TY - JOUR
T1 - Cardiovascular outcomes with sodium–glucose cotransporter-2 inhibitors vs other glucose-lowering drugs in 13 countries across three continents
T2 - analysis of CVD-REAL data
AU - the CVD-REAL Investigators and Study Group
AU - Khunti, Kamlesh
AU - Kosiborod, Mikhail
AU - Kim, Dae Jung
AU - Kohsaka, Shun
AU - Lam, Carolyn S.P.
AU - Goh, Su Yen
AU - Chiang, Chern En
AU - Shaw, Jonathan E.
AU - Cavender, Matthew A.
AU - Tangri, Navdeep
AU - Franch-Nadal, Josep
AU - Holl, Reinhard W.
AU - Jørgensen, Marit E.
AU - Norhammar, Anna
AU - Eriksson, Johan G.
AU - Zaccardi, Francesco
AU - Magliano, Dianna J.
AU - Thuresson, Marcus
AU - Chen, Hungta
AU - Wittbrodt, Eric
AU - Bodegård, Johan
AU - Surmont, Filip
AU - Fenici, Peter
AU - Kosiborod, Mikhail
AU - Cavender, Matthew A.
AU - Wilding, John P.
AU - Birkeland, Kåre
AU - Norhammar, Anna
AU - Carstensen, Bendix
AU - Jørgensen, Marit Eika
AU - Holl, Reinhard W.
AU - Lam, Carolyn S.P.
AU - Kendrick, Rachel
AU - Belli, Wesley
AU - Wittbrodt, Eric T.
AU - Franch-Nadal, Josep
AU - Noguchi, Yusuke
AU - Karasik, Avraham
AU - Tangri, Navdeep
AU - Kohsaka, Shun
AU - Kim, Dae Jung
AU - Shaw, Jonathan
AU - Andersson-Sundell, Karolina
AU - Goh, Su Yen
AU - Chiang, Chern En
AU - Eriksson, Johan G.
AU - Zaccardi, Francesco
AU - Fenici, Peter
AU - Bodegård, Johan
N1 - Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - Background: Randomized, controlled cardiovascular outcome trials may not be fully representative of the management of patients with type 2 diabetes across different geographic regions. We conducted analyses of data from the multinational CVD-REAL consortium to determine the association between initiation of sodium–glucose cotransporter-2 inhibitors (SGLT-2i) and cardiovascular outcomes, including subgroup analyses based on patient characteristics. Methods: De-identified health records from 13 countries across three continents were used to identify patients newly-initiated on SGLT-2i or other glucose-lowering drugs (oGLDs). Propensity scores for SGLT-2i initiation were developed in each country, with 1:1 matching for oGLD initiation. In the matched groups hazard ratios (HRs) for hospitalization for heart failure (HHF), all-cause death (ACD), the composite of HHF or ACD, myocardial infarction (MI) and stroke were estimated by country, and pooled using a weighted meta-analysis. Multiple subgroup analyses were conducted across patient demographic and clinical characteristics to examine any heterogeneity in treatment effects. Results: Following matching, 440,599 new users of SGLT-2i and oGLDs were included in each group. Mean follow-up time was 396 days for SGLT-2i initiation and 406 days for oGLDs initiation. SGLT-2i initiation was associated with a lower risk of HHF (HR: 0.66, 95%CI 0.58–0.75; p < 0.001), ACD (HR: 0.52, 95%CI 0.45–0.60; p < 0.001), the composite of HHF or ACD (HR: 0.60, 95%CI 0.53–0.68; p < 0.001), MI (HR: 0.85, 95%CI 0.78–0.92; p < 0.001), and stroke (HR: 0.78, 95%CI 0.72–0.85; p < 0.001); regardless of patient characteristics, including established cardiovascular disease, or geographic region. Conclusions: This CVD-REAL study extends the findings from the SGLT-2i clinical trials to the broader setting of an ethnically and geographically diverse population, and across multiple subgroups.
AB - Background: Randomized, controlled cardiovascular outcome trials may not be fully representative of the management of patients with type 2 diabetes across different geographic regions. We conducted analyses of data from the multinational CVD-REAL consortium to determine the association between initiation of sodium–glucose cotransporter-2 inhibitors (SGLT-2i) and cardiovascular outcomes, including subgroup analyses based on patient characteristics. Methods: De-identified health records from 13 countries across three continents were used to identify patients newly-initiated on SGLT-2i or other glucose-lowering drugs (oGLDs). Propensity scores for SGLT-2i initiation were developed in each country, with 1:1 matching for oGLD initiation. In the matched groups hazard ratios (HRs) for hospitalization for heart failure (HHF), all-cause death (ACD), the composite of HHF or ACD, myocardial infarction (MI) and stroke were estimated by country, and pooled using a weighted meta-analysis. Multiple subgroup analyses were conducted across patient demographic and clinical characteristics to examine any heterogeneity in treatment effects. Results: Following matching, 440,599 new users of SGLT-2i and oGLDs were included in each group. Mean follow-up time was 396 days for SGLT-2i initiation and 406 days for oGLDs initiation. SGLT-2i initiation was associated with a lower risk of HHF (HR: 0.66, 95%CI 0.58–0.75; p < 0.001), ACD (HR: 0.52, 95%CI 0.45–0.60; p < 0.001), the composite of HHF or ACD (HR: 0.60, 95%CI 0.53–0.68; p < 0.001), MI (HR: 0.85, 95%CI 0.78–0.92; p < 0.001), and stroke (HR: 0.78, 95%CI 0.72–0.85; p < 0.001); regardless of patient characteristics, including established cardiovascular disease, or geographic region. Conclusions: This CVD-REAL study extends the findings from the SGLT-2i clinical trials to the broader setting of an ethnically and geographically diverse population, and across multiple subgroups.
KW - Cardiovascular outcomes
KW - Heart failure
KW - Sodium–glucose cotransporter-2 inhibitors
KW - Type 2 diabetes
UR - http://www.scopus.com/inward/record.url?scp=85112263464&partnerID=8YFLogxK
U2 - 10.1186/s12933-021-01345-z
DO - 10.1186/s12933-021-01345-z
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 34332558
AN - SCOPUS:85112263464
SN - 1475-2840
VL - 20
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
IS - 1
M1 - 159
ER -