Most common form of cardiomyopathy, characterised by ventricular chamber enlargement and contractile dysfunction with normal left ventricular wall thickness
Aetiology
Familial DCM is associated with mutations in genes responsible for cytoskeleton or proteins involved in contractions; it is predominantly autosomal dominant
Sporadic DCM can be caused by multiple conditions:
Toxins e.g. drugs, alcohol, chemotherapy (doxorubicin)
Myocarditis
Autoimmune disorders
Endocrine disorders
Neuromuscular disorders
Pathophysiology
DCM is characterized by enlarged ventricular size, with normal ventricular wall thickness and systolic dysfunction
Heart becomes ‘floppy’ with reduced ejection fraction
Clinical presentation
Heart failure - dyspnoea, pulmonary oedema etc.
Cardiac arrhythmias
Conduction defects
Thromboembolism
Sudden death
Investigations
ECG - ST-segment and T wave changes
Echocardiogram - dilation of left and/or right ventricle with poor contraction function