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Empagliflozin is associated with lower risk of cardiovascular events and all-cause mortality in routine care in East Asia: Results from the EMPRISE study

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dc.contributor.authorKim, DJ-
dc.contributor.authorSheu, WH-
dc.contributor.authorChung, WJ-
dc.contributor.authorYabe, D-
dc.contributor.authorHa, KH-
dc.contributor.authorNangaku, M-
dc.contributor.authorTan, EC-
dc.contributor.authorNode, K-
dc.contributor.authorYasui, A-
dc.contributor.authorLei, W-
dc.contributor.authorLee, S-
dc.contributor.authorSaarelainen, L-
dc.contributor.authorDeruaz-Luyet, A-
dc.contributor.authorKyaw, MH-
dc.contributor.authorSeino, Y-
dc.contributor.authorEMPRISE East Asia Study Group-
dc.date.accessioned2023-05-04T06:41:46Z-
dc.date.available2023-05-04T06:41:46Z-
dc.date.issued2023-
dc.identifier.issn2040-1116-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/25315-
dc.description.abstractAims/Introduction: The EMPA-REG OUTCOME® trial demonstrated benefits of empagliflozin, a sodium-glucose cotransporter-2 inhibitor (SGLT2i), on cardiovascular, renal outcomes and all-cause mortality in patients with type 2 diabetes and established cardiovascular disease. The EMPRISE study program evaluates how these effects translate in a broad population of patients with type 2 diabetes in routine clinical care across countries. Materials and Methods: The study included patients ≥18 years with type 2 diabetes initiating empagliflozin or any dipeptidyl peptidase-4 inhibitors (DPP-4i) from large administrative databases in Japan, South Korea, and Taiwan. Propensity score-matched (1:1) ‘as-treated’ analyses comparing the risk of cardiovascular outcomes and all-cause mortality between empagliflozin and DPP-4i use were performed in each country. Pooled hazard ratios (pHR) with 95% confidence intervals (CI) were computed using random effects meta-analysis models comparing both empagliflozin and SGLT2i with DPP-4i use, respectively. Intention-to-treat and subgroup analyses in patients with/without cardiovascular disease and in patients receiving 10 mg empagliflozin were performed. Results: The study included 28,712 and 70,233 matched patient pairs for empagliflozin/DPP-4i and SGLT2i/DPP-4i analyses, respectively. The risk of composite outcomes including (i) hospitalization for heart failure (HHF) and all-cause mortality was lower with empagliflozin (pHR 0.76, 95% CI 0.67–0.86) and SGLT2i (0.71, 0.65–0.77); (ii) combined myocardial infarction, stroke, and all-cause mortality was also lower with empagliflozin (0.74, 0.61–0.88) and SGLT2i (0.69, 0.60–0.78) compared to DPP-4i. The intention-to-treat and three subgroup analyses were consistent with results of the main analyses. Conclusions: The results suggest that both empagliflozin and SGLT2i compared with DPP-4i are associated with a lower risk of cardiovascular events and all-cause mortality in routine clinical care in East Asia.-
dc.language.isoen-
dc.subject.MESHAsia, Eastern-
dc.subject.MESHCardiovascular Diseases-
dc.subject.MESHDiabetes Mellitus, Type 2-
dc.subject.MESHDipeptidyl-Peptidase IV Inhibitors-
dc.subject.MESHHumans-
dc.subject.MESHHypoglycemic Agents-
dc.subject.MESHMyocardial Infarction-
dc.subject.MESHSodium-Glucose Transporter 2 Inhibitors-
dc.titleEmpagliflozin is associated with lower risk of cardiovascular events and all-cause mortality in routine care in East Asia: Results from the EMPRISE study-
dc.typeArticle-
dc.identifier.pmid36716212-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951576-
dc.subject.keywordCardiovascular diseases-
dc.subject.keywordObservational study-
dc.subject.keywordSodium-glucose cotransporter 2 inhibitors-
dc.contributor.affiliatedAuthorKim, DJ-
dc.contributor.affiliatedAuthorHa, KH-
dc.type.localJournal Papers-
dc.identifier.doi10.1111/jdi.13959-
dc.citation.titleJournal of diabetes investigation-
dc.citation.volume14-
dc.citation.number3-
dc.citation.date2023-
dc.citation.startPage417-
dc.citation.endPage428-
dc.identifier.bibliographicCitationJournal of diabetes investigation, 14(3). : 417-428, 2023-
dc.identifier.eissn2040-1124-
dc.relation.journalidJ020401116-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Endocrinology & Metabolism
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