Pilkauskaite Guoda, Miliauskas Skaidrius, Vitkauskiene Astra, Sakalauskas Raimundas
Department of Pulmonology and Immunology, Lithuanian University of Health Sciences, Eiveniu 2, 50009, Kaunas, Lithuania,
Sleep Breath. 2014 Dec;18(4):869-74. doi: 10.1007/s11325-014-0958-0. Epub 2014 Feb 25.
Mechanisms linking obstructive sleep apnea (OSA) to vascular diseases as well as obesity and metabolic syndrome are not clear. The purpose of the study was to evaluate levels of vascular adhesion molecules (soluble vascular cell adhesion molecules-1 (sVCAM-1) and E-selectin) in men with obstructive sleep apnea and control subjects and to determine their relations with obesity and metabolic syndrome.
Men with OSA and controls matched for age were included in the study. Overnight polysomnography was performed. Body mass index (BMI) and all the components of metabolic syndrome were evaluated. Serum levels of sVCAM-1 and E-selectin were measured by enzyme-linked immunosorbent assay. Data presented as median (25th and 75th percentiles).
Levels of sVCAM-1 (698.2 (627.6-798.2) vs 565.5 (518.8-678.1) ng/ml, p=0.003) and E-selectin (64.9 (50.1-83.1) vs 49.7 (39.8-59.5) ng/ml, p=0.017) were higher in the OSA group compared to the controls. Half of OSA patients had metabolic syndrome. Serum levels of sVCAM-1 and E-selectin did not differ in OSA patients with and without metabolic syndrome. Concentrations of both vascular adhesion molecules correlated with oxygen desaturation index (ODI), but the relation was no more significant after adjustment for all the components of metabolic syndrome. After adjustment for BMI, sVCAM-1 levels positively correlated with oxygen desaturation index (r=0.331, p=0.009).
Serum levels of sVCAM-1 and E-selectin were increased in the OSA patient group compared to the controls. sVCAM-1 showed relation with ODI after adjustment for BMI suggesting that it could contribute to development of cardiovascular consequences in OSA patients.
阻塞性睡眠呼吸暂停(OSA)与血管疾病以及肥胖和代谢综合征之间的联系机制尚不清楚。本研究的目的是评估阻塞性睡眠呼吸暂停男性患者和对照受试者的血管黏附分子(可溶性血管细胞黏附分子-1(sVCAM-1)和E-选择素)水平,并确定它们与肥胖和代谢综合征的关系。
本研究纳入了年龄匹配的阻塞性睡眠呼吸暂停男性患者和对照者。进行了整夜多导睡眠图检查。评估了体重指数(BMI)和代谢综合征的所有组成部分。通过酶联免疫吸附测定法测量血清sVCAM-1和E-选择素水平。数据以中位数(第25和第75百分位数)表示。
与对照组相比,阻塞性睡眠呼吸暂停组的sVCAM-1水平(698.2(627.6 - 798.2)对565.5(518.8 - 678.1)ng/ml,p = 0.003)和E-选择素水平(64.9(50.1 - 83.1)对49.7(39.8 - 59.5)ng/ml,p = 0.017)更高。一半的阻塞性睡眠呼吸暂停患者患有代谢综合征。有和没有代谢综合征的阻塞性睡眠呼吸暂停患者的血清sVCAM-1和E-选择素水平没有差异。两种血管黏附分子的浓度均与氧去饱和指数(ODI)相关,但在对代谢综合征的所有组成部分进行调整后,这种关系不再显著。在对BMI进行调整后,sVCAM-1水平与氧去饱和指数呈正相关(r = 0.331,p = 0.009)。
与对照组相比,阻塞性睡眠呼吸暂停患者组的血清sVCAM-1和E-选择素水平升高。在对BMI进行调整后,sVCAM-1与ODI显示出相关性,表明它可能有助于阻塞性睡眠呼吸暂停患者心血管后果的发展。