2 参与者则不然。无论在 USH2 还是 ARRP 中,SNHL 的严重程度都与其他参与者特征无关。ARRP 参与者的中位数纯音阈值明显高于正常人群 (p < 0.001)。在报告新生儿听力筛查结果的 14 名 USH2 参与者中,有 7 名通过。在 RUSH2A 参与者中,有 7%有轻度嗅觉障碍,5%有中度或重度嗅觉障碍。他们的 UPSIT 平均得分 (±SD) 为 35 (±3),与健康对照组相似 (34 [±3];p = 0.39)。嗅觉因国家而异 (p = 0.02),但与临床诊断、年龄、性别、种族/民族、吸烟状况、视力测量或听力无关。USH2A 相关 USH2 中的听力损失不会随年龄增长而进展。ARRP 患者的纯音阈值高于正常。新生儿听力筛查并未发现所有 USH2A 相关听力损失。在 USH2A 相关视网膜变性患者中,嗅觉功能并未明显下降。