Literature DB >> 33088647

Severe hypoglycemia caused by a small dose of repaglinide and concurrent use of nilotinib and febuxostat in a patient with type 2 diabetes.

Hitomi Komatsu1, Mariko Enomoto1, Hisashi Shiraishi1, Yasuyo Morita1, Daisuke Hashimoto2, Shuichi Nakayama2, Shogo Funakoshi2, Seiki Hirano2, Yoshio Terada2, Mitsuhiko Miyamura1, Shimpei Fujimoto2.   

Abstract

Repaglinide, an oral hypoglycemic agent, is a short-acting insulin secretagogue. We describe a case, in which an extremely low dose of repaglinide caused severe hypoglycemia and novel drug interactions are suggested. A 71-year-old man with type 2 diabetes was taken to the hospital due to consciousness disorder caused by severe hypoglycemia. He was taking repaglinide 0.25 mg once in the morning with nilotinib 400 mg/day and febuxostat 20 mg/day. Endogenous insulin secretion was not suppressed even in hypoglycemia. Detection of plasma repaglinide 10 h after administration in this case indicates delayed elimination of the agent, which might be derived from reduced hepatocyte uptake due to inhibitory effects of nilotinib on OATP1B1 and reduced oxidation of the agents by inhibitory effects of nilotinib, mainly on CYP3A4 activities, and of febuxostat on CYP2C8 activities. Repaglinide is eliminated by the liver, and is a short-acting insulin secretagogue with a good safety profile in patients with type 2 diabetes complicated by renal impairment, including elderly patients; however, its delayed elimination due to drug-drug interactions should be noted. © The Japan Diabetes Society 2020.

Entities:  

Keywords:  Drug–drug interaction; Febuxostat; Hypoglycemia; Nilotinib; Repaglinide

Year:  2020        PMID: 33088647      PMCID: PMC7538475          DOI: 10.1007/s13340-020-00434-w

Source DB:  PubMed          Journal:  Diabetol Int        ISSN: 2190-1678


  22 in total

1.  Polymorphic organic anion transporting polypeptide 1B1 is a major determinant of repaglinide pharmacokinetics.

Authors:  Mikko Niemi; Janne T Backman; Lauri I Kajosaari; Julian B Leathart; Mikko Neuvonen; Ann K Daly; Michel Eichelbaum; Kari T Kivistö; Pertti J Neuvonen
Journal:  Clin Pharmacol Ther       Date:  2005-06       Impact factor: 6.875

2.  Effects of gemfibrozil, itraconazole, and their combination on the pharmacokinetics and pharmacodynamics of repaglinide: potentially hazardous interaction between gemfibrozil and repaglinide.

Authors:  M Niemi; J T Backman; M Neuvonen; P J Neuvonen
Journal:  Diabetologia       Date:  2003-02-27       Impact factor: 10.122

Review 3.  Severe hypoglycaemia and cardiovascular disease: systematic review and meta-analysis with bias analysis.

Authors:  Atsushi Goto; Onyebuchi A Arah; Maki Goto; Yasuo Terauchi; Mitsuhiko Noda
Journal:  BMJ       Date:  2013-07-29

4.  Cyclosporine markedly raises the plasma concentrations of repaglinide.

Authors:  Lauri I Kajosaari; Mikko Niemi; Mikko Neuvonen; Jouko Laitila; Pertti J Neuvonen; Janne T Backman
Journal:  Clin Pharmacol Ther       Date:  2005-10       Impact factor: 6.875

5.  Risk of Hypoglycemia and Concomitant Use of Repaglinide and Clopidogrel: A Population-Based Nested Case-Control Study.

Authors:  Yun Wei; Fang-Ju Lin; Shin-Yi Lin; Chi-Chuan Wang
Journal:  Clin Pharmacol Ther       Date:  2019-07-23       Impact factor: 6.875

6.  Safety and efficacy of repaglinide in type 2 diabetic patients with and without impaired renal function.

Authors:  Christoph Hasslacher
Journal:  Diabetes Care       Date:  2003-03       Impact factor: 19.112

7.  Effects of intensive glucose lowering in type 2 diabetes.

Authors:  Hertzel C Gerstein; Michael E Miller; Robert P Byington; David C Goff; J Thomas Bigger; John B Buse; William C Cushman; Saul Genuth; Faramarz Ismail-Beigi; Richard H Grimm; Jeffrey L Probstfield; Denise G Simons-Morton; William T Friedewald
Journal:  N Engl J Med       Date:  2008-06-06       Impact factor: 91.245

8.  The CYP2C8 inhibitor trimethoprim increases the plasma concentrations of repaglinide in healthy subjects.

Authors:  Mikko Niemi; Lauri I Kajosaari; Mikko Neuvonen; Janne T Backman; Pertti J Neuvonen
Journal:  Br J Clin Pharmacol       Date:  2004-04       Impact factor: 4.335

9.  Glucuronidation converts clopidogrel to a strong time-dependent inhibitor of CYP2C8: a phase II metabolite as a perpetrator of drug-drug interactions.

Authors:  A Tornio; A M Filppula; O Kailari; M Neuvonen; T H Nyrönen; T Tapaninen; P J Neuvonen; M Niemi; J T Backman
Journal:  Clin Pharmacol Ther       Date:  2014-06-27       Impact factor: 6.875

10.  The tyrosine kinase inhibitor nilotinib selectively inhibits CYP2C8 activities in human liver microsomes.

Authors:  Min-Jung Kim; Jae-Won Lee; Kyung-Suk Oh; Chang-Soo Choi; Kwang Hee Kim; Won Seok Han; Chang-No Yoon; Eun Sook Chung; Dong-Hyun Kim; Jae-Gook Shin
Journal:  Drug Metab Pharmacokinet       Date:  2013-04-30       Impact factor: 3.614

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