TY - JOUR
T1 - Cardiovascular Events Associated With SGLT-2 Inhibitors Versus Other Glucose-Lowering Drugs
T2 - The CVD-REAL 2 Study
AU - CVD-REAL Investigators and Study Group
AU - Kosiborod, Mikhail
AU - Lam, Carolyn S.P.
AU - Kohsaka, Shun
AU - Kim, Dae Jung
AU - Karasik, Avraham
AU - Shaw, Jonathan
AU - Tangri, Navdeep
AU - Goh, Su Yen
AU - Thuresson, Marcus
AU - Chen, Hungta
AU - Surmont, Filip
AU - Hammar, Niklas
AU - Fenici, Peter
AU - Cavender, Matthew A.
AU - Fu, Alex Z.
AU - Wilding, John P.
AU - Khunti, Kamlesh
AU - Norhammar, Anna
AU - Birkeland, Kåre
AU - Jørgensen, Marit Eika
AU - Holl, Reinhard W.
AU - Gulseth, Hanne Løvdal
AU - Carstensen, Bendix
AU - Bollow, Esther
AU - Franch-Nadal, Josep
AU - García Rodríguez, Luis Alberto
AU - Karasik, Avraham
AU - Tangri, Navdeep
AU - Kohsaka, Shun
AU - Kim, Dae Jung
AU - Arnold, Suzanne
AU - Goh, Su Yen
AU - Hammar, Niklas
AU - Fenici, Peter
AU - Bodegård, Johan
AU - Chen, Hungta
AU - Surmont, Filip
AU - Nahrebne, Kyle
AU - Blak, Betina T.
AU - Wittbrodt, Eric T.
AU - Saathoff, Matthias
AU - Noguchi, Yusuke
AU - Tan, Donna
AU - Williams, Maro
AU - Lee, Hye Won
AU - Greenbloom, Maya
AU - Kaidanovich-Beilin, Oksana
AU - Yeo, Khung Keong
AU - Bee, Yong Mong
AU - Khoo, Joan
N1 - Funding Information:
This study was funded by AstraZeneca. Dr. Kosiborod has received research grants from AstraZeneca and Boehringer Ingelheim; has served on advisory boards for AstraZeneca, Boehringer Ingelheim, Amgen, Sanofi, Glytec, Novo Nordisk, ZS Pharma, Janssen, Merck (Diabetes), and Novartis; and has served as a consultant for AstraZeneca, Boehringer Ingelheim, Sanofi, GlaxoSmithKline, Janssen, Intarcia, Merck (Diabetes), Novo Nordisk, Glytec, and ZS Pharma. Dr. Lam has received research support from Boston Scientific, Bayer, Thermo Fisher, Medtronic, and Vifor Pharma; and has consulted for Bayer, Novartis, Takeda, Merck, AstraZeneca, Janssen Research & Development, Menarini, Boehringer Ingelheim, Abbott Diagnostics, Corvia, Stealth BioTherapeutics, Roche, and Amgen. Dr. Kohsaka has received grants from Bayer Yakuhin and Daiichi-Sankyo; has received lecture fees from Bayer Yakuhin and Bristol-Myers Squibb; and has received consulting fees from Pfizer. Dr. Kim has received grant support from LG Life Sciences, Chong Kun Dang, and AstraZeneca; has been a consultant for AstraZeneca, Novo Nordisk, and Sanofi; and has received speaker fees from Novo Nordisk, Takeda, Handok, CJ Healthcare, Chong Kun Dang, Merck Sharp and Dohme, Hanmi, and AstraZeneca. Dr. Karasik has received grants and consulting fees from AstraZeneca, Novo Nordisk, Merck, and Boehringer Ingelheim. Dr. Shaw has received honoraria for consulting and lectures from AstraZeneca, Boehringer Ingelheim, Eli Lilly, Merck Sharp and Dohme, Mylan, Novartis, Novo Nordisk, and Sanofi. Dr. Tangri has received consulting fees from Otsuka, Tricida, and AstraZeneca; has received research support from AstraZeneca, including for this work; and his research program is supported by the Canadian Institute for Health Research and Research Manitoba. Dr. Goh has received institutional grants from AstraZeneca, Medtronic, and Sanofi; and has received honoraria for participation in advisory boards for Amgen, AstraZeneca, Boehringer Ingelheim, Novo Nordisk, Medtronic, and Sanofi. Dr. Thuresson is an employee at Statisticon, for which AstraZeneca is a client; and has served as a statistical consultant for AstraZeneca. Drs. Chen, Surmont, Hammar, and Fenici are AstraZeneca employees. Dr. Fenici owns stock options in AstraZeneca.
Funding Information:
The authors thank Kevin Kennedy from Saint Luke's Mid America for his independent validation of the data and Nicola Truss, PhD, from inScience Communications, Springer Healthcare, for editorial support (funded by AstraZeneca).
