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成年阻塞性睡眠呼吸暂停患者白细胞介素-35 和白细胞介素-37 水平升高。

Elevated levels of interleukin-35 and interleukin-37 in adult patients with obstructive sleep apnea.

机构信息

Department of Respiratory and Critical Care Medicine, Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.

出版信息

J Clin Lab Anal. 2021 Jun;35(6):e23790. doi: 10.1002/jcla.23790. Epub 2021 May 4.

DOI:10.1002/jcla.23790
PMID:33942365
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8183935/
Abstract

BACKGROUND

Systemic inflammation has a critical role in the pathogenesis of obstructive sleep apnea (OSA). Interleukin (IL)-35 and IL-37 have been identified as novel immune-modulating cytokines with anti-inflammatory activities in numerous types of inflammatory disease. The present study aimed to examine the serum levels of IL-35 and IL-37 in patients with OSA, and to investigate their associations with the severity of OSA.

METHODS

A total of 97 patients, including 67 cases of OSA and 30 age- and gender-matched healthy control subjects, were enrolled in the present study. All subjects were evaluated by overnight polysomnography. Serum IL-35, IL-37, and pro-inflammatory cytokine IL-1β levels were examined by ELISA.

RESULTS

Compared with those in the control subjects, serum IL-35, IL-37, and IL-1β levels were significantly elevated in patients with mild, moderate, or severe OSA. Furthermore, a severity-dependent increase in serum IL-35 and IL-37 levels was observed in patients with OSA. IL-35 and IL-37 levels were positively correlated with the apnea-hypopnea index (r = 0.742 and 0.578, respectively; both p < 0.001), while they were negatively correlated with the mean oxygen saturation (r = -0.461 and -0.339, respectively; both p < 0.001) and lowest oxyhaemoglobin saturation (r = -0.616 and -0.463, respectively; both p < 0.001) in patients with OSA. In addition, a positive correlation was observed between IL-35 or IL-37 and IL-1β levels (all p < 0.001).

CONCLUSION

The serum levels of IL-35 and IL-37 were significantly increased in patients with OSA and associated with the severity of OSA, implying that IL-35 and IL-37 may have a protective role in OSA by counteracting inflammatory responses.

摘要

背景

系统性炎症在阻塞性睡眠呼吸暂停(OSA)的发病机制中起着关键作用。白细胞介素(IL)-35 和 IL-37 已被确定为具有抗炎活性的新型免疫调节细胞因子,在多种炎症性疾病中具有抗炎作用。本研究旨在检测 OSA 患者血清中 IL-35 和 IL-37 的水平,并探讨其与 OSA 严重程度的关系。

方法

本研究共纳入 97 例患者,其中 67 例为 OSA 患者,30 例为年龄和性别匹配的健康对照者。所有受试者均行整夜多导睡眠图检查。采用 ELISA 法检测血清 IL-35、IL-37 和促炎细胞因子 IL-1β 水平。

结果

与对照组相比,轻度、中度和重度 OSA 患者的血清 IL-35、IL-37 和 IL-1β 水平均显著升高。此外,OSA 患者的血清 IL-35 和 IL-37 水平呈与严重程度相关的升高趋势。IL-35 和 IL-37 水平与呼吸暂停低通气指数呈正相关(r 分别为 0.742 和 0.578,均 P<0.001),与平均血氧饱和度呈负相关(r 分别为-0.461 和-0.339,均 P<0.001),与最低血氧饱和度呈负相关(r 分别为-0.616 和-0.463,均 P<0.001)。此外,IL-35 或 IL-37 与 IL-1β 水平呈正相关(均 P<0.001)。

结论

OSA 患者血清 IL-35 和 IL-37 水平显著升高,并与 OSA 的严重程度相关,表明 IL-35 和 IL-37 可能通过拮抗炎症反应在 OSA 中发挥保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8183935/428d2682fbeb/JCLA-35-e23790-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8183935/5eea901ee08d/JCLA-35-e23790-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8183935/3b6f95e9bedc/JCLA-35-e23790-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8183935/428d2682fbeb/JCLA-35-e23790-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8183935/5eea901ee08d/JCLA-35-e23790-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8183935/3b6f95e9bedc/JCLA-35-e23790-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8183935/428d2682fbeb/JCLA-35-e23790-g002.jpg

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