Evidence map›Paper›PMID 36716212›Full record

SynthesisJournal of diabetes investigation2023

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

Dae Jung Kim, Wayne H-H Sheu, Wook-Jin Chung, Daisuke Yabe, Kyoung Hwa Ha, Masaomi Nangaku, Elise Chia-Hui Tan, Koichi Node, Atsutaka Yasui, Weiyu Lei and 6 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Journal of diabetes investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Article
  3. Protective Mechanisms of SGLTi in Ischemic Heart Disease.Journal of cardiovascular translational research · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 15 institutions in 8 countries.

Dae Jung KimDepartment of Endocrinology and Metabolism, Ajou University School of Medicine, Suwon, South Korea.ORCID https://orcid.org/0000-0003-1025-2044
Wayne H-H SheuDivision of Endocrinology and Metabolism, Taipei Veterans General Hospital, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-8805-8340
Wook-Jin ChungDepartment of Cardiovascular Medicine, Gachon University Gil Medical Center, Incheon, South Korea.
Daisuke YabeKansai Electric Power Medical Research Institute, Kobe, Japan.ORCID https://orcid.org/0000-0002-5334-7687
Kyoung Hwa HaDepartment of Endocrinology and Metabolism, Ajou University School of Medicine, Suwon, South Korea.
Masaomi NangakuDivision of Nephrology and Endocrinology, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0001-7401-2934
Elise Chia-Hui TanNational Research Institute of Chinese Medicine, Ministry of Health and Welfare, Taipei, Taiwan.
Koichi NodeDepartment of Cardiovascular Medicine, Saga University, Saga, Japan.ORCID https://orcid.org/0000-0002-2534-0939
Atsutaka YasuiNippon Boehringer Ingelheim Co. Ltd, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4903-7210
Weiyu LeiBoehringer Ingelheim Taiwan Ltd, Taipei, Taiwan.
Sunwoo LeeBoehringer Ingelheim Korea Ltd, Seoul, South Korea.
Laura SaarelainenIQVIA, Espoo, Finland.
Anouk Deruaz-LuyetBoehringer Ingelheim International GmbH, Ingelheim, Germany.
Moe H KyawBoehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut, USA.
Yutaka SeinoKansai Electric Power Medical Research Institute, Kobe, Japan.ORCID https://orcid.org/0000-0002-1099-7989
EMPRISE East Asia Study Group
Ajou University · KRBoehringer Ingelheim (Germany) · DEBoehringer Ingelheim (Japan) · JPBoehringer Ingelheim (South Korea) · KRBoehringer Ingelheim (Taiwan) · TWBoehringer Ingelheim (United States) · USGachon University Gil Medical Center · KRIQM (Finland) · FIKansai Electric Power (Japan) · JPNational Yang Ming Chiao Tung University · TWSaga University · JPTaipei Veterans General Hospital · TWThe University of Tokyo · JPTiGenix (Spain) · ESTokai Gakuen University · JP

Funding

BI Lilly Alliance
6 · The paper itself

Abstract

AIMS/

introductionThe 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

methodsThe 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.

resultsThe 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.

conclusionsThe 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.

Indexed as

Cardiovascular DiseasesDiabetes Mellitus, Type 2Dipeptidyl-Peptidase IV InhibitorsMyocardial InfarctionSodium-Glucose Transporter 2 InhibitorsAsia, EasternBenzhydryl CompoundsGlucosidesHumansHypoglycemic AgentsBenzhydryl CompoundsDipeptidyl-Peptidase IV InhibitorsempagliflozinGlucosidesHypoglycemic AgentsSodium-Glucose Transporter 2 InhibitorsCardiovascular diseasesObservational studySodium-glucose cotransporter 2 inhibitors

Identifiers

PMID36716212
PMCPMC9951576
OpenAlexW4318542298

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.