The Incidence and Prognosis of Positive Autoimmune Laboratory Markers in Idiopathic Sudden Sensorineural Hearing Loss: A National Database Study.

IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY
Otology & Neurotology Pub Date : 2025-08-01 Epub Date: 2025-01-22 DOI:10.1097/MAO.0000000000004415
Adam S Vesole, Joseph T Breen
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引用次数: 0

Abstract

Objective: To identify the incidence of positive autoimmune laboratory markers in idiopathic sudden sensorineural hearing loss (iSSNHL) and its impact on hearing prognosis.

Study design: Retrospective cohort database study.

Setting: A collaborative national database (TriNetX) sourced from 79 large healthcare organizations in the United States.

Patients: Adults (≥18 years old) diagnosed with iSSNHL (ICD-10 H91.2) treated with systemic steroids.

Interventions: Autoimmune laboratory markers and salvage intratympanic (IT) steroids for SSNHL (CPT 69801).

Main outcome measures: 1) Positivity of autoimmune laboratory markers-rheumatoid factor (RF), ANCA, DNA double strand antibody (Ab), Sjogren syndrome A and B Abs, SCL-70 Ab, cardiolipin IgG Ab, Jo-1 Ab, ANA, mitochondria Ab. 2) Percent of patients that underwent salvage IT steroids, cochlear implantation, or hearing aid evaluation-all utilized as a proxy for hearing outcomes.

Results: Subjects with iSSNHL who had autoimmune testing (n = 17,413) were marginally more likely to be positive for at least one autoimmune laboratory marker compared to subjects without iSSNHL (n = 17,413; 23.0% vs. 21.4%, p = 0.0006). Statistical significance was lost after removing nonspecific autoimmune markers, however. Of those with iSSNHL who received systemic steroid treatment, subjects with positive autoimmune markers (n = 5,153) versus negative autoimmune markers (n = 5,153) underwent similar rates of salvage IT steroids (7.1% vs. 7.8%, p = 0.154), hearing aid evaluation (2.76% vs 2.47%, p = 0.354), and cochlear implantation (1.65% vs. 1.69%, p = 0.878).

Conclusions: Patients with iSSNHL have a marginally higher incidence of nonspecific positive autoimmune laboratory markers compared to those without iSSNHL; however, the presence of these markers does not predict treatment response or prognosis. Specifically, autoimmune markers did not predict the need for salvage IT steroids, nor CI and hearing aid use in iSSNHL. Autoimmune laboratory testing may be useful in iSSNHL patients with additional symptoms suspicious for an autoimmune disorder; however, a generalized screening is not recommended as it is unlikely to alter management or prognosis.

特发性突发性感音神经性听力损失中阳性自身免疫实验室标志物的发生率和预后:一项国家数据库研究。
目的:探讨特发性突发性感音神经性听力损失(iSSNHL)患者自身免疫实验室阳性标志物的发生率及其对听力预后的影响。研究设计:回顾性队列数据库研究。环境:来自美国79个大型医疗保健组织的协作性国家数据库(TriNetX)。患者:成人(≥18岁)诊断为iSSNHL (ICD-10 H91.2),接受全身性类固醇治疗。干预措施:自身免疫实验室标志物和挽救性鼓室内(IT)类固醇治疗SSNHL (CPT 69801)。主要观察指标:1)自身免疫实验室标志物——类风湿因子(RF)、ANCA、DNA双链抗体(Ab)、干燥综合征A和B抗体、SCL-70抗体、心磷脂IgG抗体、Jo-1抗体、ANA、线粒体抗体的阳性。2)接受补救性IT类固醇、人工耳蜗植入或助听器评估的患者的百分比——所有这些都被用作听力结果的替代指标。结果:有自身免疫检测的iSSNHL患者(n = 17,413)至少有一种自身免疫实验室标志物阳性的可能性比没有iSSNHL的患者(n = 17,413;23.0% vs. 21.4%, p = 0.0006)。然而,在去除非特异性自身免疫标记后,统计学意义丧失。在接受全身类固醇治疗的iSSNHL患者中,自身免疫标记物阳性(n = 5153)和自身免疫标记物阴性(n = 5153)的患者接受补救性IT类固醇治疗的比例相似(7.1%对7.8%,p = 0.154),助听器评估(2.76%对2.47%,p = 0.354)和人工耳廓植入(1.65%对1.69%,p = 0.878)。结论:与非iSSNHL患者相比,iSSNHL患者非特异性阳性自身免疫实验室标志物的发生率略高;然而,这些标志物的存在并不能预测治疗反应或预后。具体来说,自身免疫标记不能预测iSSNHL患者是否需要补救性IT类固醇,也不能预测CI和助听器的使用。自身免疫实验室检测可能对有疑似自身免疫性疾病附加症状的iSSNHL患者有用;然而,不建议进行全面筛查,因为它不太可能改变治疗或预后。
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来源期刊
Otology & Neurotology
Otology & Neurotology 医学-耳鼻喉科学
CiteScore
3.80
自引率
14.30%
发文量
509
审稿时长
3-6 weeks
期刊介绍: ​​​​​Otology & Neurotology publishes original articles relating to both clinical and basic science aspects of otology, neurotology, and cranial base surgery. As the foremost journal in its field, it has become the favored place for publishing the best of new science relating to the human ear and its diseases. The broadly international character of its contributing authors, editorial board, and readership provides the Journal its decidedly global perspective.
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