Department of Sleep Medicine and Metabolic Disorder, Medical University of Lodz, 6/8 Mazowiecka, 92-215 Lodz, Poland.
Department of Immunology and Allergy, Medical University of Lodz, 251 Pomorska, 92-213 Lodz, Poland.
Int J Mol Sci. 2024 Aug 2;25(15):8469. doi: 10.3390/ijms25158469.
Obstructive sleep apnea (OSA) has been linked to disruptions in circadian rhythm and neurotrophin (NFT) signaling. This study explored the link between neuromodulators, chronotype, and insomnia in OSA. The participants (n = 166) underwent polysomnography (PSG) before being categorized into either the control or the OSA group. The following questionnaires were completed: Insomnia Severity Index (ISI), Epworth Sleepiness Scale, Chronotype Questionnaire (morningness-eveningness (ME), and subjective amplitude (AM). Blood samples were collected post-PSG for protein level assessment using ELISA kits for brain-derived neurotrophic factor (BDNF), proBDNF, glial-cell-line-derived neurotrophic factor, NFT3, and NFT4. Gene expression was analyzed utilizing qRT-PCR. No significant differences were found in neuromodulator levels between OSA patients and controls. The controls with insomnia exhibited elevated neuromodulator gene expression ( < 0.05). In the non-insomnia individuals, BDNF and NTF3 expression was increased in the OSA group compared to controls ( = 0.007 for both); there were no significant differences between the insomnia groups. The ISI scores positively correlated with all gene expressions in both groups, except for NTF4 in OSA (R = 0.127, = 0.172). AM and ME were predicting factors for the ISI score and clinically significant insomnia ( < 0.05 for both groups). Compromised compensatory mechanisms in OSA may exacerbate insomnia. The correlation between chronotype and NFT expression highlights the role of circadian misalignments in sleep disruptions.
阻塞性睡眠呼吸暂停(OSA)与昼夜节律紊乱和神经营养因子(NFT)信号传导有关。本研究探讨了神经调节剂、昼夜型和 OSA 中失眠之间的联系。参与者(n=166)在进行多导睡眠图(PSG)检查之前,先被分为对照组或 OSA 组。完成以下问卷:失眠严重程度指数(ISI)、Epworth 嗜睡量表、昼夜类型问卷(晨型-晚型(ME)和主观振幅(AM)。PSG 后采集血样,使用 ELISA 试剂盒评估脑源性神经营养因子(BDNF)、proBDNF、胶质细胞源性神经营养因子、NFT3 和 NFT4 的蛋白水平。利用 qRT-PCR 分析基因表达。OSA 患者和对照组之间的神经调节剂水平没有差异。失眠对照组的神经调节剂基因表达升高(<0.05)。在非失眠个体中,与对照组相比,OSA 组的 BDNF 和 NTF3 表达增加(均为=0.007);两组之间没有显著差异。ISI 评分与两组中所有基因表达呈正相关,除了 OSA 中的 NTF4(R=0.127,=0.172)。AM 和 ME 是 ISI 评分和临床显著失眠的预测因素(两组均<0.05)。OSA 中代偿机制受损可能会加重失眠。昼夜型与 NFT 表达之间的相关性突出了昼夜节律失调在睡眠障碍中的作用。