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Published on: December 6, 2016
Sleep-disordered breathing in hypertrophic cardiomyopathy: challenges and opportunities
Tomas Konecny1, Virend K Somers2
1Mayo Clinic, Rochester, MN; International Clinical Research Center, St Anne's Hospital, Brno, Czech Republic.
Insights
Sleep-disordered breathing is common in hypertrophic cardiomyopathy and may be a treatable risk factor. Addressing SDB could improve outcomes for HCM patients, highlighting a need for further research.
Area of Science:
- Cardiology
- Sleep Medicine
- Genetics
Background:
- Hypertrophic cardiomyopathy (HCM) is the most common inherited heart muscle disease.
- Sleep-disordered breathing (SDB) is increasingly recognized as a significant comorbidity.
- The link between SDB and adverse cardiovascular outcomes in HCM requires further elucidation.
Purpose of the Study:
- To review the pathophysiology of SDB in HCM.
- To explore the relationship between SDB and major cardiovascular events in HCM.
- To discuss clinical implications and identify research gaps.
Main Methods:
- Literature review and synthesis of existing evidence.
- Analysis of pathophysiological mechanisms linking SDB to cardiovascular disease.
- Discussion of clinical management strategies and future research directions.
Main Results:
- SDB is highly prevalent in patients with HCM.
- SDB is associated with hypertension, coronary artery disease, atrial fibrillation, and sudden cardiac death in HCM.
- Understanding these links is crucial for patient management.
Conclusions:
- SDB represents a potentially modifiable risk factor in HCM.
- Integrated care addressing both HCM and SDB is warranted.
- Further research is needed to optimize SDB screening and treatment in HCM.
Abstract:
Sleep-disordered breathing (SDB) may be a treatable risk factor in patients with hypertrophic cardiomyopathy (HCM), the most common inherited cardiomyopathy. Evidence suggests a high prevalence of SDB in HCM. We summarize the pathophysiology of SDB as it relates to hypertension, coronary artery disease, atrial fibrillation, and sudden cardiac death in patients with HCM. The implications regarding the care of patients with HCM and SDB are discussed as well as the knowledge deficits needing further exploration.
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