Sex-specific impact of obstructive sleep apnea on peripheral blood mononuclear cells.

IF 2.1 4区 医学 Q3 CLINICAL NEUROLOGY
Joshua M Bock, Soumya Vungarala, Sreeja Sompalli, Prachi Singh, Kevin D Pavelko, Richard B Kennedy, Virend K Somers
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引用次数: 0

Abstract

Purpose: Experimental sleep disruption in healthy adults is more deleterious to immune function in females relative to males; however, it remains unknown if this translates to patients with obstructive sleep apnea (OSA). Thus, this study explored sex differences in peripheral blood mononuclear cells (PBMCs) from patients with untreated OSA.

Methods: Participants completed sleep studies to identify the presence of OSA via the apnea-hypopnea index (AHI). PBMCs were isolated, cryopreserved, and batch phenotyped via mass cytometry.

Results: Females with (n = 6, AHI = 25.9 ± 21.4 events/hr, age = 37 ± 14yrs, BMI = 30.5 ± 7.4 kg/m2) and without (n = 9, AHI = 2.6 ± 1.6 events/hr, age = 35 ± 10yrs, BMI = 29.2 ± 6.3 kg/m2) OSA were compared to males with (n = 7, AHI = 13.7 ± 8.5 events/hr, age = 33 ± 11yrs, BMI = 30.0 ± 4.8 kg/m2) and without (n = 7, AHI = 2.6 ± 1.6 events/hr, age = 33 ± 10yrs, BMI = 28.9 ± 3.8 kg/m2) OSA. No significant group-by-sex interactions were observed in CD3 T cells (p = 0.273), CD8 T cells (p = 0.656), B cells (p = 0.190), monocytes (p = 0.638), nor granulocytes (p = 0.267) expressed as a percent of their respective parent population. While the percentage of total NK cells did not differ between groups (group-by-sex p = 0.822), females with OSA had fewer CD57- (42.4 ± 14.7 vs. 62.4 ± 10.4%) and more CD57+ (57.6 ± 14.7 vs. 37.6 ± 10.4%) NK cells than females without OSA (p < 0.050). No differences in CD57- (53.6 ± 18.1 vs. 44.9 ± 16.8%) and CD57+ (46.4 ± 18.1 vs. 55.2 ± 19.8%) NK cells were observed between males (p = 0.283). Tregs were more prevalent in females with vs. females without OSA (2.17 ± 0.64 vs. 1.31 ± 0.41%, p = 0.006) with no difference between males (1.55 ± 0.50 vs. 1.71 ± 0.71%, p = 0.601).

Conclusions: Our data suggest that OSA increases the prevalence of cytotoxic NK cells and Tregs in females. The causes and downstream effects of these changes remain undetermined.

阻塞性睡眠呼吸暂停对外周血单核细胞的性别特异性影响。
目的:健康成人实验性睡眠中断对女性免疫功能的损害大于男性;然而,尚不清楚这是否适用于阻塞性睡眠呼吸暂停(OSA)患者。因此,本研究探讨了未经治疗的OSA患者外周血单个核细胞(PBMCs)的性别差异。方法:参与者完成睡眠研究,通过呼吸暂停低通气指数(AHI)确定OSA的存在。分离pbmc,冷冻保存,并通过细胞计数进行批量表型分析。结果:女性(n = 6, AHI = 25.9±21.4事件/人力资源年龄= 37±14岁,体重指数= 30.5±7.4 kg / m2)没有(n = 9, AHI = 2.6±1.6事件/小时,35岁=±10岁,体重指数= 29.2±6.3 kg / m2)相较于男性阻塞性睡眠呼吸暂停综合症是与(n = 7, AHI = 13.7±8.5事件/人力资源年龄= 33±11岁,体重指数= 30.0±4.8 kg / m2)没有(n = 7, AHI = 2.6±1.6事件/人力资源年龄= 33±10岁,体重指数= 28.9±3.8 kg / m2)阻塞性睡眠呼吸暂停综合症。在CD3 T细胞(p = 0.273)、CD8 T细胞(p = 0.656)、B细胞(p = 0.190)、单核细胞(p = 0.638)和粒细胞(p = 0.267)在各自亲本群体中表达的百分比中,没有观察到显著的群体性别相互作用。两组间NK细胞总数无显著性差异(p = 0.822),但OSA女性的CD57-(42.4±14.7比62.4±10.4%)和CD57+(57.6±14.7比37.6±10.4%)NK细胞数量明显少于非OSA女性(p = 0.283) (p -(53.6±18.1比44.9±16.8%)和CD57+(46.4±18.1比55.2±19.8%)NK细胞。Tregs在有OSA的女性中比无OSA的女性更普遍(2.17±0.64比1.31±0.41%,p = 0.006),而在男性中无差异(1.55±0.50比1.71±0.71%,p = 0.601)。结论:我们的数据表明,OSA增加了女性细胞毒性NK细胞和Tregs的患病率。这些变化的原因和下游影响仍未确定。
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来源期刊
Sleep and Breathing
Sleep and Breathing 医学-呼吸系统
CiteScore
5.20
自引率
4.00%
发文量
222
审稿时长
3-8 weeks
期刊介绍: The journal Sleep and Breathing aims to reflect the state of the art in the international science and practice of sleep medicine. The journal is based on the recognition that management of sleep disorders requires a multi-disciplinary approach and diverse perspectives. The initial focus of Sleep and Breathing is on timely and original studies that collect, intervene, or otherwise inform all clinicians and scientists in medicine, dentistry and oral surgery, otolaryngology, and epidemiology on the management of the upper airway during sleep. Furthermore, Sleep and Breathing endeavors to bring readers cutting edge information about all evolving aspects of common sleep disorders or disruptions, such as insomnia and shift work. The journal includes not only patient studies, but also studies that emphasize the principles of physiology and pathophysiology or illustrate potentially novel approaches to diagnosis and treatment. In addition, the journal features articles that describe patient-oriented and cost-benefit health outcomes research. Thus, with peer review by an international Editorial Board and prompt English-language publication, Sleep and Breathing provides rapid dissemination of clinical and clinically related scientific information. But it also does more: it is dedicated to making the most important developments in sleep disordered breathing easily accessible to clinicians who are treating sleep apnea by presenting well-chosen, well-written, and highly organized information that is useful for patient care.
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