Yang Hyunju, Engeland Christopher G, King Tonya S, Sawyer Amy M
Chonnam National University, College of Nursing, Gwangju, South Korea.
The Pennsylvania State University, Department of Biobehavioral Health, University Park, Pennsylvania.
J Clin Sleep Med. 2020 May 15;16(5):715-723. doi: 10.5664/jcsm.8332. Epub 2020 Feb 7.
To identify the relationship between (1) cytokines and everyday symptoms and (2) cytokine diurnal variation and everyday symptoms in mild obstructive sleep apnea (OSA).
An observational, single-night study of 20 adults with mild to moderate OSA undergoing diagnostic polysomnography. Everyday symptoms included sleepiness measured by Stanford Sleepiness Scale, fatigue and energy levels measured by Lee Fatigue Scale, and cytokine plasma concentrations including interleukin (IL)-1β, IL-6, IL-8, and tumor necrosis factor-α (TNF-α) measured concurrent with symptoms at presleep (8 pm to 10 pm; time 1) and postsleep (5 am to 6 am; time. 2) Cytokine diurnal variation was calculated as [time 2 - time 1]. Wilcoxon signed-rank tests and Spearman partial rank correlations adjusted for age, body mass index, cardiovascular disease, and type 2 diabetes were used.
Twenty patients (50% male, obese, median age = 51.0 years) with mild OSA (apnea-hypopnea index, AHI; median 9.5 events/h) were evaluated. Evening IL-6 was associated with evening symptoms, including sleepiness (r = .69, P = .002) and energy level (r = -0.68, P = .003); morning IL-8 (r = .73, P = .001), and TNF-α (r = .59, P = .015) were associated with morning fatigue. Only morning IL-8 (r = -0.57, P = .022) and diurnal variations in IL-8 (r = -0.60, P = .014) were associated with morning energy level.
There is scant evidence addressing the diurnal variation of inflammatory biomarkers and the relationship with symptom expression in mild OSA. The present findings provide preliminary mechanistic findings for symptom expression in OSA and contribute insight to mild OSA symptom phenotypes.
确定(1)细胞因子与日常症状之间的关系,以及(2)轻度阻塞性睡眠呼吸暂停(OSA)患者细胞因子的昼夜变化与日常症状之间的关系。
对20名患有轻度至中度OSA的成年人进行一项观察性单夜研究,这些患者均接受了诊断性多导睡眠监测。日常症状包括用斯坦福嗜睡量表测量的嗜睡程度、用李氏疲劳量表测量的疲劳和精力水平,以及细胞因子血浆浓度,包括白细胞介素(IL)-1β、IL-6、IL-8和肿瘤坏死因子-α(TNF-α),这些细胞因子在睡前(晚上8点至10点;时间1)和睡眠后(早上5点至6点;时间2)与症状同时测量。细胞因子的昼夜变化计算为[时间2 - 时间1]。使用了经年龄、体重指数、心血管疾病和2型糖尿病校正的Wilcoxon符号秩检验和Spearman偏秩相关分析。
对20例轻度OSA患者(50%为男性,肥胖,中位年龄 = 51.0岁)进行了评估,其呼吸暂停低通气指数(AHI)中位值为9.5次/小时。晚上的IL-6与晚上的症状相关,包括嗜睡(r = 0.69,P = 0.002)和精力水平(r = -0.68,P = 0.003);早上的IL-8(r = 0.73,P = 0.001)和TNF-α(r = 0.59,P = 0.015)与早上的疲劳相关。只有早上的IL-8(r = -0.57,P = 0.022)和IL-8的昼夜变化(r = -0.60,P = 0.014)与早上的精力水平相关。
关于轻度OSA中炎症生物标志物的昼夜变化及其与症状表达之间的关系,现有证据很少。本研究结果为OSA症状表达提供了初步的机制性发现,并有助于深入了解轻度OSA症状表型。