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作 者:吴美芬[1] 武革[1] 蔡晓玲[1] 陈晓铭[1] 方烁[1] 潘海燕[1]
机构地区:[1]广东医学院附属医院内分泌科,湛江524001
出 处:《中国临床新医学》2013年第8期736-739,共4页CHINESE JOURNAL OF NEW CLINICAL MEDICINE
基 金:广东省科技计划资助项目(编号:2011B031800231);广东省医学科研基金资助项目(编号:B2011243)
摘 要:目的探讨初发2型糖尿病(T2DM)患者血胰高血糖素样肽-1(GLP-1)对胰高血糖素及早相胰岛素分泌的影响。方法以新发T2DM患者(T2DM组)、健康体检者(对照组)为研究对象,采用标准馒头餐试验,观察空腹、进餐后30 min、120 min静脉血浆GLP-1动态变化及对血浆葡萄糖、胰高血糖素、胰岛素分泌的影响。结果初发T2DM组患者馒头餐各时点GLP-1水平均分别较对照组显著降低,差异有统计学意义(P<0.05),馒头餐后30 min、120 min胰岛素水平显著降低(P<0.05),但空腹胰岛素无明显差异(P>0.05);而胰高血糖素则较对照组各时点显著升高,差异有统计学意义(P<0.05)。初发T2DM组早相胰岛素分泌指数(ΔFINS30/ΔG30)显著低于对照组,差异有统计学意义(P<0.05)。结论初发T2DM患者存在GLP-1分泌减少,GLP-1缺乏可能是T2DM患者胰岛β细胞分泌缺乏及胰高血糖素分泌过多的重要因素。Objective To explore the effects of the change of Glucagon-like peptide-1 level on glucagon and early phase insulin secretion in the patients with the newly diagnosed type 2 diabetes.Methods Patients with the newly diagnosed type 2 diabetes(T2DM group) and healthy volunteers(control group) were used as the research object,and the standardized bread meal test was used to observe effects of the dynamic changes of GLP-1 level at 0 min,30 min and 120 min on plasma glucose,glucagon and insulin secretion.Results The levels of GLP-1 at each time point in newly diagnosed T2DM group were significantly reduced compared with those of the control group respectively(P &lt; 0.05);The levels of insulin at 30 min and 120 min were both significantly reduced compared with those of the control group respectively(P &lt; 0.05),but the difference had no statistical significance at 0 min between two groups(P &gt; 0.05);The levels of glucagon at each time point in newly diagnosed T2DM group were significantly higher than that of the control group(P &lt; 0.05).The first-phase insulin secretion index of newly diagnosed T2DM group was significantly reduced compared with those of the control group(P &lt; 0.05).Conclusion The levels of GLP-1 at each time point in newly diagnosed patients with type 2 diabetes mellitus were significantly reduced;GLP-1 dificiency might be the important factors of lack of islet beta cell secretion and insrease of glucagon secretion.
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