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Updated: Jul 8, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Beta-blockers for coronary heart disease in chronic kidney disease
Michel Chonchol1, Michal Benderly, Uri Goldbourt
1Division of Renal Diseases and Hypertension, University of Colorado Health Sciences Center, Box C-281, Denver, CO 80262, USA. Michel.Chonchol@uchsc.edu
Insights
Beta-blockers offer cardioprotective benefits in coronary heart disease patients, irrespective of chronic kidney disease (CKD) status. This study found similar risk reduction for major adverse cardiac events in patients with or without CKD when treated with beta-blockers.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Limited data exist on the interaction between beta-blocker therapy and chronic kidney disease (CKD) regarding cardiovascular outcomes.
- Investigating this relationship is crucial for optimizing treatment strategies in patients with coronary heart disease (CHD) and varying degrees of renal function.
Purpose of the Study:
- To determine if the cardioprotective effects of beta-blockers are modified by the presence of chronic kidney disease (CKD) in patients with coronary heart disease (CHD).
Main Methods:
- A post hoc analysis of the Bezafibrate Infarction Prevention (BIP) study cohort was conducted.
- Chronic kidney disease (CKD) was defined as an estimated glomerular filtration rate (GFR) <60 mL/min/1.73 m(2) using the MDRD equation.
- Cox proportional hazard models, adjusted for propensity score, were used to assess the risk of acute myocardial infarction (AMI) or sudden cardiac death (SCD).
Main Results:
- The study included 3075 CHD patients, with 18.5% having CKD. Of these, 43.1% received beta-blockers.
- After a median follow-up of 6.2 years, the adjusted hazard ratio (HR) for AMI or SCD was 0.87 (90% CI 0.71-1.06) for beta-blocker users without CKD, and 1.35 (90% CI 1.05-1.73) for non-users with CKD.
- Patients with both beta-blocker use and CKD had an adjusted HR of 1.06 (90% CI 0.76-1.46) compared to those without beta-blockers and without CKD.
Conclusions:
- Beta-blocker use appears to be associated with a reduced risk of major adverse cardiac events in patients with coronary heart disease (CHD).
- This cardioprotective association was observed consistently, regardless of whether patients had chronic kidney disease (CKD) or not.
- The findings suggest that beta-blockers remain a valuable therapeutic option for CHD patients with impaired renal function.
Background:
Limited data exist on whether the cardioprotective benefit of beta-blockers is modified by the presence of chronic kidney disease (CKD).
Methods:
A post hoc analysis of the data from the Bezafibrate Infarction Prevention (BIP) study was performed. CKD was defined according to the Modification of Diet in Renal Disease (MDRD) equation as an estimated glomerular filtration rate (GFR) <60 mL/min/1.73 m(2). The Cox proportional hazard model, including adjustment for propensity score, was used to estimate the hazard ratios (HR) for the composite endpoint combining acute myocardial infarction (AMI) or sudden cardiac death (SCD).
Results:
In this cohort of 3075 coronary heart disease (CHD) patients, 568 (18.5%) had CKD and 1185 (38.5%) were treated with beta-blockers. A total of 245 (43.1%) CKD patients received beta-blockers at baseline. The mean (+/- SD) estimated GFR in the CKD and non-CKD subgroups was 55 (+/- 4) and 73 (+/- 9) mL/min/1.73 m(2), respectively. After a median follow-up of 6.2 years, the crude incidence rates of AMI or SCD/1000 person years (PY) were 25.6, 21.9, 34.6 and 27.5 for the beta-blockers-/CKD-, beta-blockers+/CKD-, beta-blockers-/CKD+ and beta-blockers+/CKD+ groups, respectively. Compared to patients with beta-blockers-/CKD-, the adjusted HR of AMI or SCD was 0.87 (90% CI 0.71-1.06) for the beta-blockers+/CKD-, 1.35 (90% CI 1.05-1.73) for the beta-blockers-/CKD+ and 1.06 (90% CI 0.76-1.46) for the beta-blockers+/CKD+.
Conclusions:
These analyses suggest that the use of beta-blockers is associated with a reduction in event risk in patients with CHD regardless of the presence or absence of CKD.
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