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作 者:李艳[1] 聂秀红[1] 张威[1] 樊晓军[1] 任魁[1] 高赏[1]
机构地区:[1]首都医科大学宣武医院呼吸科,北京100053
出 处:《中华全科医师杂志》2013年第10期816-819,共4页Chinese Journal of General Practitioners
摘 要:目的 探讨不同程度阻塞性睡眠呼吸暂停低通气综合征(OSAHS)患者体内植物凝集素样氧化低密度脂蛋白受体-1(LOX-1)及血脂的水平.方法 对2011年1月-7月间具有睡眠障碍症状的门诊患者94例进行多导睡眠图(PSG)监测,根据睡眠呼吸暂停低通气指数(AHI)分为3组,轻中度OSAHS组(5次/h≤AHI≤30次/h)27例,重度OSAHS组(AHI> 30次/h)37例,正常对照组(AHI<5次/h)30例,均检测血清LOX-1、TG、TC、HDL-C、LDL-C.结果 重度OSAHS组血清LOX-1水平最高,轻中度组、正常对照组依次减低,差异有统计学意义(P<0.01).OSAHS患者血清LOX-1水平与AHI、夜间最长呼吸暂停时间(LAT)呈正相关(r值分别为0.645、0.501,P<0.01),与夜间最低血氧饱和度(SaO2)呈负相关(r=-0.647,P<0.01).OSAHS组患者血脂水平与正常对照组差异无统计学意义(P>0.05).结论 OSAHS所造成的夜间间歇缺氧可导致血清LOX-1水平升高,血脂水平不能有效预测OSAHS患者脂代谢紊乱的程度.Objective To explore the changes of serum lectin-iike oxidized low-density lipoprotein receptor-1 (LOX-1) and the level of lipids in patients with obstructive sleep apnea hypopnea syndrome (OSAHS). Methods A total of 94 candidates with sleep disorders between January-July 2011 at outpatient department were monitored with polysomnography. According to apnea-hypopnea index (AHI) , they were divided into mild-to-moderate OSAHS ( 5 ~〈 AHI ~〈 30) ( n = 27 ), severe OSAHS ( AHI 〉 30) ( n = 37 ) and normal control groups (AHI 〈 5 ) (n = 30 ). After polysomnography, their blood samples were obtained to measure the levels of serum LOX-1, triglycerides (TG), cholesterol (TC), high-density lipoprotein (HDL-C) and low-density lipoprotein (LDL-C). Results The serum level of LOX-1 in severe OSAHS group was significantly higher than that in the mild-to-moderate and control groups (P 〈 0.01 ). The serum level of LOX-I in OSAHS patients was positively correlated with AHI and longest apnea time ( LAT ) ( r = 0. 645 & 0. 501 respectively, both P 〈 0.0l ) and was negatively correlated with SaO2 ( r = - 0. 647, P〈0.01). No significant difference existed in serum lipids in all groups (P 〉 0. 05). Conclusions Intermittent hypoxia caused by OSAHS increases the level of LOX-1 to further promote the formation and development of atherosclerotic in patients with OSAHS. The levels of lipid can not effectively predict the severitv of lipid metabolism disorder in patients with OSAHS.
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