Cardiovascular Events Associated With SGLT-2 Inhibitors Versus Other Glucose-Lowering Drugs

Mikhail Kosiborod(Saint Luke's Hospital), Mikhail Kosiborod(University Medical Center Groningen), Carolyn S.P. Lam(University Medical Center Groningen), Shun Kohsaka(Keio University), Dae Jung Kim(Tel Aviv University), Avraham Karasik(Baker Heart and Diabetes Institute), Jonathan E. Shaw(Baker Heart and Diabetes Institute), Navdeep Tangri(Singapore General Hospital), Su‐Yen Goh(Singapore General Hospital), Marcus Thuresson(AstraZeneca (United States)), Hungta Chen(AstraZeneca (United Kingdom)), Filip Surmont(AstraZeneca (United Kingdom)), Niklas Hammar(AstraZeneca (United Kingdom)), Peter Fenici(AstraZeneca (United Kingdom)), Mikhail Kosiborod(Saint Luke's Hospital), Mikhail Kosiborod(Saint Luke's Hospital), Matthew A. Cavender, Alex Z. Fu, John Wilding, Kamlesh Khunti, Anna Norhammar, Kåre I. Birkeland, Marit E. Jørgensen(University Medical Center Groningen), Reinhard W. Holl, Carolyn S.P. Lam(University Medical Center Groningen), Hanne Løvdal Gulseth, Bendix Carstensen, Esther Bollow, Josep Franch‐Nadal(Tel Aviv University), Luis A. Garcı́a Rodrı́guez(University of Manitoba), Avraham Karasik(Tel Aviv University), Navdeep Tangri(University of Manitoba), Shun Kohsaka(Baker Heart and Diabetes Institute), Dae Jung Kim(Ajou University), Jonathan E. Shaw(Baker Heart and Diabetes Institute), Suzanne V. Arnold(Karolinska Institutet), Su‐Yen Goh(AstraZeneca (United Kingdom)), Niklas Hammar(Karolinska Institutet), Peter Fenici(AstraZeneca (United Kingdom)), Johan Bodegård(AstraZeneca (United Kingdom)), Hungta Chen(AstraZeneca (United States)), Filip Surmont(AstraZeneca (United Kingdom)), Kyle Nahrebne, Betina T. Blak, Eric Wittbrodt, Matthias Saathoff(University of Manitoba), Yusuke Noguchi, Donna Tan, Maro R. I. Williams, Hye Won Lee, Maya Greenbloom, Oksana Kaidanovich‐Beilin, Khung Keong Yeo, Yong Mong Bee, Joan Khoo, Agnes Koong, Yee How Lau(University of Manitoba), Fei Gao, Wee Boon Tan(Karolinska Institutet), Hanis Abdul Kadir, Kyoung Hwa Ha, Jinhee Lee, Gabriel Chodick, Cheli Melzer Cohen, Reid Whitlock, Lucía Cea Soriano, Oscar Fernández Cantero, Ellen Riehle, Jenni Ilomäki, Dianna J. Magliano
Journal of the American College of Cardiology
March 14, 2018
Cited by 464Open Access
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Abstract

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. 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. 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. 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. 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. (Comparative Effectiveness of Cardiovascular Outcomes in New Users of SGLT-2 Inhibitors [CVD-REAL]; NCT02993614)


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