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OSAHS患者血清可溶性髓样细胞触发受体2水平的变化及其意义
作者:阚海峰  马兰玉  陈龙 
单位:如皋市人民医院 呼吸与危重症医学科, 江苏 南通 226500
关键词:阻塞性睡眠呼吸暂停低通气综合征 可溶性髓样细胞触发受体2 认知功能障碍 
分类号:R563.9
出版年·卷·期(页码):2023·51·第十期(1423-1427)
摘要:

目的:检测阻塞性睡眠呼吸暂停低通气综合征(OSAHS)患者血清可溶性髓样细胞触发受体2(sTREM2)水平并探讨其临床意义。方法:选取在我院门诊和住院接受多导睡眠(PSG)监测的人群作为受试者,根据睡眠呼吸暂停低通气指数(AHI)将受试者分为OSAHS组61例(AHI≥5次·h-1)和对照组30例(AHI<5次·h-1)。根据蒙特利尔认知评估(MoCA)将OSAHS组分成认知功能正常(MoCA得分≥26分,41例)和合并轻度认知功能障碍(MCI)(MoCA得分<26分,20例)。采用ELISA法测定所有受试者的血清sTREM2的含量。结果:OSAHS组患者的血清sTREM2水平较对照组升高(P<0.05),且与认知功能正常的OSAHS患者相比,合并MCI的OSAHS患者血清sTREM2水平更高(P<0.05)。OSAHS患者的sTREM2水平受MoCA评分、平均血氧饱和度(MSaO2)和血氧饱和度低于90%的时间占总监测时间的百分比(TS90%)的影响,MoCA评分、MSaO2较低且TS90%较高的OSAHS患者血清sTEM2水平可能更高。结论:OSAHS患者血清sTREM2水平升高,尤其是合并MCI的患者。因此,血清sTREM2水平有可能成为OSAHS患者MCI的生物标志物。

Objective: This study aimed to compare serum levels of soluble triggering receptor expresses on myeloid cells 2(sTREM2) in normal individuals and patients with obstructive sleep apnea-hypopnea syndrome(OSAHS). Methods: People who received polysomnography(PSG) monitoring in our hospital were selected as subjects. According to the sleep apnea-hypopnea index(AHI), the subjects were divided into OSAHS group(AHI ≥ 5 times·h-1,n=61) and control group(AHI<5 times·h-1, n=30). According to the Montreal cognitive assessment(MoCA) score,the patients of OSAHS group were divided into the normal cognitive function(MoCA ≥ 26 points, n=41) and the mild cognitive impairment(MCI)(MoCA<26 points,n=20). The serum STREM2 content was determined by ELISA in all subjects. Results: OSAHS group had higher serum sTREM2 levels than the control group(P<0.05). Additionally, serum sTREM2 levels were higher in OSAHS patients with MCI(P<0.05). Multivariate linear regression analysis showed that serum sTREM2 levels in patients with OSAHS were associated with the MoCA score, MSaO2 and TS90% levels. OSAHS Patients with low MoCA scores, low MSaO2, and higher TS90% may have higher serum sTEM2 levels. Conclusion: Serum sTREM2 levels are elevated in patients with OSAHS, especially those with MCI. Therefore, serum sTREM2 levels have the potential to become biomarker of MCI in OSAHS patients.

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