Obstructive sleep apnea and hypertrophic cardiomyopathy: a common and potential harmful combination

Flávia B Nerbass1, Rodrigo P Pedrosa, Naury J Danzi-Soares

  • 1Sleep Laboratory, Pulmonary Division, Heart Institute (InCor), University of São Paulo School of Medicine, Brazil.

Sleep Medicine Reviews
|October 11, 2012
PubMed

Insights

Obstructive sleep apnea (OSA) is highly prevalent in hypertrophic cardiomyopathy (HCM) patients, significantly worsening heart function and increasing atrial fibrillation risk. Early OSA detection may improve cardiovascular outcomes in HCM.

Area of Science:

  • Cardiology
  • Sleep Medicine
  • Genetics

Background:

  • Hypertrophic cardiomyopathy (HCM) is a common genetic heart disease leading to significant disability and mortality.
  • Obstructive sleep apnea (OSA) is prevalent in cardiovascular disease and may worsen outcomes.
  • Patients with HCM often lack typical OSA risk factors like obesity.

Purpose of the Study:

  • To investigate the prevalence and impact of OSA in patients diagnosed with HCM.
  • To explore the association between OSA and cardiac structural/functional changes in HCM.
  • To determine if OSA influences the risk of atrial fibrillation in HCM patients.

Main Methods:

  • Systematic review and meta-analysis of studies reporting OSA prevalence in HCM patients.
  • Analysis of cardiac parameters, functional class, and quality of life in HCM patients with and without OSA.
  • Assessment of atrial fibrillation prevalence in HCM patients with and without OSA.

Main Results:

  • OSA prevalence in HCM patients ranges from 32% to 71%.
  • OSA is independently linked to worse cardiac structure (atrial/aorta enlargement), functional class, and quality of life.
  • Atrial fibrillation prevalence is approximately four times higher in HCM patients with OSA.

Conclusions:

  • OSA is a common comorbidity in HCM patients, independent of typical risk factors.
  • The presence of OSA exacerbates cardiac impairment and increases atrial fibrillation risk in HCM.
  • Screening for OSA in HCM patients is crucial for potentially improving management and outcomes.

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Sleep Apnea01:21

Sleep Apnea

Sleep apnea is a condition where breathing stops intermittently during sleep, often leading to significant health issues. Each episode can last from 10 to 20 seconds or more and is frequently accompanied by a brief arousal from sleep. This disturbance, largely unnoticed by the individual, can lead to severe daytime fatigue. Commonly, individuals seek help after being informed by their partners about loud snoring and noticeable breathing pauses during sleep.
The condition is more prevalent among...
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Cardiomyopathy VII: Pre and Post Operative Nursing Management01:28

Cardiomyopathy VII: Pre and Post Operative Nursing Management

Patients with hypertrophic cardiomyopathy (HCM) and left ventricular outflow tract (LVOT) obstruction who remain symptomatic despite optimal medical therapy may undergo a septal myectomy (Morrow procedure). This procedure involves excising a portion of the hypertrophied septum below the aortic valve using a heart-lung machine to improve blood flow through the LVOT. Effective preoperative and postoperative nursing management ensures successful patient outcomes, minimizes complications, and...