Publisher Copyright:
© 2018 The Authors
PY - 2018/6/12
Y1 - 2018/6/12
N2 - Background: Randomized trials demonstrated a lower risk of cardiovascular (CV) events with sodium-glucose cotransporter-2 inhibitors (SGLT-2i) in patients with type 2 diabetes (T2D) at high CV risk. Prior real-world data suggested similar SGLT-2i effects in T2D patients with a broader risk profile, but these studies focused on heart failure and death and were limited to the United States and Europe. Objectives: The purpose of this study was to examine a broad range of CV outcomes in patients initiated on SGLT-2i versus other glucose-lowering drugs (oGLDs) across 6 countries in the Asia Pacific, the Middle East, and North American regions. Methods: New users of SGLT-2i and oGLDs were identified via claims, medical records, and national registries in South Korea, Japan, Singapore, Israel, Australia, and Canada. Propensity scores for SGLT-2i initiation were developed in each country, with 1:1 matching. Hazard ratios (HRs) for death, hospitalization for heart failure (HHF), death or HHF, MI, and stroke were assessed by country and pooled using weighted meta-analysis. Results: After propensity-matching, there were 235,064 episodes of treatment initiation in each group; ∼27% had established CV disease. Patient characteristics were well-balanced between groups. Dapagliflozin, empagliflozin, ipragliflozin, canagliflozin, tofogliflozin, and luseogliflozin accounted for 75%, 9%, 8%, 4%, 3%, and 1% of exposure time in the SGLT-2i group, respectively. Use of SGLT-2i versus oGLDs was associated with a lower risk of death (HR: 0.51; 95% confidence interval [CI]: 0.37 to 0.70; p < 0.001), HHF (HR: 0.64; 95% CI: 0.50 to 0.82; p = 0.001), death or HHF (HR: 0.60; 95% CI: 0.47 to 0.76; p < 0.001), MI (HR: 0.81; 95% CI: 0.74 to 0.88; p < 0.001), and stroke (HR: 0.68; 95% CI: 0.55 to 0.84; p < 0.001). Results were directionally consistent across both countries and patient subgroups, including those with and without CV disease. Conclusions: In this large, international study of patients with T2D from the Asia Pacific, the Middle East, and North America, initiation of SGLT-2i was associated with a lower risk of CV events across a broad range of outcomes and patient characteristics.
AB - Background: Randomized trials demonstrated a lower risk of cardiovascular (CV) events with sodium-glucose cotransporter-2 inhibitors (SGLT-2i) in patients with type 2 diabetes (T2D) at high CV risk. Prior real-world data suggested similar SGLT-2i effects in T2D patients with a broader risk profile, but these studies focused on heart failure and death and were limited to the United States and Europe. Objectives: The purpose of this study was to examine a broad range of CV outcomes in patients initiated on SGLT-2i versus other glucose-lowering drugs (oGLDs) across 6 countries in the Asia Pacific, the Middle East, and North American regions. Methods: New users of SGLT-2i and oGLDs were identified via claims, medical records, and national registries in South Korea, Japan, Singapore, Israel, Australia, and Canada. Propensity scores for SGLT-2i initiation were developed in each country, with 1:1 matching. Hazard ratios (HRs) for death, hospitalization for heart failure (HHF), death or HHF, MI, and stroke were assessed by country and pooled using weighted meta-analysis. Results: After propensity-matching, there were 235,064 episodes of treatment initiation in each group; ∼27% had established CV disease. Patient characteristics were well-balanced between groups. Dapagliflozin, empagliflozin, ipragliflozin, canagliflozin, tofogliflozin, and luseogliflozin accounted for 75%, 9%, 8%, 4%, 3%, and 1% of exposure time in the SGLT-2i group, respectively. Use of SGLT-2i versus oGLDs was associated with a lower risk of death (HR: 0.51; 95% confidence interval [CI]: 0.37 to 0.70; p < 0.001), HHF (HR: 0.64; 95% CI: 0.50 to 0.82; p = 0.001), death or HHF (HR: 0.60; 95% CI: 0.47 to 0.76; p < 0.001), MI (HR: 0.81; 95% CI: 0.74 to 0.88; p < 0.001), and stroke (HR: 0.68; 95% CI: 0.55 to 0.84; p < 0.001). Results were directionally consistent across both countries and patient subgroups, including those with and without CV disease. Conclusions: In this large, international study of patients with T2D from the Asia Pacific, the Middle East, and North America, initiation of SGLT-2i was associated with a lower risk of CV events across a broad range of outcomes and patient characteristics.
KW - SGLT-2 inhibitor
KW - death
KW - diabetes mellitus
KW - heart failure
KW - observational studies
KW - sodium glucose cotransporter-2 inhibitors
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UR - http://www.scopus.com/inward/citedby.url?scp=85047499725&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2018.03.009
DO - 10.1016/j.jacc.2018.03.009
M3 - Article
C2 - 29540325
AN - SCOPUS:85047499725
SN - 0735-1097
VL - 71
SP - 2628
EP - 2639
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 23
ER -