Sodium-glucose cotransporter 2 inhibitors compared with other glucose-lowering drugs in Japan: Subanalyses of the CVD-REAL 2 Study.
Biomarkers
/ analysis
Blood Glucose
/ analysis
Cardiovascular Diseases
/ chemically induced
Diabetes Mellitus, Type 2
/ complications
Dipeptidyl-Peptidase IV Inhibitors
/ administration & dosage
Female
Follow-Up Studies
Glycated Hemoglobin
/ analysis
Humans
Hypoglycemic Agents
/ administration & dosage
Male
Middle Aged
Prognosis
Retrospective Studies
Risk Factors
Sodium-Glucose Transporter 2 Inhibitors
/ administration & dosage
Cardiovascular event
Sodium-glucose cotransporter 2
Type 2 diabetes
Journal
Journal of diabetes investigation
ISSN: 2040-1124
Titre abrégé: J Diabetes Investig
Pays: Japan
ID NLM: 101520702
Informations de publication
Date de publication:
Jan 2021
Jan 2021
Historique:
received:
16
01
2020
revised:
21
05
2020
accepted:
04
06
2020
pubmed:
13
6
2020
medline:
5
10
2021
entrez:
13
6
2020
Statut:
ppublish
Résumé
There are limited data on cardiovascular efficacy and safety of type 2 diabetes therapies in Japan, where treatments are characterized by lower metformin use and higher dipeptidyl peptidase-4 inhibitor (DPP4i) use versus other countries. We investigated the cardiovascular outcomes in Japanese patients with type 2 diabetes initiating sodium-glucose cotransporter 2 inhibitors (SGLT2i) matched 1:1 to patients initiating other glucose-lowering drugs (33,890 patients/group) or DPP4i (9,876 patients/group). SGLT2i initiation was associated with lower risks (hazard ratio of in-hospital death [death] 0.56, 95% confidence interval [CI] 0.47-0.67; hospitalization for heart failure 0.75, 95% CI 0.64-0.89; composite of hospitalization for heart failure or death 0.65, 95% CI 0.58-0.74 and stroke 0.66, 95% CI 0.52-0.84 versus other glucose-lowering drugs and lower risks of death 0.52, 95% CI 0.36-0.73) and composite of hospitalization for heart failure or death (0.65, 95% CI 0.51-0.83) versus DPP4i. In conclusion, SGLT2i initiators had lower risks of cardiovascular events versus other glucose-lowering drug initiators and, uniquely, versus DPP4i initiators in Japanese real-world practice.
Identifiants
pubmed: 32530554
doi: 10.1111/jdi.13321
pmc: PMC7779275
doi:
Substances chimiques
Biomarkers
0
Blood Glucose
0
Dipeptidyl-Peptidase IV Inhibitors
0
Glycated Hemoglobin A
0
Hypoglycemic Agents
0
Sodium-Glucose Transporter 2 Inhibitors
0
hemoglobin A1c protein, human
0
Types de publication
Comparative Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
67-73Subventions
Organisme : AstraZeneca
Informations de copyright
© 2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.
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