Pregled bibliografske jedinice broj: 736879
Alogliptin after Acute Coronary Syndrome in Patients with Type 2 Diabetes
Alogliptin after Acute Coronary Syndrome in Patients with Type 2 Diabetes // The New England journal of medicine, 369 (2013), 1327-1335 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 736879 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Alogliptin after Acute Coronary Syndrome in Patients with Type 2 Diabetes
Autori
White, WB ; Cannon, CP ; Heller, SR ; Nissen, SE ; Bergenstal, RM ; Bakris, GL ; Perez, AT ; Fleck, PR ; Mehta, CR ; Kupfer, S ; Wilson, C ; Cushman, WC Zannad, F ; ... ; Knežević, Aleksandar ; ...
Izvornik
The New England journal of medicine (0028-4793) 369
(2013);
1327-1335
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Sažetak
To assess potentially elevated cardiovascular risk related to new antihyperglycemic drugs in patients with type 2 diabetes, regulatory agencies require a comprehensive evaluation of the cardiovascular safety profile of new antidiabetic therapies. We assessed cardiovascular outcomes with alogliptin, a new inhibitor of dipeptidyl peptidase 4 (DPP-4), as compared with placebo in patients with type 2 diabetes who had had a recent acute coronary syndrome. We randomly assigned patients with type 2 diabetes and either an acute myocar - dial infarction or unstable angina requiring hospitalization within the previous 15 to 90 days to receive alogliptin or placebo in addition to existing antihyperglycemic and cardiovascular drug therapy. The study design was a double-blind, noninferiority trial with a prespecified noninferiority margin of 1.3 for the hazard ratio for the primary end point of a composite of death from cardiovascular causes, nonfatal myo - cardial infarction, or nonfatal stroke. A total of 5380 patients underwent randomization and were followed for up to 40 months (median, 18 months). A primary end-point event occurred in 305 patients assigned to alogliptin (11.3%) and in 316 patients assigned to placebo (11.8%) (haz - ard ratio, 0.96 ; upper boundary of the one-sided repeated confidence interval, 1.16 ; P<0.001 for noninferiority). Glycated hemoglobin levels were significantly lower with alogliptin than with placebo (mean difference, −0.36 percentage points ; P<0.001). Incidences of hypoglycemia, cancer, pancreatitis, and initiation of dialysis were similar with alogliptin and placebo. Among patients with type 2 diabetes who had had a recent acute coronary syn - drome, the rates of major adverse cardiovascular events were not increased with the DPP-4 inhibitor alogliptin as compared with placebo.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
Napomena
EXAMINE Investigators.
POVEZANOST RADA
Ustanove:
Sveučilište u Zadru,
Opća bolnica Zadar
Profili:
Aleksandar Knežević
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE