Mouadeb Debbie Aviva, Ruckenstein Michael J
Department of Otolaryngology, University of California-Davis, Sacramento, California, USA.
Laryngoscope. 2005 May;115(5):879-83. doi: 10.1097/01.MLG.0000158666.15447.37.
This study was initiated to clarify the possible association between antiphospholipid antibodies, mediators of microthrombus formation, and sensorineural hearing loss (SNHL) of unknown origin in a large cohort of patients.
Prospective study.
The study cohort consists of 168 adult patients (>/=18 yr) referred to the University of Pennsylvania's Division of Neurotology and Balance Center for diagnosis and treatment of progressive hearing loss with or without vertigo. A comprehensive screening panel of blood tests for autoimmune and infectious diseases was applied to all patients, including testing for anticardiolipin antibodies, anti-B2 glycoprotein, and lupus anticoagulant.
Forty-two patients (25%) had at least one elevated antiphospholipid antibody marker. Twenty patients had two or more positive test results. Of the 42 patients, 64% (n = 27) met the diagnostic criteria for Meniere disease, and the remainder were diagnosed with idiopathic SNHL. Within this group of patients, 24 patients (57%) had unilateral hearing loss, and 18 (44%) had bilateral hearing loss.
These data support the hypothesis that antiphospholipid antibodies are involved in the pathogenesis of some forms of inner ear dysfunction, presumably by causing microthrombus formation in the labyrinthine vasculature. Basic science studies are required to better understand the mechanisms by which antiphospholipid antibodies mediate inner ear dysfunction. Clinical studies to evaluate the efficacy of anticoagulation in this group of patients are also required.
本研究旨在明确一大群患者中抗磷脂抗体、微血栓形成介质与不明原因的感音神经性听力损失(SNHL)之间可能存在的关联。
前瞻性研究。
研究队列由168名成年患者(≥18岁)组成,他们因进行性听力损失伴或不伴眩晕被转诊至宾夕法尼亚大学神经耳科学与平衡中心进行诊断和治疗。对所有患者进行了针对自身免疫性和感染性疾病的全面血液检查筛查,包括检测抗心磷脂抗体、抗B2糖蛋白和狼疮抗凝物。
42名患者(25%)至少有一项抗磷脂抗体标志物升高。20名患者有两项或更多阳性检测结果。在这42名患者中,64%(n = 27)符合梅尼埃病的诊断标准,其余患者被诊断为特发性SNHL。在这组患者中,24名患者(57%)有单侧听力损失,18名患者(44%)有双侧听力损失。
这些数据支持以下假设,即抗磷脂抗体参与了某些形式的内耳功能障碍的发病机制,可能是通过在迷路血管系统中形成微血栓。需要开展基础科学研究以更好地理解抗磷脂抗体介导内耳功能障碍的机制。还需要进行临床研究以评估抗凝治疗对这组患者的疗效。