Sodium-Glucose Cotransporter-2 Inhibitors and Primary Prevention of Atherosclerotic Cardiovascular Disease: A Meta-Analysis of Randomized Trials and Systematic Review

被引:23
作者
Rahman, Hammad [1 ,7 ]
Khan, Safi U. U. [2 ]
Lone, Ahmad N. N. [1 ]
Ghosh, Priyanka [1 ]
Kunduru, Mahathi [3 ]
Sharma, Saurabh [4 ]
Sattur, Sudhakar [4 ]
Kaluski, Edo [4 ,5 ,6 ]
机构
[1] Guthrie Robert Packer Hosp, Div Cardiol, Sayre, PA USA
[2] Methodist Hosp, Div Cardiol, Houston, TX USA
[3] Guthrie Robert Packer Hosp, Dept Med, Sayre, PA USA
[4] Robert Packer Hosp, Guthrie Hlth Syst, Div Cardiol, Sayre, PA USA
[5] Rutgers New Jersey Med Sch, Div Cardiol, Newark, NJ USA
[6] Geisinger Commonwealth Med Coll, Div Cardiol, Scranton, PA USA
[7] Guthrie Robert Packer Hosp, 1 Guthrie Sq, Sayre, PA 18840 USA
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2023年 / 12卷 / 16期
关键词
atherosclerotic major adverse cardiovascular events; primary prevention; sodium-glucose cotransporter-2 inhibitors; CHRONIC KIDNEY-DISEASE;
D O I
10.1161/JAHA.123.030578
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundSodium-glucose cotransporter-2 (SGLT2) inhibitors reduce atherosclerotic cardiovascular disease (ASCVD) events in patients with prior ASCVD and type 2 diabetes; however, this benefit is uncertain in patients without established ASCVD. Methods and ResultsLarge-scale cardiovascular outcome randomized controlled trials or their prespecified subgroup analyses were selected, evaluating SGLT2 inhibitors versus placebo for primary prevention of ASCVD (inception, March 2023). The primary outcome was atherosclerotic major adverse cardiovascular events (MACEs), which was a composite of cardiovascular mortality, myocardial infarction, and stroke. The secondary outcomes were individual components of MACEs and all-cause mortality. The outcomes were reported as random-effect relative risk (RR) with a 95% CI. This analysis, comprising 23 987 patients enrolled in 5 randomized controlled trials with a mean follow-up duration of & AP;135 weeks, found no significant reduction in atherosclerotic MACEs with SGLT2 inhibitors in comparison to placebo (RR, 0.85 [95% CI, 0.71-1.01]; P=0.07; I-2=44). There were no significant differences in cardiovascular mortality (RR, 0.93 [95% CI, 0.77-1.14]; P=0.50; I-2=0), myocardial infarction (RR, 0.88 [95% CI, 0.69-1.11]; P=0.28; I-2=23), and stroke (RR, 0.84 [95% CI, 0.62-1.16]; P=0.29; I-2=46). SGLT2 inhibitors significantly improved all-cause mortality (RR, 0.85 [95% CI, 0.72-1.0]; P=0.04; I-2=23). On subgroup analyses, the use of SGLT2 inhibitors led to significant reductions in MACEs (RR, 0.74 [95% CI, 0.61-0.89]; P=0.001), myocardial infarction (RR, 0.67 [95% CI, 0.47-0.97]; P=0.03), and stroke (RR, 0.61 [95% CI, 0.41-0.91]; P=0.01) primarily in patients with chronic kidney disease along with type 2 diabetes, whereas these benefits were not observed in patients with type 2 diabetes without chronic kidney disease. ConclusionsSGLT2 inhibitors significantly reduced atherosclerotic MACEs in subjects having both chronic kidney disease and type 2 diabetes without established ASCVD.
引用
收藏
页数:18
相关论文
共 29 条
[1]  
Ahajournals, AHAASA J
[2]   Sodium-Glucose Cotransporter 2 Inhibition for the Prevention of Cardiovascular Events in Patients With Type 2 Diabetes Mellitus: A Systematic Review and Meta-Analysis [J].
