Sonka Karel, Kelemen Jano, Kemlink David, Volná Jana, Pretl Martin, Zima Tomas, Benakova Hana, Rambousek Petr, Foltán René, Donev Filip
Department of Neurology, 1st Medical Faculty and General Teaching Hospital, Charles University, Prague, Czech Republic.
Neuro Endocrinol Lett. 2007 Oct;28(5):575-9.
Responsible for sleep brain perfusion changes, obstructive sleep apnea (OSA) constitutes a cardiovascular risk. To find out about any diffuse damage to the brain tissue, we studied the S100B protein, whose serum level is known to rise in stroke and craniocerebral trauma.
60 men (mean age 51.7+/-11.8 years) referred to us for OSA without any major comorbidity were examined polygraphically. S100B was determined with electrochemiluminiscence immunoassay (ECLIA) from evening and morning blood samples.
All sixty men were diagnosed with OSA. The difference between the evening level of S100B 0.068+/-0.030 microg/l and the morning level 0.059+/-0.029 microg/l was significant (p=0.0004). Patients with mild OSA were found to have the evening S100B 0.063+/-0.023 microg/l, the morning level 0.042+/-0.012 microg/l, the difference being significant (p=0.00051). In moderate OSA the difference between the evening -0.070+/-0.017 microg/l and morning levels -0.055+/-0.025 microg/l was less significant (p=0.043). In severe OSA no difference was found between the evening and morning concentrations of S100B (0.070+/-0.036 microg/l and 0.070+/-0.031 microg/l respectively). The difference between the evening and morning S100B levels correlated negatively with AHI and ODI and positively with basal saturation and average minimal oxygen saturation.
Sleep with signs of severe OSA influences S100B protein release.
阻塞性睡眠呼吸暂停(OSA)会导致睡眠时脑灌注改变,构成心血管风险。为了查明脑组织是否存在任何弥漫性损伤,我们研究了S100B蛋白,已知其血清水平在中风和颅脑创伤时会升高。
对60名因OSA前来就诊且无任何重大合并症的男性(平均年龄51.7±11.8岁)进行了多导睡眠监测。通过电化学发光免疫分析(ECLIA)测定傍晚和早晨血样中的S100B。
所有60名男性均被诊断为OSA。傍晚S100B水平0.068±0.030微克/升与早晨水平0.059±0.029微克/升之间的差异具有显著性(p = 0.0004)。轻度OSA患者傍晚S100B水平为0.063±0.023微克/升,早晨水平为0.042±0.012微克/升,差异具有显著性(p = 0.00051)。中度OSA患者傍晚水平-0.070±0.017微克/升与早晨水平-0.055±0.025微克/升之间的差异不太显著(p = 0.043)。重度OSA患者傍晚和早晨S100B浓度之间未发现差异(分别为0.用傍晚和早晨S100B水平之间的差异与呼吸暂停低通气指数(AHI)和氧减指数(ODI)呈负相关,与基础饱和度和平均最低氧饱和度呈正相关。
伴有重度OSA体征的睡眠会影响S100B蛋白的释放。