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机构地区:[1]南通市第二人民医院检验科,江苏南通226002 [2]南通市第二人民医院内分泌科,江苏南通226002
出 处:《现代检验医学杂志》2016年第2期108-111,共4页Journal of Modern Laboratory Medicine
摘 要:目的比较不同糖化血红蛋白(HbAlc)水平的2型糖尿病(T2DM)患者胰岛素分泌和胰岛素抵抗情况,了解葡萄糖毒性对胰岛口细胞分泌功能的影响。方法将137例T2DM患者,按HbAlc水平分为4组,即A组(HbAlc≤70),B组(7%〈HbAlc≤9%),C组(9%〈HbAlc≤11%)和D组(HbAlc〉11%),测定各组空腹血糖(FPG),HbAlc及精氨酸刺激前后各时点的胰岛素(INS)。用稳态模型评估法评价基础胰岛素分泌功能(HOMA-β)和胰岛素抵抗指数(HOMA-IR),并用精氨酸刺激后血糖校正胰岛素增值(△INS/FPG)评估第一相胰岛素分泌功能。结果各组T2DM患者FPG差异均有统计学意义(F=15.633~106.154,P值均〈0.01),且与HbAlc呈正相关(r=0.627,P〈0.01);HOMA—β和△INS/FPG均表现为A组、B组分别与其他各组差异有统计学意义(F=4.106~16.255,P值均〈0.05),但c组与D组之间差异无统计学意义(F=0.761,2.756,P值均〉0.05);A组HOMA-IR与C组、D组之间差异有统计学意义(F=4.836,8.524,P值均〈0.05);精氨酸刺激后胰岛素分泌不足检出率在HbAlc〉9%时明显升高。结论胰岛B细胞功能的判断受长期糖毒性的干扰,故将T2DM患者的HbAlc控制在9%以下进行胰岛素分泌功能评估及精氨酸刺激试验,能较为准确地反映胰岛p细胞功能。Objective To compare insulin secretion and Insulin resistance of type 2 diabetic patients with different HbAlc levels,and to evaluate the effect of glucose toxicity on the islet β cell response. Methods 137 cases type 2 diabetes mellitus (T2DM) patients were divided into 4 groups according to HbAlc levels:group A with HbAlc≤7% ,group B with 7% HbAlc≤9 %, group C with 9 % 〈 HbA1 c≤ 11 % and group D with HbA1 c〉 11%. Detected fasting blood glucose (FPG), HbAlc and each time point of insulin (INS) after arginine stimulation. Homeostasis model assessment was used to evaluate basal insulin secretion (HOMA-β) and insulin resistance (HOMA-IR). The incremental value of insulin by blood glucose corrected (AINS/FPG) after arginine stimulation was used to evaluate the first phase insulin secretion. Results The level of FPG had significant differencein each group of T2DM patients (F= 15. 633- 106. 154, P〈0.01), and was positively correlated with HbAlc (r=0. 627,P〈0.01). The level of HOMA-β and △INS/FPG were showed that group A and B were statistical significant difference with the other groups (F= 4. 106 - 16.255, P〈0.05), but the difference was not statistical significant between group C and group D (F=0. 761,2. 756 ,P)0.05). The level of HOMA-IR in group A was statistical significant comparing group C and group D (F= 4. 836,8. 524, P〈0.05). After arginine stimulation, the detection rate of the decreased function of insulin secretion increased significantly with HbAlc 〉9 %. Conclusion The measurement of islet cell's function was influenced by long-term high glucose toxicity. Therefore, patients with T2DM, which the level of H bAlc was less than 9 %, were conducted with insulin secretion function evaluation and arginine stimulation test, this could reflect the function of islet βcell more accurately.
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