Arnott, Clare ;
Li, Qiang ;
Kang, Amy ;
Neuen, Brendon L. ;
Bompoint, Severine ;
Lam, Carolyn S. P. ;
Rodgers, Anthony ;
Mahaffey, Kenneth W. ;
Cannon, Christopher P. ;
Perkovic, Vlado ;
Jardine, Meg J. ;
Neal, Bruce .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2020, 9 (03)
[3]   Sotagliflozin in Patients with Diabetes and Chronic Kidney Disease [J].
Bhatt, Deepak L. ;
Szarek, Michael ;
Pitt, Bertram ;
Cannon, Christopher P. ;
Leiter, Lawrence A. ;
McGuire, Darren K. ;
Lewis, Julia B. ;
Riddle, Matthew C. ;
Inzucchi, Silvio E. ;
Kosiborod, Mikhail N. ;
Cherney, David Z. I. ;
Dwyer, Jamie P. ;
Scirica, Benjamin M. ;
Bailey, Clifford J. ;
Diaz, Rafael ;
Ray, Kausik K. ;
Udell, Jacob A. ;
Lopes, Renato D. ;
Lapuerta, Pablo ;
Steg, P. Gabriel .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 384 (02) :129-139
[4]  
Bhatt DL., 2022, ACC
[5]   Sodium-Glucose Co-Transporter 2 (SGLT2) Inhibitor Dapagliflozin Stabilizes Diabetes-Induced Atherosclerotic Plaque Instability [J].
Chen, Yung-Chih ;
Jandeleit-Dahm, Karin ;
Peter, Karlheinz .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2022, 11 (01)
[6]   Bias in meta-analysis detected by a simple, graphical test [J].
Egger, M ;
Smith, GD ;
Schneider, M ;
Minder, C .
BMJ-BRITISH MEDICAL JOURNAL, 1997, 315 (7109) :629-634
[7]   SGLT2 Inhibitor-associated Diabetic Ketoacidosis: Clinical Review and Recommendations for Prevention and Diagnosis [J].
Goldenberg, Ronald M. ;
Berard, Lori D. ;
Cheng, Alice Y. Y. ;
Gilbert, Jeremy D. ;
Verma, Subodh ;
Woo, Vincent C. ;
Yale, Jean-Francois .
CLINICAL THERAPEUTICS, 2016, 38 (12) :2654-2664
[8]   Dapagliflozin in Patients with Chronic Kidney Disease [J].
Heerspink, Hiddo J. L. ;
Stefansson, Bergur V. ;
Correa-Rotter, Ricardo ;
Chertow, Glenn M. ;
Greene, Tom ;
Hou, Fan-Fan ;
Mann, Johannes F. E. ;
McMurray, John J. V. ;
Lindberg, Magnus ;
Rossing, Peter ;
Sjostrom, C. David ;
Toto, Roberto D. ;
Langkilde, Anna-Maria ;
Wheeler, David C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (15) :1436-1446
[9]  
Heidenreich PA, 2022, CIRCULATION, V145, pE895, DOI [10.1016/j.jacc.2021.12.011, 10.1161/CIR.0000000000001063]
[10]   Empagliflozin in Patients with Chronic Kidney Disease [J].
Herrington, William G. ;
Staplin, Natalie ;
Wanner, Christoph ;
Green, Jennifer B. ;
Hauske, Sibylle J. ;
Emberson, Jonathan R. ;
Preiss, David ;
Judge, Parminder ;
Mayne, Kaitlin J. ;
Ng, Sarah Y. A. ;
Sammons, Emily ;
Zhu, Doreen ;
Hill, Michael ;
Stevens, Will ;
Wallendszus, Karl ;
Brenner, Susanne ;
Cheung, Alfred K. ;
Liu, Zhi-Hong ;
Li, Jing ;
Hooi, Lai Seong ;
Liu, Wen ;
Kadowaki, Takashi ;
Nangaku, Masaomi ;
Levin, Adeera ;
Cherney, David ;
Maggioni, Aldo P. ;
Pontremoli, Roberto ;
Deo, Rajat ;
Goto, Shinya ;
Rossello, Xavier ;
Tuttle, Katherine R. ;
Steubl, Dominik ;
Petrini, Michaela ;
Massey, Dan ;
Eilbracht, Jens ;
Brueckmann, Martina ;
Landray, Martin J. ;
Baigent, Colin ;
Haynes, Richard .
NEW ENGLAND JOURNAL OF MEDICINE, 2023, 388 (02) :117-127