Tsuzuki Nobuyoshi, Masuda Kanako, Yamanobe Yoshiharu, Mizuno Kohei, Ozawa Hiroyuki, Wasano Koichiro
National Institute of Sensory Organs, NHO Tokyo Medical Center, Higashigaoka, Meguro, Tokyo, Japan.
Department of Otolaryngology, NHO Tokyo Medical Center, Higashigaoka, Meguro, Tokyo, Japan.
Otol Neurotol. 2025 Jun 1;46(5):616-620. doi: 10.1097/MAO.0000000000004473. Epub 2025 Feb 20.
Although the specific pathogenesis of idiopathic sudden sensorineural hearing loss (ISSNHL) remains unknown, vascular impairment is one of the leading causes of ISSNHL. Establishing diagnostic criteria for ISSNHL due to vascular impairment is essential. We hypothesized that isolated posterior semicircular canal dysfunction (IPSCD) in ISSNHL patients results from infarction of the vestibulo-cochlear artery (VCA). The aim of this preliminary retrospective study is to identify possible diagnostic characteristics of ISSNHL patients with IPSCD.
Seventeen ISSNHL patients were enrolled. They underwent video head impulse testing within 28 days of ISSNHL onset between September 2019 and November 2023. We obtained patient characteristics and clinical information, including results of audiometric and balance function tests. Eligible patients were divided into two groups according to the presence or absence of IPSCD. Patient characteristics and clinical information of the two groups were compared.
Of the 17 ISSNHL patients included, 6 had IPSCD. Compared to the 11 patients without IPSCD, the 6 patients with IPSCD had significantly more coronary artery disease (odds ratio, infinite; p = 0.03) and had regularly used antithrombotic medications (odds ratio, infinite; p < 0.01). The audiogram shapes of the six ISSNHL-IPSCD patients were profound, flat, or high-frequency descending forms.
Given that VCA impairment is associated with profound, flat, and high-frequency hearing loss and consistent with the arterial anatomy of the inner ear, ISSNHL-IPSCD patients are more likely to have vascular impairment. Conducting trials that target ISSNHL-IPSCD patients may lead to the discovery of new and effective treatments for ISSNHL.
尽管特发性突发性感音神经性听力损失(ISSNHL)的具体发病机制尚不清楚,但血管损伤是ISSNHL的主要病因之一。建立血管损伤所致ISSNHL的诊断标准至关重要。我们推测,ISSNHL患者的孤立后半规管功能障碍(IPSCD)是由前庭蜗动脉(VCA)梗死引起的。这项初步回顾性研究的目的是确定IPSCD的ISSNHL患者可能的诊断特征。
纳入17例ISSNHL患者。他们在2019年9月至2023年11月期间ISSNHL发病的28天内接受了视频头脉冲测试。我们获取了患者的特征和临床信息,包括听力测定和平衡功能测试结果。符合条件的患者根据是否存在IPSCD分为两组。比较两组患者的特征和临床信息。
在纳入的17例ISSNHL患者中,6例有IPSCD。与11例无IPSCD的患者相比,6例有IPSCD的患者患冠状动脉疾病的比例显著更高(比值比,无穷大;p = 0.03),并且经常使用抗血栓药物(比值比,无穷大;p < 0.01)。6例ISSNHL-IPSCD患者的听力图形状为重度、平坦或高频下降型。
鉴于VCA损伤与重度、平坦和高频听力损失相关,且与内耳的动脉解剖结构一致,ISSNHL-IPSCD患者更有可能存在血管损伤。针对ISSNHL-IPSCD患者进行试验可能会发现治疗ISSNHL的新的有效方法。