Empagliflozin and Cardiovascular Outcomes in Asian Patients With Type 2 Diabetes and Established Cardiovascular Disease - Results From EMPA-REG OUTCOME®

被引:111
作者
Kaku, Kohei [1 ]
Lee, Jisoo [2 ]
Mattheus, Michaela [2 ]
Kaspers, Stefan [2 ]
George, Jyothis [3 ]
Woerle, Hans-Juergen [2 ]
Aizenberg, D. [4 ]
Ulla, M. [5 ]
Waitman, J. [6 ]
De Loredo, L. [7 ,8 ]
Farias, J. [9 ]
Fideleff, H. [9 ]
Lagrutta, M. [10 ]
Maldonado, N. [11 ]
Colombo, H. [12 ]
Ferre Pacora, F. [13 ]
Wasserman, A. [14 ]
Maffei, L. [15 ]
Lehman, R. [16 ]
Selvanayagam, J. [17 ]
d'Emden, M. [18 ]
Fasching, P. [19 ]
Paulweber, B. [20 ]
Toplak, H. [21 ]
Luger, A. [22 ]
Drexel, H. [23 ]
Prager, R. [24 ]
Schnack, C. [25 ]
Schernthaner, G. [25 ,26 ]
Fliesser-Goerzer, E.
Kaser, S. [27 ]
Scheen, A. [28 ]
Van Gaal, L. [29 ]
Hollanders, G.
Kockaerts, Y. [30 ]
Capiau, L.
Chachati, A. [31 ]
Persu, A. [32 ]
Hermans, M. [32 ]
Vantroyen, D. [33 ]
Vercammen, C. [34 ]
Van de Borne, P. [35 ]
Mathieu, C. [36 ]
Benhalima, K. [36 ]
Lienart, F. [37 ]
Mortelmans, J.
Strivay, M. [38 ]
Vereecken, G.
Keymeulen, B. [39 ]
Lamkanfi, F. [39 ]
机构
[1] Kawasaki Med Sch, Dept Gen Internal Med, 577 Matsushima, Kurashiki, Okayama 7010192, Japan
[2] Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany
[3] Boehringer Ingelheim Ltd, Bracknell, Berks, England
[4] Ctr Med Viamonte, Buenos Aires, DF, Argentina
[5] ILAIMCEOM, Cordoba, Cba, Argentina
[6] Ctr Diabetol Dr Waitman, Cordoba, Cba, Argentina
[7] Hosp Privado Ctr Med Cordoba SA, Cordoba, Cba, Argentina
[8] Parque Velez Sarfield, Cordoba, Cba, Argentina
[9] Sanatorio Guemes Hosp Privado, Buenos Aires, DF, Argentina
[10] Inst Invest Clin, Rosario, Santa Fe, Argentina
[11] Ctr Med Alta Complejidad, Rosario, Santa Fe, Argentina
[12] Clin Privada Colombo, Cordoba, Co, Argentina
[13] Ctr Med Colon, Cordoba, Co, Argentina
[14] Fepreva, Buenos Aires, DF, Argentina
[15] Consultorios Asociados Endocrinol & Invest Clin, Buenos Aires, DF, Argentina
[16] Adelaide Med Res, Ashford, SA, Australia
[17] Heart & Vasc Inst, Fullarton, SA, Australia
[18] Royal Brisbane & Womens Hosp, Herston, Qld, Australia
[19] Wilhelminenspital Wien, Vienna, Austria
[20] LKH Salzburg, St Johanns Spital, Salzburg, Austria
[21] Med Univ Graz, Graz, Austria
[22] Univ Klin Innere Med III, Vienna, Austria
[23] Landeskrankenhaus Feldkirch, Feldkirch, Austria
[24] Krankenhaus Hietzing NZR, Vienna, Austria
[25] Krankenanstalt Rudolfstiftung Wien, Semmelweis Frauenklin, Vienna, Austria
[26] Univ Klin Innere Med II, Vienna, Austria
[27] Univ Klin Innsbruck, Innsbruck, Austria
[28] Ctr Hosp Univ Liege, Liege, Belgium
[29] UZA, Edegem, Belgium
[30] Ziekenhuis Oost Limburg, Genk, Belgium
[31] CHR Huy, Huy, Belgium
[32] Clin Univ St Luc, Brussels, Belgium
[33] Huisartsenpraktijk Hygeia, Hasselt, Belgium
[34] Imelda ZH Bonheiden, Bonheiden, Belgium
[35] Hop Univ Erasme, Brussels, Belgium
[36] Univ Hosp Gasthuisberg, Leuven, Belgium
[37] CHU Tivoli, La Louviere, Belgium
[38] CHR Citadelle, Site Citadelle, Liege, Belgium
[39] UZ Brussels, Brussels, Belgium
[40] Hosp Sao Paulo UNIFESP, Villa Clementino, SP, Brazil
[41] Ctr Pesquisas Clin Ltda, Higienopolis, SP, Brazil
[42] Hosp Rim Hipertensao, Vila Clementino, SP, Brazil
[43] Inst Dante Pazzanese Cardiol, Sao Paulo, Brazil
[44] Blumenau Serv Med SC Ltda, Vila Leopoldina, SP, Brazil
[45] Irmandade Santa Casa Misericordia Sao Paulo, Vila Albuquerque, SP, Brazil
[46] Hosp Guilherme Alvaro, Ctr Pesquisas Clin, Boqueirao, ST, Brazil
[47] Hosp Mae Deus, Porto Alegre, RS, Brazil
[48] Hosp Geral Goiania, Goiania, Go, Brazil
[49] FMUSP, Hosp Clin Sao Paulo, Sao Paulo, Brazil
[50] Univ Ribeirao Preto, Hosp Elect Bonini, Ribeirao Preto, Brazil
关键词
Diabetes mellitus; Mortality; Race; Sodium-glucose cotransporter 2; Treatment outcomes; INHIBITION;
D O I
10.1253/circj.CJ-16-1148
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In the EMPA-REG OUTCOME (R) trial, empagliflozin added to standard of care reduced the risk of 3-point major adverse cardiovascular (CV) events (3-point MACE: composite of CV death, non-fatal myocardial infarction, or non-fatal stroke) by 14%, CV death by 38%, hospitalization for heart failure by 35%, and all-cause mortality by 32% in patients with type 2 diabetes (T2DM) and established CV disease. We investigated the effects of empagliflozin in patients of Asian race. Methods and Results: Patients were randomized to receive empagliflozin 10 mg, empagliflozin 25 mg, or placebo. Of 7,020 patients treated, 1,517 (21.6%) were of Asian race. The reduction in 3-point MACE in Asian patients was consistent with the overall population: 3-point MACE occurred in 79/1,006 patients (7.9%) in the pooled empagliflozin group vs. 58/511 patients (11.4%) in the placebo group (hazard ratio: 0.68 [95% confidence interval: 0.48-0.95], P-value for treatment by race interaction (Asian, White, Black/African-American): 0.0872). The effects of empagliflozin on the components of MACE, all-cause mortality, and heart failure outcomes in Asian patients were consistent with the overall population (P-values for interaction by race >0.05). The adverse event profile of empagliflozin in Asian patients was similar to the overall trial population. Conclusions: Reductions in the risk of CV outcomes and mortality with empagliflozin in Asian patients with T2DM and established CV disease were consistent with the overall trial population.
引用
收藏
页码:227 / +
页数:11
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