TY - JOUR
T1 - Comparative cardiovascular and renal outcomes of Liraglutide versus Dulaglutide in Asian type 2 diabetes patients
AU - Dai, Jhih Wei
AU - Lin, Yuan
AU - Li, Xiu Wei
AU - Tseng, Chin Ju
AU - Tsai, Ming Lung
AU - Yang, Ning I.
AU - Hung, Ming Jui
AU - Chen, Tien Hsing
N1 - © 2024. The Author(s).
PY - 2024/12
Y1 - 2024/12
N2 - Given the limited head-to-head comparison of cardiovascular and renal outcomes between liraglutide and dulaglutide, our study aimed to investigate the clinical outcomes between dulaglutide and liraglutide in a real-world setting. In this new-user design, comparative and retrospective cohort study, patients with type 2 diabetes mellitus with prescription for GLP-1RAs from January 1, 2016 to December 31, 2022 (n = 8,278) were included. Primary outcome was composite cardiovascular outcomes which was composed of cardiovascular death, non-fatal myocardial infarction, and non-fatal ischemic stroke. The composite renal outcome was also interested, including new macroalbuminuria, doubling of serum creatinine, worsening of estimated glomerular filtration rate (eGFR), and progression to dialysis. A total of 3,210 subjects receiving liraglutide and 5,068 subjects receiving dulaglutide were identified. In the adjusted cohort by applying inverse probability of treatment weighting, the incidence of composite cardiovascular outcomes was 18.4 and 18.7 events per 1000 person-years in the liraglutide and dulaglutide groups, respectively. The risk of cardiovascular outcomes did not significantly differ between groups (hazard ratio [HR] 0.99, 95% confidence interval [CI] 0.85–1.15). Moreover, the risk of composite renal outcomes was also comparable between groups (subdistribution HR 1.07, 95% CI 0.995–1.16). Liraglutide and dulaglutide demonstrated comparable cardiovascular and renal outcomes in a real-world setting.
AB - Given the limited head-to-head comparison of cardiovascular and renal outcomes between liraglutide and dulaglutide, our study aimed to investigate the clinical outcomes between dulaglutide and liraglutide in a real-world setting. In this new-user design, comparative and retrospective cohort study, patients with type 2 diabetes mellitus with prescription for GLP-1RAs from January 1, 2016 to December 31, 2022 (n = 8,278) were included. Primary outcome was composite cardiovascular outcomes which was composed of cardiovascular death, non-fatal myocardial infarction, and non-fatal ischemic stroke. The composite renal outcome was also interested, including new macroalbuminuria, doubling of serum creatinine, worsening of estimated glomerular filtration rate (eGFR), and progression to dialysis. A total of 3,210 subjects receiving liraglutide and 5,068 subjects receiving dulaglutide were identified. In the adjusted cohort by applying inverse probability of treatment weighting, the incidence of composite cardiovascular outcomes was 18.4 and 18.7 events per 1000 person-years in the liraglutide and dulaglutide groups, respectively. The risk of cardiovascular outcomes did not significantly differ between groups (hazard ratio [HR] 0.99, 95% confidence interval [CI] 0.85–1.15). Moreover, the risk of composite renal outcomes was also comparable between groups (subdistribution HR 1.07, 95% CI 0.995–1.16). Liraglutide and dulaglutide demonstrated comparable cardiovascular and renal outcomes in a real-world setting.
KW - Cardiovascular outcomes
KW - Dulaglutide
KW - Liraglutide
KW - Renal outcomes
KW - Immunoglobulin Fc Fragments/therapeutic use
KW - Glomerular Filtration Rate
KW - Humans
KW - Middle Aged
KW - Male
KW - Treatment Outcome
KW - Glucagon-Like Peptides/analogs & derivatives
KW - Diabetes Mellitus, Type 2/drug therapy
KW - Recombinant Fusion Proteins/therapeutic use
KW - Female
KW - Hypoglycemic Agents/therapeutic use
KW - Aged
KW - Retrospective Studies
KW - Liraglutide/therapeutic use
KW - Cardiovascular Diseases/etiology
KW - Asian People
UR - http://www.scopus.com/inward/record.url?scp=85209480141&partnerID=8YFLogxK
U2 - 10.1038/s41598-024-79255-9
DO - 10.1038/s41598-024-79255-9
M3 - 文章
C2 - 39528690
AN - SCOPUS:85209480141
SN - 2045-2322
VL - 14
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 27491
ER -