检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:商丽娜[1] 李华[1] 杨再刚[1] 翟倩倩[1] 冯涛[1] 姜丹[1] 田勇
机构地区:[1]郑州大学第一附属医院老年内分泌科,河南省郑州市450052 [2]郑州市人民医院特需病房
出 处:《中国全科医学》2012年第12期1326-1328,1331,共4页Chinese General Practice
摘 要:目的观察2型糖尿病(T2DM)患者血浆脂蛋白相关磷脂酶A2(Lp-PLA2)水平,探讨其与T2DM大血管并发症的关系及临床意义。方法选取69例T2DM患者,其中单纯糖尿病患者31例(单纯糖尿病组)、糖尿病合并大血管病变患者38例(糖尿病并大血管病变组),另选取同期在我院体检的21例健康者为对照组。采用ELISA法检测3组受检者血浆Lp-PLA2水平,并进行比较。结果单纯糖尿病组和糖尿病并大血管病变组患者血浆Lp-PLA2水平显著高于对照组(P<0.05),且糖尿病并大血管病变组Lp-PLA2水平又显著高于单纯糖尿病组(P<0.05)。Lo-gistic回归分析显示:除去混杂因素后,Lp-PLA2水平仍与糖尿病大血管病变直接相关(P<0.05)。结论 Lp-PLA2是糖尿病的独立危险因素之一,对预测糖尿病血管并发症有一定的意义。Objective To explore the correlation between the levels of lipoprotein - associated phospholipase A2 ( Lp - PEA2 ) and macrovascular complications in type 2 diabetes mellitus. Methods 69 patients with T2DM were divided into T2DM without macrovascular complication group (31 cases) and T2DM with maerovascular complication group (38 cases ). Mean- while, 21 healthy people who received physical examination were selected as control group. ELISA was used to detect the plasma levels of Lp - PLA2 in the three groups. Results The Lp - PEA2 level of T2DM without maerovascular complication group and T2DM with macrovascular complication group was significantly higher than that in control group (P 〈 0. 05 ) , and Lp - PLA2 lev- el of T2DM with maerovaseular group was significantly higher than that of T2DM without maerovaseular group ( P 〈 0. 05 ). Lo- gistic regression analysis showed that after removing the confounding factors, Lp - PLA2 still directly related to macrovaseular complications of diabetes ( P 〈 0.05 ) . Conclusion Lp - PLA2 level is one of the independent risk factors for diabetes mellitus, and can serve as a biomarker for predicting the early vascular complications in patients with type 2 diabetes mellitus.
关 键 词:糖尿病 2型 脂蛋白相关磷脂酶A2 糖尿病血管病变
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.222