2026
GLP-1 receptor agonists for secondary prevention after myocardial infarction and stroke in type 2 diabetes: nationwide real-world evidence
ŠEDOVÁ, Petra; Michal VRABLIK; Petr KALA; Petr OSTADAL; Ales TICHOPAD et al.Základní údaje
Originální název
GLP-1 receptor agonists for secondary prevention after myocardial infarction and stroke in type 2 diabetes: nationwide real-world evidence
Autoři
ŠEDOVÁ, Petra; Michal VRABLIK; Petr KALA; Petr OSTADAL; Ales TICHOPAD; Ales TOMEK; Robert MIKULÍK; Gleb DONIN; Simona LITTNEROVÁ; Julia Anna KENT; Jiří JARKOVSKÝ ORCID; Virend K SOMERS a Robert D BROWN JR
Vydání
EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY, OXFORD, OXFORD UNIV PRESS, 2026, 2047-4873
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30201 Cardiac and Cardiovascular systems
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 7.500 v roce 2024
Označené pro přenos do RIV
Ne
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Glucagon-like peptide-1 receptor agonists (GLP-1 RA); Type 2 diabetes; Myocardial infarction; Stroke; Major adverse cardiovascular events (MACE); Health disparities
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 7. 4. 2026 14:40, Mgr. Tereza Miškechová
Anotace
V originále
Aims Glucagon-like peptide-1 receptor agonists (GLP-1RA) reduce cardiovascular risk in patients with Type 2 diabetes (T2D) and established atherosclerotic cardiovascular disease and are recommended in guidelines. We evaluated the real-world effectiveness of GLP-1RA therapy on cardiovascular outcomes in patients with T2D after myocardial infarction (MI) or ischaemic stroke and examined trends and disparities. Methods and results Using nationwide Czech registry data (2015-24), we identified patients with incident nonfatal MI or ischaemic stroke and confirmed T2D. GLP-1RA users-initiating therapy within 12 months post-event-were propensity score matched to non-users. The primary outcome was major adverse cardiovascular events (MACE: nonfatal MI, nonfatal stroke, cardiovascular death); secondary outcomes included individual components and all-cause mortality. GLP-1RA therapy was initiated in only similar to 2% of MI and stroke survivors with T2D. Among 126 845 MI survivors, 28 206 had T2D; the matched cohort comprised 2271 patients (401 GLP-1RA; median follow-up 35 months). GLP-1RA use was associated with lower risk of MACE (HR 0.7; 95% CI, 0.52-0.93), all-cause (HR 0.61; 95% CI, 0.47-0.80), and cardiovascular death (HR 0.54; 95% CI, 0.36-0.80). Among 177 115 stroke survivors, 73 750 had T2D; the matched cohort comprised 2235 patients (385 GLP-1RA; median follow-up 27 months). GLP-1RA use was associated with lower risk of MACE (HR 0.71; 95% CI, 0.54-0.94), all-cause (HR 0.59; 95% CI, 0.46-0.76), and cardiovascular death (HR 0.55; 95% CI, 0.37-0.81). Conclusion GLP-1RA therapy after MI or stroke in T2D was associated with substantially lower risks of MACE, cardiovascular, and all-cause death in real-world practice. Utilization remained low, particularly among women and older adults, underscoring the need for broader and more equitable implementation in secondary prevention.
Návaznosti
| NW24-09-00215, projekt VaV |
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