Feres Marcia C, Cintra Fatima D, Rizzi Camila F, Mello-Fujita Luciane, Lino de Souza Altay A, Tufik Sergio, Poyares Dalva
Psychobiology Department of Universidade Federal de São Paulo, Sao Paulo, SP, Brazil.
Cardiology Department of Universidade Federal de São Paulo, São Paulo, SP, Brazil.
PLoS One. 2014 Jun 9;9(6):e98407. doi: 10.1371/journal.pone.0098407. eCollection 2014.
Measurements of plasma and urinary catecholamine are susceptible to confounding factors that influence the results, complicating the interpretation of sympathetic nervous system (SNS) activity in the Obstructive sleep apnea (OSA) and arterial hypertension (HYP) conditions.
In this study, we validated a test for platelet catecholamine and compared the catecholamine levels (adrenaline and noradrenaline) in urine, plasma and platelets in patients with OSA and HYP compared with controls.
In the validation, 30 healthy, nonsmoking volunteers who were not currently undergoing treatment or medication were selected as the control group. One hundred fifty-four individuals (114 OSA, 40 non-OSA) were consecutively selected from the outpatient clinic of the Sleep Institute and underwent clinical, polysomnographic and laboratory evaluation, including the urinary, plasma and platelet levels of adrenaline (AD) and noradrenaline (NA). Patients were then allocated to groups according to the presence of OSA and/or hypertension.
A logistic regression model, controlled for age and BMI, showed that urinary AD and urinary NA were risk factors in the OSA+HYP group and the HYP group; however, the model showed higher levels of platelet NA for OSA without HYP. After 1 year of CPAP (continuous upper airway pressure) treatment, patients (n = 9) presented lower levels of urinary NA (p = 0.04) and platelet NA (p = 0.05).
Urinary NA and AD levels were significantly associated with the condition of hypertension with and without OSA, whereas platelet NA with OSA without comorbidity. These findings suggest that platelet catecholamine levels might reflect nocturnal sympathetic activation in OSA patients without hypertension.
血浆和尿儿茶酚胺的测量易受影响结果的混杂因素干扰,这使得在阻塞性睡眠呼吸暂停(OSA)和动脉高血压(HYP)情况下对交感神经系统(SNS)活动的解读变得复杂。
在本研究中,我们验证了一项血小板儿茶酚胺检测,并比较了OSA和HYP患者与对照组尿液、血浆和血小板中的儿茶酚胺水平(肾上腺素和去甲肾上腺素)。
在验证过程中,选择30名未接受治疗或用药的健康非吸烟志愿者作为对照组。从睡眠研究所门诊连续选取154名个体(114名OSA患者,40名非OSA患者),并进行临床、多导睡眠图和实验室评估,包括尿液、血浆和血小板中肾上腺素(AD)和去甲肾上腺素(NA)的水平。然后根据是否存在OSA和/或高血压将患者分组。
在控制年龄和BMI的逻辑回归模型中,显示尿AD和尿NA是OSA + HYP组和HYP组的危险因素;然而,该模型显示无HYP的OSA患者血小板NA水平更高。在持续气道正压通气(CPAP)治疗1年后,患者(n = 9)的尿NA水平(p = 0.04)和血小板NA水平(p = 0.05)降低。
尿NA和AD水平与伴或不伴OSA的高血压状况显著相关,而血小板NA与无合并症的OSA相关。这些发现表明血小板儿茶酚胺水平可能反映无高血压的OSA患者的夜间交感神经激活。