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:刘军[1] 查英[1] 王芳[1] 陈灶萍[1] 徐炯[1] 盛励[1] 廖晓寰[2] 郭瑜琳[3]
机构地区:[1]复旦大学附属上海市第五人民医院内分泌科,上海200240 [2]复旦大学附属上海市第五人民医院免疫室,上海200240 [3]复旦大学附属上海市第五人民医院血管超声室,上海200240
出 处:《临床内科杂志》2008年第5期333-335,共3页Journal of Clinical Internal Medicine
摘 要:目的探讨2型糖尿病患者内脏素水平变化及与胰岛抵抗和胰岛β细胞功能之间的关系。方法检测了2型糖尿病患者95例和正常对照组54例内脏素、血脂、血糖和空腹胰岛素(FINS)水平,并评价了颈总动脉内膜中层厚度(IMT)。采用稳态模式(HOMA)评价胰岛素抵抗和胰岛β细胞功能。结果2型糖尿病组胰岛素抵抗指数(HOMA-IR)、颈动脉IMT和内脏素水平高于对照组,胰岛β细胞功能指数(HOMA-β)水平低于对照组(P<0.05)。Spearman相关性分析显示,内脏素与空腹血糖(r=0.496,P=0.000)和HOMA-IR(r=-0.380,P=0.000)呈正相关;与HOMA-β(r=-0.355,P=0.000)呈负相关。多元逐步回归分析显示,内脏素与空腹血糖呈独立正相关(P=0.000)。结论2型糖尿病患者内脏素水平升高,内脏素可能与胰岛素抵抗和胰岛β细胞功能损害有一定相关性。Objective To investigate the relevance of visfatin to insulin resistance and the betacell function in type 2 diabetes mellitus. Methods The plasma visfatin, serum lipids, serum glucose and fasting insulin(FINS) were measured in 95 type 2 diabetes(T2DM) and 54 normal control subjects(NC). The intima-media thickness(IMT) of common carotid arteries were detected by high resolution ultrasound. Homeostasis model assessment(HOMA) was applied to assess the status of insulin resistance and beta-cell function. Results The levels of visfatin,HOMA-IR and IMT of common carotid arteries were significantly elevated and HOMA-β was lower in T2DM group compared with NC group. In all subjects, spearman correlation analysis showed that visfatin was positively correlated to FBG( r = 0.496 ,P = 0.000), HOMA-IR ( r = - 0.380, P = 0.000) and negatively correlated to HOMA-β ( r = - 0. 355, P = 0.000). Multiple stepwise regression analysis showed visfatin were the independent risk factors affected the FBG. Conclusions There was increased plasma visfatin in type 2 diabetes mellitus. Hypervisfatimnia probably related to insulin resistance and beta-cell disfunction.
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:216.73.216.210