Impact of sitagliptin combination therapy and hypoglycemia in Japanese patients with type 2 diabetes: a multi-center retrospective observational cohort study.

Beta-blockers, Dipeptidyl-peptidase IV inhibitors Hypoglycemia Type 2 diabetes mellitus

Journal

Journal of pharmaceutical health care and sciences
ISSN: 2055-0294
Titre abrégé: J Pharm Health Care Sci
Pays: England
ID NLM: 101672177

Informations de publication

Date de publication:
2020
Historique:
received: 01 03 2020
accepted: 11 05 2020
entrez: 11 6 2020
pubmed: 11 6 2020
medline: 11 6 2020
Statut: epublish

Résumé

Patients with diabetes are at higher risk of developing polypharmacy because of the high frequency of comorbidities. There have been several reports on the hypoglycemic risk of the combination of hypoglycemic agents and other medications. This study aimed to investigate the hypoglycemic risk of drug-drug interaction between sitagliptin and other oral hypoglycemic agents or antihypertensive agents in Japanese patients with type 2 diabetes. From January 2010 to March 2012, a total of 3247 patients were recruited and evaluated at outpatient clinics at Juntendo University Hospital, other satellite hospitals, and private clinics. This study was a sub-analysis of the Sitagliptin Registration Type 2 Diabetes-Juntendo Collaborating Project. Participants were limited to those treated with oral hypoglycemic agents, excluding insulin users, to investigate the association of the first hypoglycemic events with oral hypoglycemic agents or other medications within 6 months after starting sitagliptin. The factors related to the first hypoglycemic event were analyzed using Cox regression analysis. In total, 2956 patients with a mean age of 65.1 ± 11.3 years were included. A total of 46 hypoglycemic events (1.6%) were observed. One patient had severe hypoglycemia followed by emergency transport to the hospital. Sitagliptin was not associated with hypoglycemia, but its combination with sulfonylurea (hazard ratio: 4.42, 95% confidential interval: 1.36-14.42) or β-blocker (hazard ratio, 3.50, 95% confidential interval: 1.54-7.96) was significantly associated with hypoglycemia. The drug-drug interactions between sitagliptin and sulfonylurea or β-blocker likely increases the hypoglycemic risk in Japanese patients with type 2 diabetes. Pharmacists should consider potential adverse events from drug-drug interaction in type 2 diabetes with polypharmacy, particularly those who are managed by several doctors or clinics.

Sections du résumé

BACKGROUND BACKGROUND
Patients with diabetes are at higher risk of developing polypharmacy because of the high frequency of comorbidities. There have been several reports on the hypoglycemic risk of the combination of hypoglycemic agents and other medications. This study aimed to investigate the hypoglycemic risk of drug-drug interaction between sitagliptin and other oral hypoglycemic agents or antihypertensive agents in Japanese patients with type 2 diabetes.
METHODS METHODS
From January 2010 to March 2012, a total of 3247 patients were recruited and evaluated at outpatient clinics at Juntendo University Hospital, other satellite hospitals, and private clinics. This study was a sub-analysis of the Sitagliptin Registration Type 2 Diabetes-Juntendo Collaborating Project. Participants were limited to those treated with oral hypoglycemic agents, excluding insulin users, to investigate the association of the first hypoglycemic events with oral hypoglycemic agents or other medications within 6 months after starting sitagliptin. The factors related to the first hypoglycemic event were analyzed using Cox regression analysis.
RESULTS RESULTS
In total, 2956 patients with a mean age of 65.1 ± 11.3 years were included. A total of 46 hypoglycemic events (1.6%) were observed. One patient had severe hypoglycemia followed by emergency transport to the hospital. Sitagliptin was not associated with hypoglycemia, but its combination with sulfonylurea (hazard ratio: 4.42, 95% confidential interval: 1.36-14.42) or β-blocker (hazard ratio, 3.50, 95% confidential interval: 1.54-7.96) was significantly associated with hypoglycemia.
CONCLUSIONS CONCLUSIONS
The drug-drug interactions between sitagliptin and sulfonylurea or β-blocker likely increases the hypoglycemic risk in Japanese patients with type 2 diabetes. Pharmacists should consider potential adverse events from drug-drug interaction in type 2 diabetes with polypharmacy, particularly those who are managed by several doctors or clinics.

Identifiants

pubmed: 32518665
doi: 10.1186/s40780-020-00169-5
pii: 169
pmc: PMC7271486
doi:

Types de publication

Journal Article

Langues

eng

Pagination

13

Informations de copyright

© The Author(s) 2020.

