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初发2型糖尿病患者强化胰岛素治疗与多次胰岛素注射疗效对比研究 被引量:8

Efficacy of intensive insulin therapy and multiple insulin injections on early-onset type 2 diabetes
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摘要 目的:探讨对于初发2型糖尿病患者,短期胰岛素强化治疗及多次皮下注射对胰岛β细胞及血糖控制的影响,并探讨其机制。方法:回顾性分析2011~2012年在本院住院的58例初诊2型糖尿病患者,经胰岛素泵强化治疗(CSⅡ)和多次皮下注射胰岛素(MSⅡ)两种方法,通过自身前后对比和组间比较,分析高血糖刺激的胰岛素第一时相的分泌、糖化血红蛋白含量、糖耐量实验(OGTT)、体重指数(BMI)等指标。结果:两组患者之间及与自身治疗前比较,空腹血糖(FPG)、餐后2小时血糖(2hPG)下降,平均血糖达标天数减少,均有统计学意义(P<0.05),两组治疗前比较,血中空腹C肽产生无统计学差异,各自治疗前后比较,差异有统计学意义(P<0.05);糖化血红蛋白(HbAc1)与体重指数治疗前后自身对比及组间比较,差异无统计学意义(P>0.05)。结论:初诊糖尿病患者短期胰岛素强化治疗,可以显著改善代表胰岛β细胞功能的胰岛素第一时相分泌,且血糖控制的更平稳,发生低血糖不良反应比例较少,使糖尿病患者胰岛素功能可以恢复到糖尿病病程的更早期阶段,这可能是通过减少β细胞毒性的机制实现的。 Objective:To investigate the efficacy and the mechanism of intensive insulin therapy and multiple insulin injections on treating early-onset type 2diabetes.Methods:Clinical data of 58cases with early-onset type 2diabetes admitted from 2011to 2012were retrospectively analyzed.They were treated by Insulin pump intensive treatment(CSⅡgroup)or continuous subcutaneous insulin infusion(MSⅡ group).Fasting plasma glucose(FPG),2hPG,fasting plasma C-peptide in plasma,BMI,OGTT before and after the treatment were measured and compared between CSⅡ and MSⅡ groups.Results:After treatments,FPG,2hPG,the time for normal glucose were decreased significantly(P0.05),and the differences in these indexes were significant between two groups(P0.05).Before the treatment,there was no significant difference in fasting plasma C-peptide between two groups,but the difference was significant after treatment(P0.05).After treatment,there was no significant changes in HbAc1and BMI,and the differences were not significant between two groups(P0.05).Conclusions:Short-term insulin treatment can significantly improve insulin secretion at the first phase,which is more stable and of few side reactions such as hypoglycemia.It may be associated with reduce toxicity of β cells.
出处 《海南医学院学报》 CAS 2013年第10期1424-1427,共4页 Journal of Hainan Medical University
基金 中国高校医学期刊临床专项资金项目(112210821)~~
关键词 2型糖尿病 胰岛素强化治疗 葡萄糖耐量试验 胰岛β细胞 Diabetes mellitus type2 Intensive insulin therapy HbA1c Islet beta cells
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