TY - JOUR
T1 - Use of Sodium-Glucose Cotransporter 2 Inhibitors and Glucagonlike Peptide-1 Receptor Agonists in Patients with Diabetes and Cardiovascular Disease in Community Practice
AU - Nanna, Michael G.
AU - Kolkailah, Ahmed A.
AU - Page, Courtney
AU - Peterson, Eric D.
AU - Navar, Ann Marie
N1 - Funding Information:
Funding/Support: This study was supported by Janssen Pharmaceuticals .
Funding Information:
Conflict of Interest Disclosures: Dr Nanna reported grants from National Institute on Aging and research support from the American College of Cardiology Foundation supported by the George F. and Ann Harris Bellows Foundation during the conduct of the study. Dr Kolkailah reported support by the National Heart, Lung, and Blood Institute. Dr Page reported grants from Janssen Scientific during the conduct of the study. Dr Peterson reported personal fees from Novo Nordisk and Bayer; grants from Janssen, Bristol Myers Squibb, Amgen, and Esperion; serves on scientific advisory boards for Novartis, Pfizer, Novo Nordisk, and Bayer; and is a consultant for Cerner Inc during the conduct of the study. Dr Navar reported grants from Janssen, Bristol Myers Squibb, Esperion, Amgen, and Janssen to their institution during the conduct of the study and personal fees from Janssen, AstraZeneca, Bayer, Novartis, Novo Nordisk, Bristol Myers Squibb, Boehringer Ingelheim, Eli Lilly and Company, New Amsterdam, Pfizer, and Cerner outside the submitted work.
Publisher Copyright:
© 2023 American Medical Association. All rights reserved.
PY - 2023/1/11
Y1 - 2023/1/11
N2 - Importance: Recent national guidelines recommend sodium-glucose cotransporter 2 inhibitors (SGLT2i) and glucagonlike peptide-1 receptor agonists (GLP-1 RA) in patients with type 2 diabetes (T2D) and atherosclerotic cardiovascular disease (ASCVD); yet, there are limited data on the use of these agents in contemporary community practice. Objective: To evaluate the use of SGLT2i and GLP-1 RA in adults with T2D and ASCVD across a diverse sample of health care systems in the US. Design, Setting, and Participants: This multicenter, retrospective cohort study used electronic health record data from 88 US health care systems participating in Cerner Real World Data between January 2018 to March 2021. Adults with ASCVD and T2D taking at least 1 glucose-lowering medication, had end-stage kidney disease, or had stage 5 chronic kidney disease were excluded. Main Outcomes and Measures: Treatment with SGLT2i or GLP-1 RA. Results: A total of 321304 patients were identified with T2D and ASCVD ASCVD (130 280 female [40.5%]; median [IQR] age, 70.9 [62.9-78.0] years) who were potentially eligible for SGLT2i and/or GLP-1 RA, including 37754 Black individuals (11.8%), 51522 Hispanic individuals (16.0%), and 256008 White individuals (11.8%). From January 2018 to March 2021, the use of SGLT2i increased from 5.8% (11285 of 194264) to 12.9% (11058 of 85956), GLP-1 RA increased from 6.9% (13402 of 194264) to 13.8% (11901 of 85956), and use of either agent increased from 11.4% (22069 of 194264) to 23.2% (19909 of 85956). Those taking an SGLT2i or GLP-1 RA were younger, less frequently hospitalized in the year prior, and more likely to be taking additional secondary prevention medications. Treated and nontreated populations were similar in terms of race, ethnicity, and outpatient health care utilization. Sulfonylureas and dipeptidyl peptidase 4 inhibitors remained more commonly used than SGLT2i or GLP-1 RA through 2021. Conclusions and Relevance: In this study, uptake of SGLT2i and GLP-1 RA in adults with T2D and ASCVD increased modestly after guideline recommendations, although less than a quarter of persons with ASCVD and T2D receiving medical therapy were taking either. Further efforts are necessary to maximize the potential population benefit of these therapies in this high-risk population.
AB - Importance: Recent national guidelines recommend sodium-glucose cotransporter 2 inhibitors (SGLT2i) and glucagonlike peptide-1 receptor agonists (GLP-1 RA) in patients with type 2 diabetes (T2D) and atherosclerotic cardiovascular disease (ASCVD); yet, there are limited data on the use of these agents in contemporary community practice. Objective: To evaluate the use of SGLT2i and GLP-1 RA in adults with T2D and ASCVD across a diverse sample of health care systems in the US. Design, Setting, and Participants: This multicenter, retrospective cohort study used electronic health record data from 88 US health care systems participating in Cerner Real World Data between January 2018 to March 2021. Adults with ASCVD and T2D taking at least 1 glucose-lowering medication, had end-stage kidney disease, or had stage 5 chronic kidney disease were excluded. Main Outcomes and Measures: Treatment with SGLT2i or GLP-1 RA. Results: A total of 321304 patients were identified with T2D and ASCVD ASCVD (130 280 female [40.5%]; median [IQR] age, 70.9 [62.9-78.0] years) who were potentially eligible for SGLT2i and/or GLP-1 RA, including 37754 Black individuals (11.8%), 51522 Hispanic individuals (16.0%), and 256008 White individuals (11.8%). From January 2018 to March 2021, the use of SGLT2i increased from 5.8% (11285 of 194264) to 12.9% (11058 of 85956), GLP-1 RA increased from 6.9% (13402 of 194264) to 13.8% (11901 of 85956), and use of either agent increased from 11.4% (22069 of 194264) to 23.2% (19909 of 85956). Those taking an SGLT2i or GLP-1 RA were younger, less frequently hospitalized in the year prior, and more likely to be taking additional secondary prevention medications. Treated and nontreated populations were similar in terms of race, ethnicity, and outpatient health care utilization. Sulfonylureas and dipeptidyl peptidase 4 inhibitors remained more commonly used than SGLT2i or GLP-1 RA through 2021. Conclusions and Relevance: In this study, uptake of SGLT2i and GLP-1 RA in adults with T2D and ASCVD increased modestly after guideline recommendations, although less than a quarter of persons with ASCVD and T2D receiving medical therapy were taking either. Further efforts are necessary to maximize the potential population benefit of these therapies in this high-risk population.
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U2 - 10.1001/jamacardio.2022.3839
DO - 10.1001/jamacardio.2022.3839
M3 - Article
C2 - 36322056
AN - SCOPUS:85146193302
SN - 2380-6583
VL - 8
SP - 89
EP - 95
JO - JAMA Cardiology
JF - JAMA Cardiology
IS - 1
ER -