Déclaration de conflit d'intérêts

Competing interestsHirotoshi Ohmuara has received lecture fees from Takeda Pharmaceutical Co., MSD K.K., AstraZeneca K.K., and Shionogi & Co. Ltd. and research funds from Pfizer Co., MSD K.K., and Takeda Pharmaceutical Co. Ltd. Hiroyuki Daida has received lecture fees from AstraZeneca K.K., MSD K.K., Kowa Pharmaceutical Company Ltd., Sanofi-Aventis K.K., GlaxoSmithKline K.K., Shionogi & Co. Ltd., Daiichi-Sankyo Company, Limited, Takeda Pharmaceutical Co. Ltd., Mitsubishi Tanabe Pharma Corp., Pfizer Co. Ltd., and Astellas Pharma Inc. and research funds from Takeda Pharmaceutical Co. Ltd., Bristol-Myers Squibb Company, Nippon Boehringer Ingelheim Co. Ltd., Astellas Pharma Inc., Novartis Pharma K.K., MSD K.K., Sanofi-Aventis K.K., Otsuka Pharmaceutical Co. Ltd., Dainippon Sumitomo Pharma Co. Ltd., Pfizer Co. Ltd., Kowa Pharmaceutical Company Ltd., Shionogi & Co. Ltd., AstraZeneca K.K., Teijin Limited, and Morinaga Milk Industry Co. Ltd. Tomoyuki Saito and Shuko Nojiri have nothing to declare.

Références

Am Heart J. 2019 Dec;218:92-99
pubmed: 31715435
N Engl J Med. 2003 Jan 30;348(5):383-93
pubmed: 12556541
J Hum Hypertens. 1997 May;11(5):307-12
pubmed: 9205938
BMJ. 1998 Sep 12;317(7160):713-20
pubmed: 9732338
Hypertension. 2017 Jul;70(1):103-110
pubmed: 28559400
Curr Med Res Opin. 2010 Mar;26(3):615-29
pubmed: 20067434
N Engl J Med. 2008 Feb 7;358(6):580-91
pubmed: 18256393
J Diabetes Investig. 2018 Mar 2;:
pubmed: 29498232
Rev Diabet Stud. 2009 Spring;6(1):6-12
pubmed: 19557292
N Engl J Med. 1993 Sep 30;329(14):977-86
pubmed: 8366922
J Clin Invest. 1985 Mar;75(3):809-17
pubmed: 3884667
Naunyn Schmiedebergs Arch Pharmacol. 2004 Feb;369(2):151-9
pubmed: 14730417
J Clin Invest. 1974 May;53(5):1441-6
pubmed: 4825234
Acta Biol Med Ger. 1982;41(12):1211-9
pubmed: 6765162
BMJ. 2016 May 03;353:i2231
pubmed: 27142267
J Geriatr Cardiol. 2019 Mar;16(3):291-297
pubmed: 31080472
Lancet. 1998 Sep 12;352(9131):837-53
pubmed: 9742976
Hypertension. 2002 Oct;40(4):458-63
pubmed: 12364347
J Diabetes Investig. 2018 Mar 26;:
pubmed: 29582574
Clin Cardiol. 2014 Aug;37(8):499-504
pubmed: 24895268
J Am Coll Cardiol. 2014 Nov 4;64(18):1929-49
pubmed: 25077860
Am J Hypertens. 1998 Aug;11(8 Pt 1):962-70
pubmed: 9715789
Eur J Gen Pract. 2013 Mar;19(1):17-22
pubmed: 23432037
Diabetes Res Clin Pract. 2018 Apr;138:271-281
pubmed: 29496507
N Engl J Med. 2008 Jun 12;358(24):2545-59
pubmed: 18539917
J Diabetes Investig. 2010 Oct 19;1(5):212-28
pubmed: 24843435
Lancet. 2006 Nov 11;368(9548):1696-705
pubmed: 17098089
BMJ Open. 2018 May 24;8(5):e020852
pubmed: 29794097
Lancet Diabetes Endocrinol. 2017 Dec;5(12):951-964
pubmed: 29079252
Diabetes Obes Metab. 2017 Jun;19(6):800-808
pubmed: 28094466
Ther Adv Endocrinol Metab. 2010 Feb;1(1):23-8
pubmed: 23148146
Blood Press. 2005;14(6):337-44
pubmed: 16403687
Eur J Hum Genet. 2017 Jun;25(7):854-862
pubmed: 28594416
Am J Hypertens. 1995 Apr;8(4 Pt 1):353-7
pubmed: 7619347
Hypertension. 2017 Jul;70(1):42-43
pubmed: 28559390
Endocrinol Diabetes Metab. 2018 Dec 22;2(1):e00053
pubmed: 30815579
J Hypertens. 2007 Jun;25(6):1205-13
pubmed: 17563533
J Clin Med Res. 2015 Apr;7(4):211-9
pubmed: 25699116
Am J Kidney Dis. 2009 Jun;53(6):982-92
pubmed: 19339088
Diabetes Metab J. 2011 Feb;35(1):26-33
pubmed: 21537410
BMJ. 1998 Sep 12;317(7160):703-13
pubmed: 9732337
Drug Saf. 1996 Aug;15(2):135-57
pubmed: 8884164

Auteurs

Tomoyuki Saito (T)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo-Ku, Tokyo, 113-8421 Japan.
Department of Pharmacy, Juntendo University Hospital, 3-1-3 Hongo, Bunkyo-Ku, Tokyo, 113-8431 Japan.

Hirotoshi Ohmura (H)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo-Ku, Tokyo, 113-8421 Japan.

Shuko Nojiri (S)

Juntendo University, Medical Technology Innovation Center, 3-1-3 Hongo, Bunkyo-Ku, Tokyo, 113-8431 Japan.

Hiroyuki Daida (H)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo-Ku, Tokyo, 113-8421 Japan.

Classifications MeSH