摘要
目的 探讨瑞舒伐他汀对代谢综合征(MS)患者颈动脉内膜中层厚度(CIMT)及血管内皮功能的影响.方法 选择2015年11月至2016年12月海阳市人民医院收治的MS患者86例,将其分为瑞舒伐他汀组(10 mg/d)和生活方式干预组,随访6个月,超声检测CIMT及肱动脉内径,血液学检测内皮素-1(ET-1)、一氧化氮(NO)、同型半胱氨酸(Hcy)、超敏C-反应蛋白(hs-CRP)、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、白细胞介素-18(IL-18)水平,比较两组试验前后各指标的差异.结果 治疗后6个月,瑞舒伐他汀组与治疗前比较,最大CI-MT及ET-1、Hcy、hs-CRP、TNF-α、IL-6、IL-18水平均降低(P均〈0.05),而NO水平升高(P〈0.05),充血后肱动脉内径增大(P〈0.05);与生活方式干预组比较,瑞舒伐他汀组上述指标均有显著改善(P均〈0.05).瑞舒伐他汀组无严重不良反应.结论 瑞舒伐他汀可逆转CIMT,改善血管内皮功能,抑制炎症反应,安全性良好.
Objective To study the influence of rosuvastatin on carotid intima-media thickness ( CIMT) and vascular endothelial function in patients with metabolic syndrome ( MS) .Methods Eighty-six patients with MS admitted to Haiyang People 's Hospital from November 2015 to December 2016 were selected and were divided into rosuvastatin group ( receiving rosuvastatin 10 mg/d ) and life style-intervented group , pateints were followed up for 6 months continuosly .Ultrasound indicators , including CIMT and brachial artery diameter , and blood indicators including endothelin-1 ( ET-1 ) , nitric oxide ( NO) , homocysteine ( Hcy ) , high-sensitivity C-reactive protein ( hs-CRP ) , tumor necrosis factor-α( TNF-α) , interleukin-6 ( IL-6) , interleukin-18 ( IL-18) were measured and compared before and after treatment.Results After 6-month treatment, the maximal CIMT and levels of ET-1, Hcy, hs-CRP, TNF-α, IL-6 and IL-18 were significantly decreased ( P all 〈0.05) , while NO level and brachial artery diameter were significantly increased in rosuvastatin group ( P〈0.05 ) . Compared with life style-intervente d group , there were significant improvements of the above indicators in rosuvastatin group ( P〈0.05 ) .There was no serious adverse event in rosuvastatin group .Conclusions Rosuvastatin can reverse CIMT, improve vascular endothelial function and inhibit imflammatory response , and it is safe .
作者
刘微微
李波
Liu Weiwei;Li Bo(Haiyang People's Hospital,Haiyang 265100,China)
出处
《中国实用医刊》
2018年第19期109-112,共4页
Chinese Journal of Practical Medicine
关键词
瑞舒伐他汀
代谢综合征
颈动脉内膜中层厚度
血管内皮功能
炎症
Rosuvastatin
Metabolic syndrome
Carotid intima-media thickness
Vascular endothelial function
Inflammation