Panelists discuss how recognizing key clinical manifestations and red flag symptoms, such as bilateral carpal tunnel syndrome, spinal stenosis, and trigger fingers, is critical for early diagnosis and intervention in patients with transthyretin amyloid cardiomyopathy (ATTR-CM), particularly in those with unexplained heart failure or arrhythmias.
Summary for Physicians: Clinical Manifestations and Red Flag Symptoms of ATTR-CM
Clinical Manifestations of ATTR-CM:
Cardiac symptoms:
Heart failure (HF), often with restrictive cardiomyopathy
Atrial arrhythmias that are resistant to ablation procedures
Bradyarrhythmias and tachyarrhythmias
Pacemaker dependence in advanced cases
Extracardiac symptoms:
Bilateral carpal tunnel syndrome (CTS): Often a key early sign of the disease
Spinal stenosis: May cause discomfort or neurological deficits
Trigger fingers: Common in patients with hereditary transthyretin amyloid cardiomyopathy (hATTR-CM)
Pulmonary embolism: Can occur in advanced stages
Electrocardiogram findings:
May show signs of low-voltage QRS complexes, heart block, or other arrhythmias typical of restrictive cardiomyopathy
Imaging:
Echocardiography and cardiac MRI often show characteristic features of restrictive cardiomyopathy or amyloid deposits.
Chest x-ray may show evidence of HF.
Laboratory findings:
Elevated biomarkers such as NT-proBNP and troponins can be seen in cardiac involvement.
Genetic testing can confirm the diagnosis of hATTR-CM.
Red Flag Symptoms for hATTR-CM:
Persistent bilateral CTS, spinal stenosis, and trigger fingers should raise suspicion of hATTR-CM, especially in patients with unexplained HF or arrhythmias.
A history of family members with similar symptoms or genetic mutations associated with ATTR-CM further supports the diagnosis.
Early recognition of these symptoms is essential for timely diagnosis and intervention in patients with ATTR-CM.