A cardiomyopathy is a disease of the myocardium which is not caused by coronary artery disease, hypertension, valvular disease or congenital heart diseases. In other words, myocardial diseases caused by hypertension, coronary artery disease, valvular disease or congenital heart diseases are not considered cardiomyopathies.

Some definitions include the aforementioned diseases as cardiomyopathies, but most definitions don’t.^[1]

Cardiomyopathies are either primary or secondary. Primary cardiomyopathies are caused by diseases that only or prediminantly affect the myocardium. Idiopathic or genetic causes are usually in the background. Secondary cardiomypathies are caused by myocardial involvement in systemic diseases.

We distinguish four types of cardiomyopathy: Dilatative, hypertrophic, restrictive and arrhythmogenic right ventricular cardiomyopathy. Each of them can have two types of causes: primary and secondary.

Dilatative cardiomyopathy

Dilatative cardiomyopathy is the most common cardiomyopathy. It’s characterised by dilation and impaired contraction of one or both ventricles. In dilatative cardiomyopathy the ventricular wall is continuously thinning, which increases the lumen of the ventricle. It leads to a decrease in ejection fraction with a decreased cardiac output, eventually causing heart failure.

It’s primary in 50% of cases, which is idiopathic. There are probably some genetic components.

Secondary causes of dilatative cardiomyopathy:

Pregnancy
Beri beri (Thiamine deficiency)
Coxsackie B myocarditis
Alcohol abuse
Cocaine abuse
Rheumatic heart disease
SLE

Hypertrophic cardiomyopathy

In hypertrophic cardiomyopathy the left ventricleis abnormally hypertrophic. The primary type is more common than the secondary type. There are two types:

Non-obstructive type – where the septum is not hypertrophic
Obstructive type – where the septum is hypertrophic

In the obstructive type the septum can be so hypertrophic that it obstructs the outflow tract of the left ventricle, completely ceasing cardiac output. This is a common cause of sudden cardiac death in young people.

In both types the hypertrophic ventricle has reduced compliance, so a high EDp is required to fill it. The contraction force is high, yielding an ejection fraction of almost 100%! The obstructive type is the worst of the two.

Primary hypertrophic cardiomyopathy is caused by mutations in the genes for the myosin heavy chain. It follows an autosomal dominant inheritance pattern.

Secondary hypertrophic cardiomyopathy has the following causes:

Friedreich’s Ataxia
Pompe’s disease

Restrictive cardiomyopathy

Restrictive cardiomyopathy is very rare. Something causes proliferation of connective tissue in the myocardium, which causes the ventricular wall to become restrictive and lose compliance. When the walls are stiff the EDp must be high to fill the ventricle, which causes backward venous congestion.

It’s mostly caused by secondary causes like:

Amyloidosis
Sarcoidosis
Hemochromatosis

Arrhythmogenic right ventricular cardiomyopathy

This is another rare type of cardiomyopathy. It’s characterized by a fatty or fibrotic degeneration of the right ventricle, causing the ventricular wall to become thinner and the ventricle itself to become dilated. As the name implies arrhythmias often occur.

It can cause sudden cardiac death in healthy young people due to lethal arrhythmias.

Only primary, idiopathic causes are known.

↑ https://www.uptodate.com/contents/definition-and-classification-of-the-cardiomyopathies

[1] ttps://www.uptodate.com/contents/definition-and-classification-of-the-cardiomyopathies

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