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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
DC Field | Value | Language |
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dc.contributor.author | Kim, DJ | - |
dc.contributor.author | Sheu, WH | - |
dc.contributor.author | Chung, WJ | - |
dc.contributor.author | Yabe, D | - |
dc.contributor.author | Ha, KH | - |
dc.contributor.author | Nangaku, M | - |
dc.contributor.author | Tan, EC | - |
dc.contributor.author | Node, K | - |
dc.contributor.author | Yasui, A | - |
dc.contributor.author | Lei, W | - |
dc.contributor.author | Lee, S | - |
dc.contributor.author | Saarelainen, L | - |
dc.contributor.author | Deruaz-Luyet, A | - |
dc.contributor.author | Kyaw, MH | - |
dc.contributor.author | Seino, Y | - |
dc.contributor.author | EMPRISE East Asia Study Group | - |
dc.date.accessioned | 2023-05-04T06:41:46Z | - |
dc.date.available | 2023-05-04T06:41:46Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 2040-1116 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/25315 | - |
dc.description.abstract | Aims/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.iso | en | - |
dc.subject.MESH | Asia, Eastern | - |
dc.subject.MESH | Cardiovascular Diseases | - |
dc.subject.MESH | Diabetes Mellitus, Type 2 | - |
dc.subject.MESH | Dipeptidyl-Peptidase IV Inhibitors | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Hypoglycemic Agents | - |
dc.subject.MESH | Myocardial Infarction | - |
dc.subject.MESH | Sodium-Glucose Transporter 2 Inhibitors | - |
dc.title | Empagliflozin is associated with lower risk of cardiovascular events and all-cause mortality in routine care in East Asia: Results from the EMPRISE study | - |
dc.type | Article | - |
dc.identifier.pmid | 36716212 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951576 | - |
dc.subject.keyword | Cardiovascular diseases | - |
dc.subject.keyword | Observational study | - |
dc.subject.keyword | Sodium-glucose cotransporter 2 inhibitors | - |
dc.contributor.affiliatedAuthor | Kim, DJ | - |
dc.contributor.affiliatedAuthor | Ha, KH | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1111/jdi.13959 | - |
dc.citation.title | Journal of diabetes investigation | - |
dc.citation.volume | 14 | - |
dc.citation.number | 3 | - |
dc.citation.date | 2023 | - |
dc.citation.startPage | 417 | - |
dc.citation.endPage | 428 | - |
dc.identifier.bibliographicCitation | Journal of diabetes investigation, 14(3). : 417-428, 2023 | - |
dc.identifier.eissn | 2040-1124 | - |
dc.relation.journalid | J020401116 | - |
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