Lundershausen R, Orban S, Pissarek D, Panzram G
Poliklinik für Innere Medizin, Medizinischen Akademie Erfurt, Deutsche Demokratische Republik.
Wien Klin Wochenschr. 1987 Sep 11;99(17):603-8.
The long-term efficacy of combined insulin-glibenclamide treatment was investigated in 79 secondary drug failure patients by means of a double-blind, randomized placebo-controlled study. During a one-year follow-up period the patients on insulin plus glibenclamide required significantly lower exogenous insulin doses. Coincidentally, C-peptide concentrations were significantly raised in the verum versus the placebo group. Additionally, the administration of glibenclamide resulted in a decreased level of hyperglycaemia during the first six months of the observation period. Glibenclamide withdrawal after six and again after twelve months of the combined therapy provoked a deterioration of glycaemic control, as well as a lowering of the C-peptide concentrations. The findings demonstrate a prolonged beneficial effect of the combined treatment, in contrast to the solely short-term effects predicted by numerous studies. The metabolic improvement must be ascribed in part to the beta-cytotropic effect of glibenclamide. Extrapancreatic pathways via receptor/postreceptor mechanisms cannot be excluded.
通过双盲、随机、安慰剂对照研究,对79例继发性药物失效患者联合胰岛素与格列本脲治疗的长期疗效进行了调查。在一年的随访期内,接受胰岛素加格列本脲治疗的患者所需外源性胰岛素剂量显著降低。巧合的是,与安慰剂组相比,治疗组的C肽浓度显著升高。此外,在观察期的前六个月,格列本脲的使用使高血糖水平降低。联合治疗6个月和12个月后停用格列本脲,导致血糖控制恶化以及C肽浓度降低。这些发现表明联合治疗具有长期有益效果,这与众多研究所预测的仅短期效果形成对比。代谢改善部分归因于格列本脲的促β细胞作用。不能排除通过受体/受体后机制的胰腺外途径。