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作 者:杜炜[1] 代云龙[1] 朱洪连 李健[1] 董艳平[1]
出 处:《新医学》2000年第7期404-405,共2页Journal of New Medicine
摘 要:目的:探讨肝硬化患者糖代谢及胰岛β细胞分泌功能的变化。方法:对21名正常人和71例肝硬化患者进行葡萄糖耐量试验、胰岛素和C肽释放试验,肝硬化组按葡萄糖耐量试验结果分为4小组。分别比较空腹及2小时的血糖、胰岛素和C肽水平。结果:肝硬化糖代谢异常总发生率占69%(49/71)。糖耐量减低组空腹及2小时的胰岛素、C肽水平等4项指标高(与其余各组相比,P<0.01),但随着糖代谢紊乱程度的逐渐加重而减少,在重型糖尿病组此4项指标呈显著低水平(与其余各组相比,P<0.01或P<0.05)。结论:肝硬化有较高的糖代谢异常发生率。肝硬化病人存在严重的胰岛素抵抗和高胰岛素血症。胰岛素抵抗和高胰岛素血症可能是β细胞分泌功能紊乱和肝源性糖尿病发生、发展的重要原因。To investigate the changes of glucose metabolism and secretory function of islet β-cell in liver cirrhosis. Methods: Tests for oral glucose tolerance(OGTT),insulin level and C-peptide release were performed in 71 liver cirrhosis patients and 21 controls .Patients were subdivided into four groups according to OGTT. Insulin and C-peptide at fasting and 2h after meal were compared. Results: The prevalence of abnormal glucose metabolism in cirrhosis was 69%(49/71). Insulin and C-peptide level at fasting and 2h after meal in impaired glucose tolerance subgroup were the highest (p<0.01) compared to other group, which decreased gradu- ally as glucose metabolism disorder worsened and reached the lowest levels in severe diabetes (P<0.01 or 0.05, compared to other subgroups). Conclusion: There is high prevalence of abnormal glucose metabolism, severe insulin resistance (IR) and hyperinsulinemia (HIS)in liver cirrhosis. IR and HIS may play important roles in β-cell secretory function disorder, contributing to occurrence and development of hepatic diabetes.
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