Department of Public Health, Grenoble University Hospital, Grenoble, France.
Ann Pharmacother. 2010 Apr;44(4):764-7. doi: 10.1345/aph.1M597. Epub 2010 Mar 2.
To report a case of clinically significant hypoglycemia attributed to the concomitant use of trimethoprim/sulfamethoxazole (TMP/SMX) and repaglinide by a diabetic patient.
A 76-year-old diabetic patient with impaired renal function and no history of hypoglycemia was receiving treatment with repaglinide 1 mg 3 times daily. Five days after TMP/SMX therapy was started for a urinary tract infection, the man developed symptomatic hypoglycemia. Repaglinide and TMP/SMX were stopped and intravenous D-glucose was administered to normalize glucose levels. Repaglinide, but not TMP/SMX, was reintroduced 5 days later and no other hypoglycemic episode occurred. Objective causality assessments revealed that the interaction was probable (World Health Organization-Uppsala Monitoring Centre) or possible (Horn Drug Interaction Probability Scale).
This interaction between TMP/SMX and repaglinide was predictable according to available pharmacokinetic data in healthy subjects. Trimethoprim induced CYP2C8 inhibition, thus increasing the plasma concentration of repaglinide. This interaction is mentioned in the repaglinide product information. To our knowledge, however, no case of symptomatic hypoglycemia associated with a combination of repaglinide and trimethoprim has been described before. This discrepancy may be explained by the subtherapeutic dosage used in the pharmacokinetic study. Moreover, our patient had impaired renal function, which may have led to trimethoprim accumulation and potentiated its interaction with repaglinide. A direct lowering of blood glucose levels due to sulfamethoxazole, also potentiated by renal failure, could also be involved in triggering hypoglycemia.
This interaction between TMP/SMX and repaglinide may have involved inhibition of CYP2C8 by trimethoprim. Clinicians should be aware that this association may lead to symptomatic hypoglycemia, particularly in patients with renal dysfunction.
报告一例因糖尿病患者同时使用甲氧苄啶/磺胺甲噁唑(TMP/SMX)和瑞格列奈而导致临床显著低血糖的病例。
一名 76 岁的糖尿病患者,肾功能受损,无低血糖病史,每日接受瑞格列奈 1 毫克,每日 3 次治疗。在开始治疗尿路感染的 TMP/SMX 治疗 5 天后,该男子出现症状性低血糖。停用瑞格列奈和 TMP/SMX,并给予静脉 D-葡萄糖以使血糖水平正常化。5 天后重新开始使用瑞格列奈,但未再发生其他低血糖事件。客观因果关系评估显示,这种相互作用是可能的(世界卫生组织-乌普萨拉监测中心)或可能的(Horn 药物相互作用可能性量表)。
根据健康受试者的可用药代动力学数据,TMP/SMX 和瑞格列奈之间的这种相互作用是可以预测的。甲氧苄啶诱导 CYP2C8 抑制,从而增加瑞格列奈的血浆浓度。瑞格列奈的产品信息中提到了这种相互作用。然而,据我们所知,以前没有描述过与瑞格列奈和甲氧苄啶联合使用相关的症状性低血糖病例。这种差异可能是由于药代动力学研究中使用的治疗剂量较低。此外,我们的患者肾功能受损,这可能导致甲氧苄啶蓄积并增强其与瑞格列奈的相互作用。磺胺甲噁唑也可能因肾功能衰竭而直接降低血糖水平,从而导致低血糖。
TMP/SMX 和瑞格列奈之间的这种相互作用可能涉及甲氧苄啶对 CYP2C8 的抑制。临床医生应注意到,这种关联可能导致症状性低血糖,特别是在肾功能受损的患者中。