© Rob3000 | Dreamstime.com
Cardiomyopathy is sometimes referred to as an “enlarged heart,” because the main sign is a heart muscle that has become thicker and more rigid. Bigger muscles might be what athletes want in their arms and legs. But a bigger heart isn’t a good thing, as it actually becomes weaker rather than stronger.
Unfortunately, there often aren’t obvious enlarged heart symptoms when the condition is first developing. But some enlarged heart causes, including symptoms of heart attack, bear unmistakable signs.
Prevent a heart attack, reduce your stroke risk, and lower your blood pressure. Avoid medications, when possible—even avoid doctor and hospital visits!
Maintain a healthy heart by claiming, right now, your FREE copy of our definitive guide to avoiding heart disease and taking care of your ticker.
There are actually several different types of cardiomyopathy. They include the following:
- Hypertrophic cardiomyopathy: An enlargement of the heart muscle without an obvious cause.
- Dilated cardiomyopathy: An enlargement and weakening of the ventricles, which can lead to heart failure, arrhythmias and blood clots.
- Restrictive cardiomyopathy: Reduced blood volume filling the ventricles, which become stiff but not thick.
- Arrhythmogenic right ventricular dysplasia: A rare but serious disease in which the right ventricle’s muscle is replaced with more fibrous and fatty tissue. It often leads to arrhythmias.
There are other types of cardiomyopathy, usually categorized under “unclassified cardiomyopathy.” Some people with mild cardiomyopathy may never experience any enlarged heart symptoms, while others develop very serious complications. Typically, the cause of your cardiomyopathy determines the severity of symptoms and the type of treatment that you’ll need.
There are two basic enlarged heart causes. It can either be inherited or acquired. Inherited, as you might surmise, means the condition is part of the genes passed on to you from your parents. Hypertrophic cardiomyopathy is often inherited, though it can develop in older adults.
Dilated cardiomyopathy is sometimes inherited, but is usually the result of coronary artery disease, high blood pressure, a heart attack, or other heart condition. A viral infection that causes inflammation of the heart can also lead to dilated cardiomyopathy. The condition in women is also sometimes related to complications during the last months of pregnancy.
Causes of an Enlarged Heart
The causes of restrictive cardiomyopathy range from connective tissue disorders, such as Marfan syndrome and cellulitis, to cancer treatments, such as chemotherapy and radiation. Other health problems, such as amyloidosis (a buildup of certain proteins in the heart and other organs), can also result in restrictive cardiomyopathy.
Arrhythmogenic right ventricular dysplasia is thought to be an inherited enlarged heart cause.
In the early stages of cardiomyopathy, you may not notice any enlarged heart symptoms. But as the condition develops, you may experience heart failure-like symptoms, such as shortness of breath, fatigue, and swelling in the legs and feet (and possibly in the neck and abdomen). Dizziness or lightheadedness may also occur, and arrhythmias may also develop over time.
See also these University Health News posts on heart health:
- “The Four Heart Problem Symptoms You Shouldn’t Ignore“
- “Fluttering, Pounding, Skipping a Beat. . . What Do Heart Palpitations Symptoms Mean?“
- “Mild Heart Attack Symptoms: What Do They Mean?“
Originally published in April 2016 and updated.