Rodríguez-Valiente Antonio, Álvarez-Montero Óscar, Górriz-Gil Carmen, García-Berrocal José Ramón
Department of Otorhinolaryngology, Puerta de Hierro University Hospital, Majadahonda, Madrid, Spain.
Department of Otorhinolaryngology, Puerta de Hierro University Hospital, Majadahonda, Madrid, Spain.
Acta Otorrinolaringol Esp (Engl Ed). 2019 Jul-Aug;70(4):229-234. doi: 10.1016/j.otorri.2018.06.001. Epub 2018 Aug 11.
This is the first report dealing with immune-mediated inner ear disease (IMIED) hearing loss in a group of patients affected with autoimmune thyroid disease (AITD), whose treatment required corticosteroids, despite being treated with levothyroxine. Immunopathology linking the inner ear and the thyroid gland is also presented.
A total of 220 patients were selected with sensorineural hearing loss (SNHL) of causes other than presbycusis. Audiometry was performed and pure tone average was calculated before and after treatment with corticosteroids.
Eighty-four (84) patients had SNHL of autoimmune origin, and 15 patients were diagnosed with AITD (Hashimoto's disease). Bilateral hearing loss was observed in 10 patients (66.5%). Sudden sensorineural hearing loss was the most frequent clinical form of presentation. Nine patients showed a hearing recovery greater than 10dB after corticosteroid treatment.
Acquired hypothyroidism is thought to affect hearing due to different mechanisms. Although specific hormonal therapy may improve peripheral or central auditory disorders associated with hypothyroidism, the presence of IMIED in AITD patients requires another approach. Altered immune regulatory mechanisms involving Treg cells and CD4+CD45RO cells have been suggested in patients with AITD and IMIED. In the present study, although all the patients with hypothyroidism and subclinical hypothyroidism were being treated with levothyroxine, immune-mediated hearing loss was observed. Therapy with corticosteroids could achieve hearing recovery. Since inner ear and thyroid gland share possible antigen targets, we highlight the existence of IMIED in AITD patients and the importance of implementing appropriate therapy with corticosteroids.
这是首篇关于自身免疫性甲状腺疾病(AITD)患者中免疫介导性内耳疾病(IMIED)听力损失的报告,这些患者尽管接受了左甲状腺素治疗,但治疗仍需使用皮质类固醇。文中还介绍了将内耳与甲状腺联系起来的免疫病理学。
共选取了220例非老年性聋原因所致的感音神经性听力损失(SNHL)患者。在使用皮质类固醇治疗前后进行听力测定并计算纯音平均听阈。
84例患者的SNHL源于自身免疫,15例患者被诊断为AITD(桥本氏病)。10例患者(66.5%)出现双侧听力损失。突发性感音神经性听力损失是最常见的临床表现形式。9例患者在接受皮质类固醇治疗后听力恢复超过10dB。
后天性甲状腺功能减退被认为通过不同机制影响听力。尽管特定的激素治疗可能改善与甲状腺功能减退相关的外周或中枢听觉障碍,但AITD患者中IMIED的存在需要另一种治疗方法。AITD和IMIED患者中存在涉及调节性T细胞和CD4+CD45RO细胞的免疫调节机制改变。在本研究中,尽管所有甲状腺功能减退和亚临床甲状腺功能减退患者都在接受左甲状腺素治疗,但仍观察到免疫介导的听力损失。皮质类固醇治疗可实现听力恢复。由于内耳和甲状腺可能共享抗原靶点,我们强调AITD患者中IMIED的存在以及实施适当皮质类固醇治疗的重要性。