Groop L, Schalin C, Franssila-Kallunki A, Widén E, Ekstrand A, Eriksson J
Fourth Department of Medicine, Helsinki University Hospital, Finland.
Am J Med. 1989 Aug;87(2):183-90. doi: 10.1016/s0002-9343(89)80695-3.
Secondary failure to treatment with oral antidiabetic agents frequently occurs in patients with non-insulin-dependent diabetes mellitus. In the search for causes of such failures, we examined patient- and disease-related factors in nonresponders and in responders to treatment with oral antidiabetic agents.
The study population consisted of three groups: (1) 34 nonresponders to treatment with sulfonylureas; (2) 25 patients who still responded to treatment with sulfonylureas; and (3) 10 age-matched healthy control subjects. In addition to patient-related factors such as adherence to diet and knowledge of diabetes, we examined insulin response to a test meal and hepatic and peripheral insulin sensitivity during a euglycemic insulin clamp in combination with indirect calorimetry and infusion of [3H-3-]glucose.
Patient-related factors such as daily nutrient intake, activity score, knowledge of diabetes, and "stress level" were similar in both groups. However, nonresponders had a higher rate of basal hepatic glucose production (4.60 +/- 0.14 versus 3.63 +/- 0.26 mg/minute/kg of lean body weight; p less than 0.001), which was less suppressed by euglycemic hyperinsulinemia (about 100 microU/mL) than was that of the responders (p less than 0.001). In addition, total insulin-stimulated glucose metabolism was reduced (5.07 +/- 0.22 versus 7.09 +/- 0.56 mg/kg.LBM.minute; p less than 0.001), and this was mainly accounted for by a reduction in non-oxidative glucose metabolism (glycogen synthesis and anaerobic glycolysis) (1.78 +/- 0.22 versus 3.54 +/- 0.49 mg/kg.LBM.minute; p less than 0.001). The severity of hepatic and peripheral insulin resistance correlated with the plasma glucose concentration but was unrelated to insulin secretion. In a multiple linear regression analysis, glucose overproduction in the liver (26.1%), impaired peripheral glucose metabolism (17.3%), and insulin deficiency (12.6%) could explain only 56% of the causes of secondary drug failure.
Secondary failure to treatment with oral hypoglycemic agents is determined by the disease itself rather than by patient-related factors. Treatment of secondary drug failure should therefore aim at ameliorating both hepatic and peripheral insulin resistance.
口服抗糖尿病药物治疗继发性失效在非胰岛素依赖型糖尿病患者中经常发生。在探寻此类失效原因的过程中,我们研究了口服抗糖尿病药物治疗无反应者和有反应者的患者相关因素及疾病相关因素。
研究人群包括三组:(1)34例对磺脲类药物治疗无反应者;(2)25例仍对磺脲类药物治疗有反应的患者;(3)10例年龄匹配的健康对照者。除了饮食依从性和糖尿病知识等患者相关因素外,我们还通过正常血糖胰岛素钳夹试验结合间接测热法及[3H-3-]葡萄糖输注,检测了对试验餐的胰岛素反应以及肝脏和外周胰岛素敏感性。
两组患者的每日营养摄入量、活动评分、糖尿病知识和“应激水平”等患者相关因素相似。然而,无反应者基础肝葡萄糖生成率较高(4.60±0.14对3.63±0.26毫克/分钟/千克瘦体重;p<0.001),正常血糖高胰岛素血症(约100微单位/毫升)对其抑制作用比对有反应者小(p<0.001)。此外,胰岛素刺激的总葡萄糖代谢降低(5.07±0.22对7.09±0.56毫克/千克瘦体重·分钟;p<0.001),这主要是由于非氧化葡萄糖代谢(糖原合成和无氧糖酵解)降低所致(1.78±0.22对3.54±0.49毫克/千克瘦体重·分钟;p<0.001)。肝脏和外周胰岛素抵抗的严重程度与血糖浓度相关,但与胰岛素分泌无关。在多元线性回归分析中,肝脏葡萄糖生成过多(26.1%)、外周葡萄糖代谢受损(17.3%)和胰岛素缺乏(12.6%)仅能解释继发性药物失效原因的56%。
口服降糖药物治疗继发性失效由疾病本身决定,而非患者相关因素。因此,继发性药物失效的治疗应旨在改善肝脏和外周胰岛素抵抗。