Irsigler K, Ogris E, Steinhardt T, Brändle J, Regal H, Zdolsek I
Wien Klin Wochenschr. 1979 Aug 31;91(16):541-50.
The purpose of the study was to investigate whether the potency of effect on the beta cell differs with type of sulfonylurea (SU) and with degree of severity of diabetes. 12 maturity onset diabetics were classed according to fasting blood glucose (FBG) in three groups of 4 patients each. Each patient served as his own control. Glibenclamide, Gliquidone, Glusoxepide and placebo were administered in random order with degree dosage adjusted according to degree of severity of diabetes. All patients were given a standardized diet with 150 g carbohydrates per day. Fullday profiles of blood glucose, insulin, C-peptide and sulfonylurea level in serum were made on the third day under each preparation. Results showed that with proper nutrition and sufficient weight reduction, patients in group I (FBG 80--130 mg/dl) needed no oral medication and in fact showed a tendency towards hypoglycaemic episodes under oral therapy. In group II (FBG 130--200 mg/dl) the effect of nutrients on beta cell secretion appeared to be both enhanced and accelerated by SU administration. Satisfactory metabolic control was achieved with SU, but not with placebo. This group seems to represent the type of patient most likely to benefit from SU therapy. In spite of high dosage levels, satisfactory control was not achieved with SU in any patient in group III (FBG greater than 200 mg/dl). Depending on individual factors such as ketosis-proneness, vascular complications, age and psycho-social aspects, insulin administration should be considered for these patients. There were not differences between the individual SU preparations in the parameters studied. There was insufficient evidence for a pharmacokinetic differential diagnosis.
本研究的目的是调查不同类型的磺脲类药物(SU)对β细胞的作用效力是否因糖尿病严重程度而异。12名成年起病的糖尿病患者根据空腹血糖(FBG)分为3组,每组4例。每位患者均以自身作为对照。格列本脲、格列喹酮、葡糖昔脲和安慰剂随机给药,给药剂量根据糖尿病严重程度进行调整。所有患者均给予每天含150克碳水化合物的标准化饮食。在每种制剂治疗的第3天,测定患者全天的血糖、胰岛素、C肽和血清磺脲类药物水平。结果显示,在营养适当且体重充分减轻的情况下,I组(FBG 80 - 130mg/dl)患者无需口服药物治疗,实际上在口服治疗期间有发生低血糖事件的倾向。在II组(FBG 130 - 200mg/dl)中,SU给药似乎增强并加速了营养物质对β细胞分泌的作用。使用SU可实现满意的代谢控制,但使用安慰剂则不能。该组似乎代表了最有可能从SU治疗中获益的患者类型。尽管III组(FBG大于200mg/dl)的所有患者均使用了高剂量的SU,但仍未实现满意的控制。根据个体因素,如酮症倾向、血管并发症、年龄和心理社会因素,应考虑对这些患者使用胰岛素治疗。在所研究的参数方面,各SU制剂之间没有差异。没有足够的证据进行药代动力学鉴别诊断。