Respiratory Division & Sleep Laboratory, McGill University Health Centre, Montreal, QC, Canada; Respiratory & Epidemiology and Clinical Research Unit, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Meakins-Christie Laboratories, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Sleep Med. 2022 Feb;90:258-261. doi: 10.1016/j.sleep.2021.11.018. Epub 2022 Feb 12.
Obstructive sleep apnea (OSA) exacerbates Parkinson's disease (PD) manifestations including cognitive dysfunction. Both OSA and PD have been associated with inflammation. Brain-derived neurotrophic factor (BDNF) has been implicated in cognitive function. We aimed to investigate inflammatory cytokines and BDNF in relation to OSA and PD symptoms.
In a prospective observational study, patients with PD underwent overnight polysomnography. Morning serum levels of interleukin (IL)-1β, IL-6, IL-8, TNFα, and BDNF were quantified at baseline (n = 64) and 6 months (n = 38). Outcomes included non-motor and motor standard scores; Montreal Cognitive Assessment (MoCA); and Epworth Sleepiness scale (ESS). Associations were assessed using linear regression, adjusting for age, sex and body mass index.
At baseline, IL-6 was associated with the Apnea-Hypopnea Index (β = 0.013, p = 0.03), and the Oxygen Desaturation Index (β = 0.028, p = 0.002). No other associations between cytokines and sleep parameters were found. Motor dysfunction was associated with IL-6 (β = 0.03, p = 0.001). ESS was associated non-significantly with IL-6 (β = 0.04, p = 0.07) and BDNF (β = 555, p = 0.06). At follow-up, change in IL-6 was associated with change in non-motor (β = 0.08, p = 0.007), and motor (β = 0.03, p = 0.001) symptoms. Change in BDNF was associated with change in ESS (β = 1450, p = 0.02).
We found an association between IL-6 levels and both OSA severity and PD motor dysfunction. At follow-up, increasing IL-6 correlated with deterioration of motor and non-motor PD symptoms. Increasing BDNF correlated with increasing sleepiness. Further work with a larger sample size is needed, but our results support the hypothesis that OSA-related inflammation plays a role in PD manifestations and progression.
阻塞性睡眠呼吸暂停(OSA)可加重帕金森病(PD)的临床表现,包括认知功能障碍。OSA 和 PD 均与炎症有关。脑源性神经营养因子(BDNF)与认知功能有关。我们旨在研究与 OSA 和 PD 症状相关的炎症细胞因子和 BDNF。
在一项前瞻性观察性研究中,PD 患者接受了整夜多导睡眠图检查。在基线时(n=64)和 6 个月时(n=38)测量了早晨血清中白细胞介素(IL)-1β、IL-6、IL-8、TNFα 和 BDNF 的水平。结局包括非运动和运动标准评分;蒙特利尔认知评估(MoCA);和 Epworth 嗜睡量表(ESS)。使用线性回归,调整年龄、性别和体重指数,评估关联。
在基线时,IL-6 与呼吸暂停-低通气指数(β=0.013,p=0.03)和氧减指数(β=0.028,p=0.002)相关。在睡眠参数与细胞因子之间未发现其他关联。运动功能障碍与 IL-6 相关(β=0.03,p=0.001)。ESS 与 IL-6 (β=0.04,p=0.07)和 BDNF (β=555,p=0.06)呈非显著相关。在随访时,IL-6 的变化与非运动(β=0.08,p=0.007)和运动(β=0.03,p=0.001)症状的变化相关。BDNF 的变化与 ESS 的变化相关(β=1450,p=0.02)。
我们发现 IL-6 水平与 OSA 严重程度和 PD 运动功能障碍之间存在关联。在随访时,IL-6 的增加与 PD 运动和非运动症状的恶化相关。BDNF 的增加与嗜睡的增加相关。需要更大的样本量进行进一步研究,但我们的结果支持 OSA 相关炎症在 PD 表现和进展中起作用的假说。