Department of Psychiatry, Faculty of Medicine, University of Debrecen, Nagyerdei krt. 98, Debrecen, 4032, Hungary.
Department of Health Systems Management and Quality Management for Health Care, Faculty of Public Health, University of Debrecen, Nagyerdei krt. 98, Debrecen, 4032, Hungary.
Respir Res. 2019 Apr 5;20(1):67. doi: 10.1186/s12931-019-1033-y.
Obstructive sleep apnea hypopnea syndrome (OSAHS) is a sleep-related breathing disorder, characterized by excessive daytime sleepiness (EDS), paralleled by intermittent collapse of the upper airway. EDS may be the symptom of OSAHS per se but may also be due to the alteration of central circadian regulation. Irisin is a putative myokine and has been shown to induce BDNF expression in several sites of the brain. BDNF is a key factor regulating photic entrainment and consequent circadian alignment and adaptation to the environment. Therefore, we hypothesized that EDS accompanying OSAHS is reflected by alteration of irisin/BDNF axis.
Case history, routine laboratory parameters, serum irisin and BDNF levels, polysomnographic measures and Epworth Sleepiness Scale questionnaire (ESS) were performed in a cohort of OSAHS patients (n = 69). Simple and then multiple linear regression was used to evaluate data.
We found that EDS reflected by the ESS is associated with higher serum irisin and BDNF levels; β: 1.53; CI: 0.35, 6.15; p = 0.012 and β: 0.014; CI: 0.0.005, 0.023; p = 0.02, respectively. Furthermore, influence of irisin and BDNF was significant even if the model accounted for their interaction (p = 0.006 for the terms serum irisin, serum BDNF and their interaction). Furthermore, a concentration-dependent effect of both serum irisin and BDNF was evidenced with respect to their influence on the ESS.
These results suggest that the irisin-BDNF axis influences subjective daytime sleepiness in OSAS patients reflected by the ESS. These results further imply the possible disruption of the circadian regulation in OSAHS. Future interventional studies are needed to confirm this observation.
阻塞性睡眠呼吸暂停低通气综合征(OSAHS)是一种与睡眠相关的呼吸障碍,其特征是白天过度嗜睡(EDS),同时上气道间歇性塌陷。EDS 可能是 OSAHS 本身的症状,也可能是由于中枢昼夜节律调节的改变。鸢尾素是一种假定的肌因子,已被证明可在大脑的多个部位诱导 BDNF 表达。BDNF 是调节光刺激同步和随后昼夜节律对齐以及适应环境的关键因素。因此,我们假设伴随 OSAHS 的 EDS 反映了鸢尾素/BDNF 轴的改变。
对一组 OSAHS 患者(n=69)进行了病史、常规实验室参数、血清鸢尾素和 BDNF 水平、多导睡眠图测量和 Epworth 嗜睡量表问卷(ESS)。采用简单和多元线性回归分析来评估数据。
我们发现 ESS 反映的 EDS 与较高的血清鸢尾素和 BDNF 水平相关;β:1.53;CI:0.35,6.15;p=0.012 和β:0.014;CI:0.005,0.023;p=0.02,分别。此外,即使模型考虑了它们的相互作用,鸢尾素和 BDNF 的影响仍然显著(血清鸢尾素、血清 BDNF 及其相互作用项的 p 值分别为 0.006)。此外,还证明了血清鸢尾素和 BDNF 对 ESS 的影响存在浓度依赖性。
这些结果表明,鸢尾素-BDNF 轴影响 OSA 患者 ESS 反映的日间嗜睡。这些结果进一步表明,OSAHS 可能破坏了昼夜节律调节。需要进一步的干预研究来证实这一观察结果。