Pejovic Slobodanka, Shang Yimeng, Vgontzas Alexandros N, Fernandez-Mendoza Julio, He Fan, Li Yun, Kong Lan
Sleep Research & Treatment Center, Penn State Health Milton S. Hershey Medical Center, Pennsylvania State University, College of Medicine, Hershey, Pennsylvania, USA.
Department of Public Health Sciences, Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA.
J Sleep Res. 2025 Jun;34(3):e14386. doi: 10.1111/jsr.14386. Epub 2024 Oct 26.
C-reactive protein (CRP) appears to improve the ability to detect cardiometabolic risk in young and middle-aged adults with mild-to-moderate obstructive sleep apnea (mmOSA). The aim of this study is to assess utility of CRP in identifying the risk of hypertension and insulin resistance across a wide age range including older patients with mmOSA. Adults (n = 216) of a wide age range (28-90 years old, mean age 52.64 ± 12.74) with mmOSA (5 ≤ AHI < 30) completed in-lab polysomnography or home sleep apnea testing, physical examination including blood pressure (BP) measures, structured medical history questionnaire, and blood draw for CRP and fasting glucose and insulin levels. In adults < 60 years, lnCRP but not the apnea-hypopnea index (AHI) was associated with greater odds for hypertension (odds ratio [OR] = 2.40, 95% CI = 1.20-4.84, p = 0.01; OR = 1.00, 95% CI = 0.92-1.08, p = 0.92, respectively) and with higher average systolic and diastolic BP. Also, in adults < 60 years lnCRP but not AHI, was associated with higher lnHOMA values. In contrast, in adults > 60 years neither lnCRP nor AHI were associated with greater odds for hypertension, average systolic and diastolic BP, and lnHOMA. Receiver-operating characteristics curves revealed that adding CRP to standard clinical factors (age, sex, and BMI) yielded moderately good risk models for hypertension in patients < 60 years (AUC = 0.721). In conclusion, CRP improves the ability to detect cardiometabolic risk in young and middle-aged, but not older adults with mmOSA, suggesting that inflammation may be a primary pathogenetic mechanism in younger patients with OSA.
C反应蛋白(CRP)似乎能提高在患有轻至中度阻塞性睡眠呼吸暂停(mmOSA)的中青年成年人中检测心脏代谢风险的能力。本研究的目的是评估CRP在包括老年mmOSA患者在内的广泛年龄范围内识别高血压和胰岛素抵抗风险的效用。年龄范围广泛(28 - 90岁,平均年龄52.64±12.74)的mmOSA患者(5≤呼吸暂停低通气指数[AHI]<30,n = 216)完成了实验室多导睡眠图或家庭睡眠呼吸暂停测试、包括血压(BP)测量的体格检查、结构化病史问卷,并抽取血液检测CRP、空腹血糖和胰岛素水平。在60岁以下的成年人中,lnCRP而非呼吸暂停低通气指数(AHI)与高血压的更高几率相关(优势比[OR]=2.40,95%置信区间[CI]=1.20 - 4.84,p = 0.01;OR = 1.00,95% CI = 0.92 - 1.08,p = 0.92),且与更高的平均收缩压和舒张压相关。此外,在60岁以下的成年人中,lnCRP而非AHI与更高的胰岛素抵抗稳态模型评估(HOMA)值相关。相比之下,在60岁以上的成年人中,lnCRP和AHI均与高血压、平均收缩压和舒张压以及lnHOMA的更高几率无关。受试者工作特征曲线显示,在标准临床因素(年龄、性别和体重指数)中加入CRP,对于60岁以下患者的高血压产生了中度良好的风险模型(曲线下面积[AUC]=0.721)。总之,CRP提高了在患有mmOSA的中青年而非老年成年人中检测心脏代谢风险的能力,这表明炎症可能是年轻OSA患者的主要发病机制。