Empagliflozin Use Is Associated With Lower Risk of All-Cause Mortality, Hospitalization for Heart Failure, and End-Stage Renal Disease Compared to DPP-4i in Nordic Type 2 Diabetes Patients: Results From the EMPRISE (Empagliflozin Comparative Effectiveness and Safety) Study

被引:0
作者
Langslet, Gisle [1 ]
Nystroem, Thomas [2 ]
Vistisen, Dorte [3 ,4 ]
Carstensen, Bendix [3 ]
Grip, Emilie Toresson [5 ,6 ]
Casajust, Paula [7 ]
Tskhvarashvili, Giorgi [8 ]
Hoti, Fabian [9 ]
Klement, Riho [10 ]
Karlsdotter, Kristina [11 ]
Tuovinen, Mikko [12 ]
Ofstad, Anne Pernille [13 ,14 ]
Lajer, Maria [15 ]
Shay, Christina [16 ]
Koeneman, Lisette [17 ]
Farsani, Soulmaz Fazeli [18 ]
Niskanen, Leo [19 ,20 ]
Halvorsen, Sigrun [21 ,22 ]
机构
[1] Oslo Univ Hosp, Dept Endocrinol Morbid Obes & Prevent Med, Lipid Clin, N-0424 Oslo, Norway
[2] Karolinska Inst, Dept Clin Sci & Educ, Sodersjukhuset, S-11883 Stockholm, Sweden
[3] Steno Diabet Ctr Copenhagen, Clin Epidemiol, DK-2730 Herlev, Denmark
[4] Novo Nordisk AS, AI & Analyt, Soborg, Denmark
[5] Quantify Res, Real World Data & Data Analyt, S-11221 Stockholm, Sweden
[6] Karolinska Inst, Dept Med, S-14157 Huddinge, Sweden
[7] TFS HealthSci, Real World Data & Data Analyt, Barcelona 08007, Spain
[8] IQVIA, Global Database Studies, Real World Solut, EE-10119 Tallinn, Estonia
[9] IQVIA, Global Database Studies, Real World Solut, Espoo, Finland
[10] IQVIA, Global Database Studies, Real World Solut, Tartu, Estonia
[11] Boehringer Ingelheim Pharmaceut, Market Access, Stockholm, Sweden
[12] Boehringer Ingelheim Pharmaceut, Global Med Affairs, Helsinki, Finland
[13] Boehringer Ingelheim GmbH & Co KG, Med Dept, Type 2 Diabet & Metab, Oslo, KS, Norway
[14] Oslo Diabet Res Ctr, Oslo, Norway
[15] Boehringer Ingelheim Pharmaceut, Global Integrated Evidence, DK-2100 Copenhagen, Denmark
[16] Boehringer Ingelheim Pharmaceut Inc, Global Integrated Evidence, Ridgefield, CT 06877 USA
[17] Lilly Deutschland GmbH, Diabet Global Med Affairs, D-61352 Bad Ingelheim, Germany
[18] Boehringer Ingelheim Int GmbH, Global RWE Capabil, Ingelheim, Germany
[19] Paijat Hame Cent Hosp, Paijat Hame Joint Author Hlth & Wellbeing, Lahti, Finland
[20] Univ Eastern Finland, Inst Clin Med, Kuopio 70210, Finland
[21] Oslo Univ Hosp Ulleval, Dept Cardiol, N-0450 Oslo, Norway
[22] Univ Oslo, Inst Clin Med, Oslo, Norway
关键词
cardiovascular diseases; comparative effectiveness; dipeptidyl peptidase-4 inhibitors; empagliflozin; end-stage renal disease; heart failure; sodium-glucose cotransporter-2 inhibitors; type 2 diabetes mellitus; CARDIOVASCULAR OUTCOMES; CVD-REAL; INHIBITORS; DRUGS;
D O I
10.1155/2024/6142211
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate the effectiveness of empagliflozin in reducing all-cause mortality (ACM), hospitalization for heart failure (HHF), myocardial infarction (MI), stroke, cardiovascular mortality (CVM), and end-stage renal disease (ESRD) in routine clinical practice in the Nordic countries of the Empagliflozin Comparative Effectiveness and Safety (EMPRISE) study.Methods: This noninterventional, multicountry cohort study used secondary data from four Nordic countries (Denmark, Sweden, Finland, and Norway). Propensity score (PS) matched (1:1) adults with type 2 diabetes (T2D) initiating empagliflozin (a sodium-glucose cotransporter-2 inhibitor) during 2014-2018 who were compared to those initiating a dipeptidyl peptidase-4 inhibitor (DPP-4i). Cox proportional hazards regression modelling was used to assess the risk for ACM, HHF, MI, stroke, CVM, and ESRD. Meta-analyses were conducted and hazard ratios (HRs) with 95% confidence intervals (CIs) from random-effects models were calculated.Results: A total of 43,695 pairs of PS-matched patients were identified. Patients initiating empagliflozin exhibited a 49% significantly lower risk of ACM (HR: 0.51, 95% CI 0.40-0.64) compared to DPP-4i. Additionally, empagliflozin was associated with a 36% significantly lower risk of HHF (HR: 0.64, 95% CI 0.46-0.89), a 52% significantly lower risk of CVM (HR: 0.48, 95% CI 0.37-0.63), and a 66% significantly lower risk of ESRD (HR: 0.34, 95% CI 0.15-0.77) compared to DPP-4i. No significant differences were observed in the risk of stroke and MI between patients initiating empagliflozin compared with those initiating a DPP-4i. Results were generally consistent for subgroups (with/without pre-existing CV disease or congestive heart failure) and in sensitivity analyses.Conclusion: Empagliflozin initiation was associated with a significantly reduced risk of ACM, HHF, CVM, and ESRD compared with initiation of DPP-4i in patients with T2D when examining routine clinical practice data from Nordic countries.
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页数:22
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