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Abstract
Previous studies have explored the effects of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) in reducing cardiovascular events in type 2 diabetes. Here we show that GLP-1 RAs are associated with lower risks of mortality, major cardiovascular events (MACEs), and major adverse kidney events (MAKEs) in type 2 diabetes patients with acute kidney disease (AKD). Utilizing global data from the TriNetX database (2002/09/01-2022/12/01) and propensity score matching, we compare 7511 GLP-1 RAs users to non-users among 165,860 AKD patients. The most common causes of AKI are sepsis (55.2%) and cardiorenal syndrome (34.2%). After a median follow-up of 2.3 years, GLP-1 RAs users exhibit reduced risks of mortality (adjusted hazard ratio [aHR]: 0.57), MACEs (aHR: 0.88), and MAKEs (aHR: 0.73). External validation in a multicenter dataset of 1245 type 2 diabetes patients with AKD supports the favorable outcomes. These results emphasize the potential of GLP-1 RAs in individualized treatment for this population.
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have been studied for their cardiovascular benefits in type 2 diabetes. Here, the authors show that GLP-1 RAs are associated with reduced mortality and improved cardio-renal outcomes in type 2 diabetes patients with acute kidney disease.
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1 College of Medicine, National Taiwan University, Graduate Institute of Clinical Medicine, Taipei, Taiwan (GRID:grid.19188.39) (ISNI:0000 0004 0546 0241); Chang Gung University College of Medicine, Taoyuan, Taiwan (GRID:grid.413801.f) (ISNI:0000 0001 0711 0593); Keelung Chang Gung Memorial Hospital, Division of Nephrology, Department of Internal Medicine, Keelung, Taiwan (GRID:grid.454209.e) (ISNI:0000 0004 0639 2551); Keelung Chang Gung Memorial Hospital, Community Medicine Research Center, Keelung, Taiwan (GRID:grid.454209.e) (ISNI:0000 0004 0639 2551); Linkou Chang Gung Memorial Hospital, Kidney Research Center and Department of Nephrology, Taoyuan, Taiwan (GRID:grid.454211.7) (ISNI:0000 0004 1756 999X)
2 Chi Mei Medical Center, Division of Nephrology, Department of Internal Medicine, Tainan, Taiwan (GRID:grid.413876.f) (ISNI:0000 0004 0572 9255); Chia Nan University of Pharmacy and Science, Department of Health and Nutrition, Tainan, Taiwan (GRID:grid.411315.3) (ISNI:0000 0004 0634 2255)
3 College of Medicine, Chang Gung University, Graduate Institute of Clinical Medical Sciences, Taoyuan, Taiwan (GRID:grid.145695.a) (ISNI:0000 0004 1798 0922); Center for Traditional Chinese Medicine, Chang Gung Memorial Hospital, Division of Chinese Internal Medicine, Taoyuan, Taiwan (GRID:grid.413801.f) (ISNI:0000 0001 0711 0593); College of Medicine, Chang Gung University, School of Traditional Chinese Medicine, Taoyuan, Taiwan (GRID:grid.145695.a) (ISNI:0000 0004 1798 0922)
4 National Taiwan University Hospital, Division of Nephrology, Primary Aldosteronism Center of Internal Medicine, Taipei, Taiwan (GRID:grid.412094.a) (ISNI:0000 0004 0572 7815)
5 Keelung Chang Gung Memorial Hospital, Division of Nephrology, Department of Internal Medicine, Keelung, Taiwan (GRID:grid.454209.e) (ISNI:0000 0004 0639 2551); Linkou Chang Gung Memorial Hospital, Kidney Research Center and Department of Nephrology, Taoyuan, Taiwan (GRID:grid.454211.7) (ISNI:0000 0004 1756 999X)
6 National Taiwan University Hospital, Division of Nephrology, Primary Aldosteronism Center of Internal Medicine, Taipei, Taiwan (GRID:grid.412094.a) (ISNI:0000 0004 0572 7815); and CAKS (Taiwan Consortium for Acute Kidney Injury and Renal Diseases), NSARF (National Taiwan University Hospital Study Group of ARF), Taipei, Taiwan (GRID:grid.412094.a) (ISNI:0000 0004 0572 7815)