Stroke risk in hypertrophic cardiomyopathy patients with atrial fibrillation: a nationwide database study

Jung-Chi Hsu1,2, Ya-Ting Huang3, Lian-Yu Lin2,4,5

  • 1Division of Cardiology, Department of Internal Medicine, Camillian Saint Mary’s Hospital Luodong, Yilan, Taiwan.

Aging
|November 23, 2020
PubMed

Insights

Current guidelines suggest anticoagulation for hypertrophic cardiomyopathy (HCM) with atrial fibrillation (AF) for all patients. However, this study found that young HCM patients with AF have a low stroke risk, suggesting anticoagulants may not be necessary for this group.

Area of Science:

  • Cardiology
  • Neurology
  • Epidemiology

Background:

  • Current guidelines recommend anticoagulation for hypertrophic cardiomyopathy (HCM) with atrial fibrillation (AF) irrespective of stroke risk scores.
  • Aging and common stroke risk factors may confound stroke risk assessment in HCM patients with AF.

Purpose of the Study:

  • To determine the incidence of stroke and identify its risk factors in Taiwanese patients with concomitant HCM and AF.
  • To evaluate the necessity of anticoagulation in younger HCM patients with AF.

Main Methods:

  • Retrospective analysis of a national database including 18,724 HCM patients from 1997 to 2013.
  • Estimation of AF and stroke incidence using Cox regression models.
  • Assessment of risk factors including age and CHA2DS2-VASc score.

Main Results:

  • AF incidence was 5.83 per 1000 person-years; AF-associated stroke incidence was 24.14 per 1000 person-years.
  • Stroke incidence varied and was not proportional to CHA2DS2-VASc score.
  • Age (HR 1.04) and prior TIA/ischemic stroke (HR 2.82) were independent predictors of stroke. No stroke occurred in patients <40 years.

Conclusions:

  • Taiwanese patients with HCM and AF face a high stroke risk, with age being the primary predictor, independent of the CHA2DS2-VASc score.
  • The low incidence of stroke in younger patients (<40 years) suggests that anticoagulation may not be required for this specific subpopulation.

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...
198
Acute Coronary Syndrome III: Diagnostic Studies01:30

Acute Coronary Syndrome III: Diagnostic Studies

Diagnosing acute coronary syndrome or ACS begins with a thorough patient history. Notable symptoms include central, crushing chest pain radiating to the left arm, neck, jaw, or back, along with shortness of breath, sweating (diaphoresis), nausea, vomiting, dizziness, and palpitations.It is crucial to note any history of cardiac illnesses and assess risk factors, including age, gender, smoking, hypertension, diabetes, hyperlipidemia, and a sedentary lifestyle.During physical examination, vital...
107
Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies01:22

Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies

The key clinical manifestations of Rheumatic heart disease (RHD) include several distinct cardiac symptoms.Carditis, a hallmark of acute rheumatic fever, involves inflammation of the heart's endocardium, myocardium, and pericardium. Chronic RHD often results from recurrent episodes of carditis. Its symptoms include the following:Murmurs are caused by valvular damage, especially to the mitral and aortic valves. Mitral stenosis or regurgitation is common, with characteristic heart murmurs...
263