Hypoglycemia Associated With Drug-Drug Interactions in Patients With Type 2 Diabetes Mellitus Using Dipeptidylpeptidase-4 Inhibitors

被引:2
|
作者
Ray, Chin-Ying [1 ]
Wu, Victor Chien-Chia [2 ,3 ]
Wang, Chun-Li [2 ,3 ]
Tu, Hui-Tzu [4 ]
Huang, Yu-Tung [4 ]
Kuo, Chang-Fu [3 ,5 ,6 ]
Chang, Shang-Hung [2 ,3 ,4 ]
机构
[1] Chang Gung Mem Hosp, Dept Pharm, Linkou Med Ctr, Taoyuan, Taiwan
[2] Chang Gung Mem Hosp, Div Cardiol, Linkou Med Ctr, Taoyuan, Taiwan
[3] Chang Gung Univ, Coll Med, Taoyuan, Taiwan
[4] Chang Gung Mem Hosp, Ctr Big Data Analyt & Stat, Linkou Med Ctr, Taoyuan, Taiwan
[5] Chang Gung Mem Hosp, Div Rheumatol Allergy & Immunol, Dept Internal Med, Linkou Med Ctr, Taoyuan, Taiwan
[6] Univ Nottingham, Sch Med, Div Rheumatol Orthopaed & Dermatol, Nottingham, England
关键词
dipeptidylpeptidase-4; inhibitors; drug-drug interaction; drug safety; hypoglycemia; diabetes mellifus; DIPEPTIDYL PEPTIDASE-IV; PHARMACOKINETIC INTERACTION; FOCUS; VILDAGLIPTIN; SAXAGLIPTIN; SIMVASTATIN; AGENTS;
D O I
10.3389/fphar.2021.570835
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Dipeptidylpeptidase-4 inhibitors (DPP-4i ' s) are considered to be safe for patients with type 2 diabetes mellitus (T2DM). However, little is known about drug-drug interactions between DPP-4i ' s and concurrent medications. Methods: Data on patients using DPP-4i ' s for T2DM during 2011-2017 were retrieved from Chang Gung Research database provided by Chang Gung Memorial Hospital. Patients were excluded if they were aged 90 years; had incomplete demographic data; had insulinoma; or had records of concomitant insulin use. A generalized estimating equation-based Poisson model was employed for statistical analysis. The primary outcome was hypoglycemia events. Results: We retrieved data on a total of 97,227 patients using DPP-4i ' s. After patients were excluded according to the mentioned criteria, the remaining 77,047 DPP-4i users were studied (mean age 64 +/- 12 years, men 54.4%). The most common medications coprescribed with DPP4is over all person-quarters were acetaminophen, simvastatin, fluvastatin, and colchicine (all >20,000 person-quarters). The combinations of a DPP-4i with bumetanide, captopril, colchicine, acetaminophen, cotrimoxazole, and pantoprazole were associated with an increased risk of hypoglycemia. Compared with the ratios observed for person-quarters of DPP-4i use alone (reference category), the adjusted prevalence ratios per 100 person-years of hypoglycemia for person-quarters of DPP-4i use in combination with bumetanide, captopril, colchicine, acetaminophen, cotrimoxazole, and pantoprazole were 2.44 (95% confidence interval [CI], 1.78-3.36), 2.97 (95% CI, 2.26-3.90), 1.87 (95% CI, 1.44-2.42), 2.83 (95% CI, 2.44-3.29), 2.27 (95% CI, 1.27-4.04), and 3.03 (95% CI, 1.96-4.68), respectively. Conclusion: Among patients taking DPP-4i ' s for T2DM, concurrent use of such inhibitors with bumetanide, captopril, acetaminophen, and pantoprazole was associated with an increased risk of hypoglycemia compared with the use of DPP-4i ' s alone. Physicians prescribing DPP-4i ' s should consider the potential risks associated with their concomitant use with other drugs.
引用
收藏
页数:8
相关论文
共 50 条