Department of Medical Biochemistry, Faculty of Medicine, Malatya Turgut Özal University, Malatya, Turkey.
Department of Pulmonary Medicine, Faculty of Medicine, Malatya Turgut Özal University, Malatya, Turkey.
Sleep Breath. 2024 Mar;28(1):151-163. doi: 10.1007/s11325-023-02870-9. Epub 2023 Jul 11.
Ischemia-modified albumin (IMA), total oxidant status (TOS), and total antioxidant status (TAS) are biomarkers used to evaluate oxidative stress status in various diseases including obstructive sleep apnea (OSA). In this study, we investigated the effects of disease severity and comorbidity on IMA, TOS and TAS levels in OSA.
Patients with severe OSA (no-comorbidity, one comorbidity, and multiple comorbidities) and mild-moderate OSA (no-comorbidity, one and multiple comorbidities), and healthy controls were included in the study. Polysomnography was applied to all cases and blood samples were taken from each participant at the same time of day. ELISA was used to measure IMA levels in serum samples and colorimetric commercial kits were used to perform TOS and TAS analyses. In addition, routine biochemical analyses were performed on all serum samples.
A total of 74 patients and 14 healthy controls were enrolled. There was no statistically significant difference between the disease groups according to gender, smoking status, age, body mass index (BMI), HDL, T3, T4, TSH, and B12 (p > 0.05). As the severity of OSA and comorbidities increased, IMA, TOS, apnea-hypopnea index (AHI), desaturation index (T90), cholesterol, LDL, triglyceride, AST, and CRP values increased significantly (p < 0.05). On the other hand, TAS, minimum desaturation, and mean desaturation values decreased significantly (p < 0.05).
We concluded that IMA, TOS, and TAS levels may indicate OSA-related oxidative stress, but as the severity of OSA increases and with the presence of comorbidity, IMA and TOS levels may increase and TAS levels decrease. These findings suggest that disease severity and presence/absence of comorbidity should be considered in studies on OSA.
缺血修饰白蛋白(IMA)、总氧化状态(TOS)和总抗氧化状态(TAS)是用于评估包括阻塞性睡眠呼吸暂停(OSA)在内的各种疾病中氧化应激状态的生物标志物。在这项研究中,我们研究了疾病严重程度和合并症对 OSA 患者 IMA、TOS 和 TAS 水平的影响。
本研究纳入了严重 OSA(无合并症、一种合并症和多种合并症)和轻中度 OSA(无合并症、一种和多种合并症)患者以及健康对照组。所有病例均进行多导睡眠图检查,并在同一天采集每位参与者的血液样本。酶联免疫吸附法(ELISA)用于检测血清样本中的 IMA 水平,比色商业试剂盒用于进行 TOS 和 TAS 分析。此外,对所有血清样本进行常规生化分析。
共纳入 74 例患者和 14 例健康对照者。根据性别、吸烟状况、年龄、体重指数(BMI)、高密度脂蛋白(HDL)、T3、T4、TSH 和 B12,疾病组之间无统计学差异(p>0.05)。随着 OSA 严重程度和合并症的增加,IMA、TOS、呼吸暂停低通气指数(AHI)、脱氧饱和度指数(T90)、胆固醇、低密度脂蛋白(LDL)、甘油三酯、天冬氨酸氨基转移酶(AST)和 C 反应蛋白(CRP)水平显著升高(p<0.05)。另一方面,TAS、最低脱氧饱和度和平均脱氧饱和度值显著降低(p<0.05)。
我们得出结论,IMA、TOS 和 TAS 水平可能表明与 OSA 相关的氧化应激,但随着 OSA 严重程度的增加以及合并症的存在,IMA 和 TOS 水平可能升高,而 TAS 水平可能降低。这些发现表明,在 OSA 研究中应考虑疾病严重程度和合并症的存在/缺失。