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Selectivity of beta-blockers, cardiovascular and all-cause mortality in people with hypoglycaemia: An observational
F Zaccardi1, L L Nystrup Husemoen2, B L Thorsted2
1Diabetes Research Centre, University of Leicester, Gwendolen Rd, Leicester, LE5 4PW, UK.
Insights
Beta-blocker selectivity impacts mortality risk in diabetic patients. Beta1-selective beta-blockers may reduce death risk in patients experiencing hypoglycaemia, warranting further investigation.
Area of Science:
- Cardiology
- Diabetology
- Pharmacology
Background:
- The relationship between beta-blocker use, selectivity, and outcomes in diabetic patients with and without hypoglycemia remains unclear.
- Hypoglycemia is a common complication in insulin-treated diabetes, potentially influenced by cardiovascular medications.
Purpose of the Study:
- To investigate the association of beta-blocker therapy and selectivity with mortality and cardiovascular events.
- To assess the interaction between beta-blocker use, selectivity, and hypoglycemia in insulin-treated diabetic patients.
Main Methods:
- Utilized the UK CPRD database to identify insulin-treated diabetic patients.
- Captured data on all-cause deaths, cardiovascular events, and hypoglycemic episodes.
- Analyzed the association between beta-blocker therapy (non-selective vs. beta1-selective) and outcomes, considering hypoglycemia as an interaction factor.
Main Results:
- No significant association between any beta-blocker use and mortality risk, irrespective of hypoglycemia.
- Non-selective beta-blockers were linked to a higher mortality risk in patients without hypoglycemia (HR 1.59 [1.22-2.08] post-imputation).
- Beta1-selective beta-blockers showed a potential reduced risk of death in patients with hypoglycemia (HR 0.76 [0.61-0.94] post-imputation).
Conclusions:
- Beta1-selective beta-blockers may offer a survival benefit in diabetic patients experiencing hypoglycemic episodes.
- These findings are exploratory and require validation due to potential confounding by indication.
Background And Aims:
The association of beta-blockers and their selectivity with mortality and cardiovascular events in patients with and without hypoglycaemia is unknown.
Methods And Results:
Insulin-treated patients with diabetes were identified within the UK CPRD database. All-cause deaths, cardiovascular events, and hypoglycaemic episodes were captured to assess the interaction between beta-blocker therapy and selectivity with hypoglycaemia. 13,682 patients, of which 2036 (14.9%) with at least one hypoglycaemic episode, were included; 3148 deaths and 1235 cardiovascular events were recorded during a median of 2.3 and 4.7 years in patients with and without incident hypoglycaemia, respectively. Treatment with any beta-blocker was not associated with risk of death in both patients with and without hypoglycaemia, without significant interaction. Compared to no therapy, non-selective beta-blockers were associated with higher risk of death in patients without hypoglycaemia (hazard ratio (HR) 2.93 [1.26-6.83] in the fully adjusted model) but not in those with hypoglycaemia; interactions was not significant. For beta1-selective beta-blockers, there was no association with mortality in both patients with and without hypoglycaemia, without significant interaction. After missing data imputation, results were consistent for non-selective beta-blockers (HR in patients without hypoglycaemia 1.59 [1.22-2.08]) while indicated a reduced risk of death for beta1-selective beta-blockers in patients with hypoglycaemia (HR 0.76 [0.61-0.94]). Due to few cardiovascular events, complete-case analysis compared only any vs no beta-blocker therapy and indicated no associations with therapy or interaction by hypoglycaemia.
Conclusion:
In patients with hypoglycaemic episodes, treatment with beta1-selective beta-blockers may potentially reduce the risk of death. These explorative findings and the potential role of confounding by indication need to be evaluated in other studies.
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