Fabry disease cardiomyopathy: Time for a closer heart rhythm monitoring?

Giacomo Mugnai1,2, Davide Genovese3, Laura De Michieli4

  • 1Division of Cardiology, Cardio-Thoracic Department, University Hospital of Verona, Verona, Italy. mugnai.giacomo@gmail.com.

Heart Failure Reviews
|July 15, 2026
PubMed

Insights

Anderson-Fabry disease (FD) patients face high sudden cardiac death (SCD) risk. Continuous monitoring, guided by fibrosis and hypertrophy, is crucial for identifying high-risk individuals and preventing lethal arrhythmias.

Area of Science:

  • Cardiology
  • Genetics
  • Electrophysiology

Background:

  • Cardiovascular disease is the primary cause of mortality in Anderson-Fabry disease (FD).
  • Sudden cardiac death (SCD) is a frequent cause of mortality in FD patients.
  • Current risk stratification tools inadequately predict lethal arrhythmic events in FD.

Purpose of the Study:

  • To review the pathophysiology of FD-related arrhythmias.
  • To evaluate diagnostic limitations of current monitoring tools.
  • To propose an updated risk-stratification guide for continuous rhythm monitoring in high-risk FD subgroups.

Main Methods:

  • Narrative review of peer-reviewed literature.
  • Analysis of observational and registry data.
  • Evaluation of diagnostic limitations of 24-hour Holter monitoring versus implantable loop recorders (ILRs).

Main Results:

  • Standard monitoring tools often miss paroxysmal, asymptomatic arrhythmias in FD.
  • ILRs reveal a higher burden of arrhythmias than previously recognized.
  • Myocardial fibrosis (LGE on CMR) and left ventricular hypertrophy (LVH) are associated with malignant arrhythmias.

Conclusions:

  • Current consensus may underestimate the need for continuous monitoring in FD.
  • Myocardial fibrosis and LVH are key indicators for arrhythmia risk.
  • An updated risk-stratification guide is proposed to extend continuous monitoring in high-risk FD patients.

Related Concept Videos

Pulse rhythm01:30

Pulse rhythm

Pulse rhythm refers to the pattern of pulsations within specific intervals, offering valuable insights into the regularity or irregularity of the heart's beats as observed through the pattern of pulsation within specific intervals. A regular pulse exhibits a consistent heart rate with uniform waveforms and pulsation force, variations of which can be classified as normal, weak, or bounding.
Conversely, an irregular pulse pattern is termed dysrhythmia, stemming from disruptions in cardiac muscle...
Dysrhythmias V: Evaluating Dysrhythmias01:30

Dysrhythmias V: Evaluating Dysrhythmias

Dysrhythmias, also known as arrhythmias, are disturbances in the heart's rhythm that range from benign to life-threatening. A thorough evaluation is crucial for appropriate management and involves a comprehensive medical history, physical examination, and various diagnostic tests.Medical HistorySymptoms: Collect detailed information on palpitations, dizziness, syncope, chest pain, and fatigue. Note their onset, frequency, and triggers.Previous Cardiac Issues: Document any history of heart...
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 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...
Cardiomyopathy VI: Nursing Management01:29

Cardiomyopathy VI: Nursing Management

Assessment: Nursing management of patients with cardiomyopathy begins with a thorough assessment of the patient's history, including a family history of cardiomyopathy or sudden cardiac death, personal history of heart disease, hypertension, diabetes, and any alcohol consumption or drug use.During the physical examination, assess vital signs, look for signs of heart failure (such as edema, jugular venous distention, and cyanosis), auscultate for abnormal heart sounds (like murmurs and gallops),...
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...