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August 23, 2022European Journal of Heart Failure30 citations

Albiglutide in patients with type 2 diabetes and heart failure: a post‐hoc analysis from Harmony Outcomes

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JFJoão Pedro FerreiraASAbhinav SharmaFVFrancisco Vasques‐Nóvoa

Key Points

  • To determine whether baseline heart failure history alters the effect of the GLP-1 receptor agonist albiglutide on heart failure outcomes in patients with type 2 diabetes and cardiovascular disease.
  • Post-hoc analysis of the Harmony Outcomes randomized trial including 9,462 patients with type 2 diabetes and cardiovascular disease randomized to albiglutide or placebo over a median follow-up of 1.6 years.

Structured PICO

Does albiglutide reduce cardiovascular death or heart failure hospitalization in patients with type 2 diabetes and cardiovascular disease, and does this effect vary by history of heart failure?

P
Population
9,462 patients with type 2 diabetes and cardiovascular disease, including 1,922 (20%) with a history of heart failure
I
Intervention
Albiglutide
C
Comparator
Placebo
O
Outcome
Composite of cardiovascular death or heart failure hospitalizationcomposite

In patients with type 2 diabetes and cardiovascular disease, albiglutide did not reduce heart failure-related events in those with a history of heart failure, suggesting GLP-1 receptor agonists may lack efficacy for heart failure outcomes.

Abstract

AIM: Glucagon-like peptide-1 receptor agonists (GLP1-RA) improve cardiovascular outcomes in patients with type 2 diabetes (T2D). However, some studies suggest that their effects in patients with heart failure (HF) may be attenuated. We aimed to explore the effects of the GLP1-RA albiglutide on HF outcomes in patients with and without HF history enrolled in the Harmony Outcomes trial. METHODS AND RESULTS: Harmony Outcomes enrolled patients with T2D and cardiovascular disease randomized to either albiglutide or placebo over a median follow-up of 1.6 years. A total of 9462 patients were included, of whom 1922 (20%) had HF history. Patients with HF had more cardiovascular comorbidities, poorer renal function, and had a three to four-fold higher risk of HF events compared to patients without HF. Compared to placebo, the effect of albiglutide on the composite of cardiovascular death or HF hospitalization was more pronounced among patients without HF (hazard ratio HR 0.73, 95% confidence interval CI 0.56-0.95) than in patients with HF (HR 1.06, 95% CI 0.79-1.43) (interaction p = 0.062). A similar pattern was observed for HF hospitalizations (interaction p = 0.025). The effect of albiglutide on cardiovascular death, sudden death or 'pump failure' death, and all-cause mortality was also attenuated among patients with HF history, but without significant interaction (p > 0.1). The benefit of albiglutide to reduce atherosclerotic events was consistent regardless of HF history. CONCLUSIONS: In patients with T2D and cardiovascular disease, albiglutide appeared to have no effect in reducing HF-related events among patients with HF history. These findings, placed in the context of other trials, suggest that GLP1-RA may not improve HF outcomes in patients with HF.

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Cite This Study

Ferreira et al. (2022) studied this question.

synapsesocial.com/papers/6a704606febe604dd7090e94https://doi.org/10.1002/ejhf.2660
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Also Consider

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