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Sleep Disturbance and Altered Expression of Circadian Clock Genes in Patients With Sudden Sensorineural Hearing Loss

机译:突然的感音神经性听力丧失患者的睡眠障碍和昼夜节律基因表达的改变

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摘要

The cause of sudden sensorineural hearing loss (SSNHL) remains unclear and therefore it is often considered as idiopathic. Sleep disturbance has been linked to SSNHL and circadian rhythm disruption, but the link between circadian rhythm disruption and SSNHL has never been investigated.In this study, we surveyed the sleep quality of 38 patients with SSNHL using a simple insomnia sleep questionnaire. The expression of circadian clock genes in peripheral blood (PB) leukocytes from 38 patients with SSNHL and 71 healthy subjects was accessed using real-time quantitative reverse transcriptase-polymerase chain reaction and validated using immunocytochemical staining.We found that 61.8% of patients with SSNHL suffered from insomnia before the insult of hearing loss. Besides, significantly decreased expression of PER1, CRY1, CRY2, CLOCK, BMAL1, and CKlε was found in PB leukocytes of patients with SSNHL when compared with healthy subjects. SSNHL patients with vertigo had significantly lower expression of CRY1 and CKlε than patients without vertigo symptoms. Our results imply the association of sleep disturbance and disrupted circadian rhythm in SSNHL.
机译:突然的感音神经性听力丧失(SSNHL)的原因尚不清楚,因此通常被认为是特发性的。睡眠障碍与SSNHL和昼夜节律紊乱有关,但从未研究过昼夜节律紊乱与SSNHL之间的联系。在这项研究中,我们使用简单的失眠睡眠问卷调查了38例SSNHL的睡眠质量。实时定量逆转录酶-聚合酶链反应检测38例SSNHL患者和71例健康受试者外周血(PB)白细胞中昼夜节律基因的表达,并通过免疫细胞化学染色验证,发现61.8%的SSNHL患者在遭受听力损失之前曾患有失眠症。此外,与健康受试者相比,SSNHL患者的PB白细胞中PER1,CRY1,CRY2,CLOCK,BMAL1和CKlε的表达显着降低。 SSNHL眩晕患者的CRY1和CKlε表达明显低于无眩晕症状的患者。我们的结果暗示了SSNHL中睡眠障碍和昼夜节律紊乱的相关性。

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