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β-Blockers and Asthma: Surprising findings from the FAERS database
Mario Cazzola1, Josuel Ora2, Luigino Calzetta3
1Unit of Respiratory Medicine, Department of Experimental Medicine, University of Rome 'Tor Vergata', Rome, Italy.
Selective β1-blockers show a higher risk of asthma-like events compared to non-selective beta-blockers. This study highlights the need for careful beta-blocker selection in patients with asthma or predisposition to respiratory conditions.
Area of Science:
- Pharmacology and Therapeutics
- Cardiovascular Disease Management
- Respiratory Medicine
Background:
- Beta-blockers are crucial for managing cardiovascular diseases but can cause respiratory issues, especially non-selective agents.
- The safety of beta-blockers in patients with asthma remains a significant clinical concern and subject to ongoing debate.
Purpose of the Study:
- To investigate the association between different classes of beta-blockers and the risk of asthma or asthma-like adverse events.
- To evaluate beta-blocker safety profiles in asthmatic patients using real-world data.
Main Methods:
- Utilized the Food and Drug Administration's Adverse Event Reporting System (FAERS) database.
- Employed disproportionality analysis, calculating the reporting odds ratio (ROR) to assess asthma risk signals.
- Classified beta-blockers using both the European Society of Cardiology and Vashistha and Kumar systems.
Main Results:
- A total of 4104 asthma-related adverse events were identified among 251,145 reported beta-blocker events.
- Selective β1-blockers exhibited a higher asthma risk signal (ROR: 1.15) than non-selective beta-blockers (ROR: 0.90).
- Dual α- and β-blockers demonstrated the lowest asthma risk (ROR: 0.51), with variations observed across different classifications and properties (e.g., lipophilicity).
Conclusions:
- The study identified significant variability in asthma-related risks among different beta-blocker classes, necessitating cautious selection in patients with asthma.
- Specific beta-blockers like esmolol, metoprolol, nebivolol, and nadolol may be preferable, while betaxolol, bisoprolol, timolol, and propranolol warrant avoidance.
- Findings underscore the importance of risk stratification for beta-blocker use in vulnerable patient populations, despite FAERS data limitations.
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