Your browser doesn't support javascript.
loading
Cardiovascular, renal, and lower limb outcomes in patients with type 2 diabetes after percutaneous coronary intervention and treated with sodium-glucose cotransporter 2 inhibitors vs. dipeptidyl peptidase-4 inhibitors.
Lee, Hsin-Fu; Chan, Yi-Hsin; Chuang, Chi; Li, Pei-Ru; Yeh, Yung-Hsin; Hsiao, Fu-Chih; Peng, Jian-Rong; See, Lai-Chu.
Affiliation
  • Lee HF; Division of Cardiology, Department of Internal Medicine, New Taipei City Municipal Tucheng Hospital, New Taipei City 23652, Taiwan.
  • Chan YH; The Cardiovascular Department, Chang Gung Memorial Hospital, Linkou, Taoyuan City 33305, Taiwan.
  • Chuang C; College of Medicine, Chang Gung University, Taoyuan City 33302, Taiwan.
  • Li PR; Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan City 33302, Taiwan.
  • Yeh YH; The Cardiovascular Department, Chang Gung Memorial Hospital, Linkou, Taoyuan City 33305, Taiwan.
  • Hsiao FC; College of Medicine, Chang Gung University, Taoyuan City 33302, Taiwan.
  • Peng JR; Microscopy Core Laboratory, Chang Gung Memorial Hospital, Linkou, Taoyuan City 33305, Taiwan.
  • See LC; Division of Cardiology, Department of Internal Medicine, New Taipei City Municipal Tucheng Hospital, New Taipei City 23652, Taiwan.
Eur Heart J Cardiovasc Pharmacother ; 9(4): 301-310, 2023 06 02.
Article in En | MEDLINE | ID: mdl-36639127
ABSTRACT

AIMS:

Patients with type 2 diabetes (T2D) who undergo percutaneous coronary intervention (PCI) are at higher risk of adverse cardiovascular and renal events than non-diabetic patients. However, limited evidence is available regarding the cardiovascular, renal, and limb outcomes of patients with T2D after PCI and who were treated with sodium-glucose cotransporter-2 inhibitors (SGLT2i). We compare the specified outcomes in patients with T2D after PCI who were treated with SGLT2i vs. dipeptidyl peptidase-4 inhibitors (DPP4i). METHODS AND

RESULTS:

In this nationwide retrospective cohort study, we identified 4248 and 37 037 consecutive patients with T2D who underwent PCI with SGLT2i and DPP4i, respectively, for 1 May 2016-31 December 2019. We used propensity score matching (PSM) to balance the covariates between study groups. After PSM, SGLT2i, and DPP4i were associated with comparable risks of ischaemic stroke, acute myocardial infarction, and lower limb amputation. However, SGLT2i was associated with significantly lower risks of heart failure hospitalization [HFH; 1.35% per year vs. 2.28% per year; hazard ratio (HR) 0.60; P = 0.0001], coronary revascularization (2.33% per year vs. 3.36% per year; HR 0.69; P = 0.0003), composite renal outcomes (0.10% per year vs. 1.05% per year; HR 0.17; P < 0.0001), and all-cause mortality (2.27% per year vs. 3.80% per year, HR 0.60; P < 0.0001) than were DPP4i.

CONCLUSION:

Our data indicated that SGLT2i, compared with DPP4i, were associated with lower risks of HFH, coronary revascularization, composite renal outcomes, and all-cause mortality for patients with T2D after PCI. Further randomized or prospective studies can investigate the effects of SGLT2i in patients with T2D after PCI.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Ischemia / Stroke / Diabetes Mellitus, Type 2 / Dipeptidyl-Peptidase IV Inhibitors / Percutaneous Coronary Intervention / Sodium-Glucose Transporter 2 Inhibitors Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Eur Heart J Cardiovasc Pharmacother Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Ischemia / Stroke / Diabetes Mellitus, Type 2 / Dipeptidyl-Peptidase IV Inhibitors / Percutaneous Coronary Intervention / Sodium-Glucose Transporter 2 Inhibitors Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Eur Heart J Cardiovasc Pharmacother Year: 2023 Document type: Article