Phillips Bradley G, Wang Ye, Ambati Suresh, Ma Ping, Meagher Richard B
Clinical and Administrative Pharmacy, University of Georgia, Athens, GA 30602, USA; Clinical and Translational Research Unit, University of Georgia, Athens, GA 30602, USA.
Department of Statistics, University of Georgia, Athens, GA 30602, USA.
Clin Immunol. 2020 Dec;221:108601. doi: 10.1016/j.clim.2020.108601. Epub 2020 Oct 2.
Obstructive Sleep Apnea (OSA) damages the health of 35% of adult Americans. Disordered sleep results in increased risk of several autoimmune disorders, but the molecular links to autoimmunity are poorly understood. Herein, we identified four cytokines associated with autoimmune disease, whose median serum levels were significantly different for OSA patients receiving airways therapy, from the levels in untreated OSA patients, APRIL (5.2-fold lower, p = 3.5 × 10), CD30 (1.6-fold higher, p = 7.7 × 10), IFN-Alpha-2 (2.9-fold higher, p = 9.6 × 10) and IL-2 (1.9-fold higher, p = 0.0003). Cytokine levels in airways treated patients were similar to the levels in control subjects. t-SNE and UMAP analysis of these high dimensional patient cytokine data identified only two groups, suggesting a similar global response for all four cytokines to airways therapy. Our findings suggest the levels of these four cytokines may be altered by disordered sleep and perhaps by chronic hypoxia. Therapeutic options are discussed.
阻塞性睡眠呼吸暂停(OSA)损害了35%的成年美国人的健康。睡眠紊乱会增加多种自身免疫性疾病的风险,但与自身免疫的分子联系却知之甚少。在此,我们鉴定出四种与自身免疫性疾病相关的细胞因子,接受气道治疗的OSA患者的血清水平中位数与未经治疗的OSA患者相比有显著差异,分别是增殖诱导配体(APRIL,降低5.2倍,p = 3.5×10)、CD30(升高1.6倍,p = 7.7×10)、干扰素α-2(升高2.9倍,p = 9.6×10)和白细胞介素-2(升高1.9倍,p = 0.0003)。接受气道治疗患者的细胞因子水平与对照组相似。对这些高维患者细胞因子数据进行t-SNE和UMAP分析仅识别出两组,表明所有四种细胞因子对气道治疗的整体反应相似。我们的研究结果表明,这四种细胞因子的水平可能因睡眠紊乱以及可能因慢性缺氧而改变。文中还讨论了治疗选择。