Mitochondrial Disorder Aggravated by Metoprolol
Cheryl Samuels1, Mary Kay Koenig1, Mariana Hernandez1
1Department of Pediatrics, University of Texas Medical School at Houston, Houston, TX, USA.
Case Reports in Pediatrics
|November 15, 2016
Summary
Beta-blockers like metoprolol can worsen respiratory distress in children with mitochondrial disorders. Discontinuation of the drug improved symptoms, suggesting it aggravated underlying muscle weakness in this pediatric case.
Area of Science:
- Cardiology
- Neurology
- Pediatrics
Background:
- Beta-adrenergic blocking agents (beta-blockers) are widely used for cardiac arrhythmias and hypertension.
- Adverse effects include fatigue, cramping, dizziness, and dyspnea, which may be amplified in mitochondrial disease.
- Limited data exists on pediatric patients with mitochondrial disorders experiencing beta-blocker adverse effects.
Purpose of the Study:
- To report a case of respiratory distress in a pediatric patient with mitochondrial disorder potentially induced by metoprolol.
- To highlight the potential for aggravated mitochondrial dysfunction and chest wall weakness due to beta-blocker therapy in children.
Main Methods:
- A case report of a pediatric patient with a diagnosed mitochondrial disorder is presented.
- The patient developed respiratory distress after initiation of metoprolol for hypertension.
- Symptoms were evaluated, and metoprolol was discontinued; alternative etiologies were excluded.
Main Results:
- The pediatric patient experienced significant respiratory distress after starting metoprolol.
- Discontinuation of metoprolol led to improvement in respiratory symptoms.
- No other cause for the respiratory distress was identified.
Conclusions:
- Metoprolol may exacerbate mitochondrial dysfunction, leading to increased chest wall weakness and respiratory distress in pediatric patients.
- This case underscores the importance of cautious beta-blocker use in children with mitochondrial disorders.
- Further investigation into the impact of beta-blockers on pediatric mitochondrial myopathies is warranted.
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