Peres Bernardo U, Allen A J Hirsch, Shah Aditi, Fox Nurit, Laher Ismail, Almeida Fernanda, Jen Rachel, Ayas Najib
Department of Oral Health Sciences, Faculty of Dentistry, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.
Department of Medicine, Faculty of Medicine, University of British Columbia, Vancouver, BC V6T 2B5, Canada.
Antioxidants (Basel). 2020 Jun 2;9(6):476. doi: 10.3390/antiox9060476.
Oxidative stress (OS) drives cardiometabolic diseases. Intermittent hypoxia consistently increases oxidative stress markers. Obstructive sleep apnea (OSA) patients experience intermittent hypoxia and an increased rate of cardiovascular disease, however, the impact of OSA on OS markers is not clear. The objective was to assess relationships between OSA severity and biomarker levels. Patients with suspected OSA referred for a polysomnogram (PSG) provided fasting blood sample. Plasma levels of 8-isoprostane, 8-hydroxydeoxyguanosine (8-OHdG), and superoxide dismutase (SOD) were measured. The relationship between OSA and OS was assessed both before and after controlling for confounders (age, sex, smoking history, history of cardiovascular disease, ethnicity, diabetes, statin usage, body mass index (BMI)). 402 patients were studied (68% male, mean age ± SD = 50.8 ± 11.8 years, apnea-hypopnea index (AHI) = 22.2 ± 21.6 events/hour, BMI = 31.62 ± 6.49 kg/m. In a multivariable regression, the AHI significantly predicted 8-isoprostane levels ( = 0.0008) together with age and statin usage; AHI was not a predictor of 8-OHdG or SOD. Female sex ( < 0.0001) and no previous history of cardiovascular disease ( = 0.002) were associated with increased antioxidant capacity. Circulating 8-isoprostane levels may be a promising biomarker of the severity of oxidative stress in OSA patients. Prospective studies are needed to determine whether this biomarker is associated with long-term cardiometabolic complications in OSA.
氧化应激(OS)会引发心脏代谢疾病。间歇性缺氧会持续增加氧化应激标志物。阻塞性睡眠呼吸暂停(OSA)患者会经历间歇性缺氧,且心血管疾病发病率增加,然而,OSA对氧化应激标志物的影响尚不清楚。目的是评估OSA严重程度与生物标志物水平之间的关系。因疑似OSA而接受多导睡眠图(PSG)检查的患者提供了空腹血样。检测了血浆中8-异前列腺素、8-羟基脱氧鸟苷(8-OHdG)和超氧化物歧化酶(SOD)的水平。在控制混杂因素(年龄、性别、吸烟史、心血管疾病史、种族、糖尿病、他汀类药物使用情况、体重指数(BMI))前后,评估了OSA与氧化应激之间的关系。对402名患者进行了研究(男性占68%,平均年龄±标准差 = 50.8 ± 11.8岁,呼吸暂停低通气指数(AHI) = 22.2 ± 21.6次/小时,BMI = 31.62 ± 6.49 kg/m²)。在多变量回归分析中,AHI与年龄和他汀类药物使用情况一起显著预测了8-异前列腺素水平(P = 0.0008);AHI不是8-OHdG或SOD的预测指标。女性(P < 0.0001)和既往无心血管疾病史(P = 0.002)与抗氧化能力增强有关。循环8-异前列腺素水平可能是OSA患者氧化应激严重程度的一个有前景的生物标志物。需要进行前瞻性研究来确定该生物标志物是否与OSA患者的长期心脏代谢并发症有关。