Type 2 & other diabetes

Eplerenone, diabetes, and chronic kidney disease in patients hospitalized for acute heart failure: findings from the EARLIER trial

Cardiovasc DiabetolPublished Secondary analysis of the EARLIER randomised trial

Authors' conclusion

In patients with acute HF, the combination of diabetes and CKD was associated with an increased risk of cardiovascular events. However, the efficacy and safety of eplerenone were not influenced by diabetes and CKD status.

Study context

Population
Patients hospitalized for acute heart failure (HF) in the EARLIER trial, randomized to eplerenone or placebo for 6 months; mean age 67 ± 13 years, 73% male, 39% diabetes, 58% chronic kidney disease (CKD)
Participants
300 patients
Comparison
Diabetes and CKD vs neither disease; eplerenone vs placebo across diabetes/CKD categories
Primary endpoint
Associations between diabetes/CKD categories and cardiovascular outcomes; effects of eplerenone on HF-related outcomes (CV death, HF hospitalization, worsening HF or out-of-hospital diuretic intensification) and adverse events across diabetes/CKD status
Methodological detailsplacebo-controlled, subgroup analysis by diabetes/CKD status
  • Placebo-controlled
  • Subgroup analysis by diabetes/CKD status

Primary result

As reported in the abstract

CV death and/or hospitalization
Diabetes and CKD vs Neither diseaseEstimate (95% CI)P value
P-for-interaction = 0.049
HR 2.57(1.29–5.12)
P = 0.007
Adjusted for covariates (i.e., natriuretic peptide)
adjusted HR 2.33(1.12–4.84)
P = 0.02
Effects of eplerenone on HF-related outcomes consistent regardless of diabetes/CKD categories
all-P-for interaction > 0.05

Safety

Adverse events with eplerenone across diabetes/CKD categories

Effects of eplerenone on adverse events consistent regardless of diabetes/CKD categories
all-P-for interaction > 0.05

Original publication

Eplerenone, diabetes, and chronic kidney disease in patients hospitalized for acute heart failure: findings from the EARLIER trial. Cardiovasc Diabetol. Published 22 March 2025. doi:10.1186/s12933-025-02659-y

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.