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沙格列汀对2型糖尿病Nesfatin-1分泌及代谢调节的临床研究
引用本文:陈宽林,卓铁军,王健,梅青.沙格列汀对2型糖尿病Nesfatin-1分泌及代谢调节的临床研究[J].中国现代医学杂志,2016,26(13):68-74.
作者姓名:陈宽林  卓铁军  王健  梅青
作者单位:1.江苏建康职业学院 全科医学教研室,江苏 南京 211800;2.江苏省老年医院,江苏 南京 210024;3.江苏省南京市红花卫生服务中心,江苏 南京 210001;4.江苏省南京市秦虹卫生服务中心,江苏 南京 210006
摘    要:

目的  沙格列汀能有效改善2型糖尿病(T2DM)糖代谢,Nesfatin-1是摄食行为和能量代谢调节的重要因子。为探讨沙格列汀对T2DM患者Nesfatin-1分泌调节及糖脂代谢、血压调节的作用,观察其治疗前后Nesfatin-1水平变化,并与同期其他非二基肽酶-4(DPP-4)抑制剂治疗患者进行比较。方法  门诊治疗的T2DM患者102例(男∶女=48:54),其中治疗组51例(男∶女=24∶27)使用包含沙格列汀口服降糖药物;同期51例(男∶女=24∶27)未使用DPP-4抑制剂治疗的T2DM患者作为对照组。观察和比较基线及3、6和12个月时Nesfatin-1、C-肽(C-P)、稳态β细胞功能评价指数(HOMA-β)、稳态胰岛素评价指数(HOMA-IR)、糖化血红蛋白A1c(HbA1c)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、体重指数(BMI)及血压变化。结果  治疗组血清Nesfatin-1分泌上调,C-P水平升高,显著改善HOMA-IR、HOMA-β以及糖脂代谢,降低BMI和血压。单因素直线回归分析显示,Nesfatin-1与HOMA-β、C-P以及HDL-C呈正相关,与其他指标呈负相关。结论  沙格列汀能促进T2DM患者Nesfatin-1分泌,有效改善胰腺β细胞功能、胰岛素抵抗及糖脂代谢,降低BMI和调节血压。沙格列汀可以通过上调Nesfatin-1分泌,在T2DM患者中发挥潜在的重要作用。



关 键 词:

沙格列汀  Nesfatin-1  2型糖尿病  稳态胰岛素评价指数  稳态&beta  细胞功能评价指数

收稿时间:2015/12/7 0:00:00

Effect of Saxagliptin on regulation of nesfatin-1 secretion and metabolism in type 2 diabetes mellitus patients
Kuan-lin Chen,Tie-jun Zhuo,Jian Wang,Qing Mei.Effect of Saxagliptin on regulation of nesfatin-1 secretion and metabolism in type 2 diabetes mellitus patients[J].China Journal of Modern Medicine,2016,26(13):68-74.
Authors:Kuan-lin Chen  Tie-jun Zhuo  Jian Wang  Qing Mei
Institution:1. General Medicine Teaching and Research Section, Jiangsu Jiankang Vocational College, Nanjing, Jiangsu 211800, China; 2. Jiangsu Provincial Geriatric Hospital, Nanjing, Jiangsu 210024, China; 3. Honghua Health Center, Nanjing, Jiangsu 210001, China; 4. Qinhong Health Center, Nanjing, Jiangsu 210006, China
Abstract:

Objective To investigate the effect of Saxagliptin on regulating nesfatin-1 secretion and metabolism by observing the levels of the nesfatin-1 and other parameters in type 2 diabetes mellitus (T2DM) patients before and after Saxagliptin treatment. Methods A total of 102 T2DW participants (M : F = 48 : 54) were investigated. The 51 patients (M : F = 24 : 27) in the treatment group were treated with oral glucose-lowering drugs including Saxagliptin, the 51 patients (M : F = 24 : 27) in the control group were treated with oral glucose-lowering agents excluding all DPP-4 inhibitors. Serum nesfatin-1, C-peptide, HOMA-β function, HOMA-IR, HbA1c, LDL-C, HDL-C, BMI and blood pressure at baseline and in 3, 6 and 12 months of treatment were observed and compared. Results Saxagliptin significantly up-regulated nesfatin-1 secretion, increased serum C-peptide; improved HOMA-IR, HOMA-β function, glucose and lipid metabolisms; and reduced BMI and blood pressure. Simple linear regression analysis revealed that serum nesfatin-1 was positively correlated with HOMA-β function, C-peptide and HDL-C, while negatively correlated with the rest parameters. Conclusions Saxagliptin could up-regulate nesfatin-1 secretion, ameliorate islet β-cell''s function and insulin resistance as well as the glucose and lipid metabolisms, lower BMI and blood pressure in patients with type 2 diabetes mellitus. As one of the DPP-4 inhibitors, Saxaglitin has the potential to play fundamental roles in type 2 diabetes mellitus by up-regulating nesfatin-1 secretion besides lowering glucose through inhibiting the degradation of GLP-1.

Keywords:

Saxagliptin  nesfatin-1  type 2 diabetes mellitus  homeostasis model assessment-insulin resistance  HOMA-&beta  function

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