Heart disease a leading cause of death globally. It encompasses a range of conditions that affect the heart.
Heart diseases include:
- Blood vessel disease, such as coronary artery disease.
- Irregular heartbeats (arrhythmias).
- Heart problems you’re born with (congenital heart defects).
- Disease of the heart muscle.
- Heart valve disease
In This Article
ToggleSymptoms
Heart disease symptoms depend on the type of heart disease.
CORONARY ARTERY DISEASE
Coronary artery disease (CAD) is a common type of heart disease. It occurs when the blood vessels that supply blood to the heart muscle become narrowed or blocked due to a buildup of plaque. The plaque is made up of cholesterol, fat, and other substances. This buildup restricts blood flow to the heart. This leads to various symptoms such as chest pain (angina), shortness of breath, and in severe cases, heart attack.
Risk factors for coronary artery disease
- High blood pressure (hypertension): Increases the workload on the heart and damages the arteries over time.
- High cholesterol levels: High levels of LDL cholesterol (“bad” cholesterol) can lead to plaque buildup in the arteries.
- Smoking: Damages the lining of the arteries and contributes to plaque buildup.
- Diabetes: Increases the risk of developing CAD, as high blood sugar levels can damage the arteries.
- Obesity: Excess weight puts strain on the heart and is often associated with other risk factors like high blood pressure and diabetes.
- Family history: Having close relatives with CAD increases your risk.
- Sedentary lifestyle: Lack of physical activity can contribute to obesity and other risk factors.
Symptoms of coronary artery disease
The symptoms can vary depending on the severity of the condition. Some common symptoms include:
- Chest pain or discomfort (angina): This is the most common symptom of CAD. Chest pain may feel like pressure, squeezing, fullness, or pain in the chest. It can also radiate to the arms, shoulders, neck, jaw, or back. Pain in the chest typically occurs during physical activity or emotional stress and is relieved by rest or medication.
- Shortness of breath: CAD can cause shortness of breath, especially during physical exertion or when lying flat.
- Fatigue: Feeling tired or lacking energy is a common symptom of CAD. The heart may not be able to pump blood effectively.
- Weakness: CAD can cause weakness, particularly in the arms and legs. This is due to reduced blood flow to the muscles.
- Nausea: Some people with CAD may experience nausea, indigestion, or vomiting, especially in women.
- Sweating: Unexplained sweating, particularly cold sweats, can be a symptom of CAD.
- Dizziness or lightheadedness: Reduced blood flow to the brain can cause dizziness or lightheadedness.
It’s important to note that some people with CAD may not experience any symptoms, especially in the early stages of the disease. This is known as silent ischemia and can increase the risk of a heart attack without warning. If you experience any symptoms of CAD, it’s essential to see a doctor for evaluation and appropriate management.
Arrhythmias
Arrhythmias are abnormalities in the heart’s rhythm or rate. They which can cause the heart to beat too fast, too slow, or irregularly. The heart has its natural pacemaker, the sinoatrial (SA) node, which sends electrical signals to control the heart’s rhythm. When these signals are disrupted or originate from abnormal locations, arrhythmias can occur.
Types of arrhythmias
- Atrial fibrillation (AFib): This is the most common type of arrhythmia. It is where the heart’s upper chambers (atria) quiver instead of contracting effectively. AFib can lead to blood clots, stroke, heart failure, and other complications.
- Bradycardia: This is when the heart rate is slower than normal (usually less than 60 beats per minute). Bradycardia may not cause symptoms if the heart is still pumping enough blood. However, it can lead to fatigue, dizziness, fainting, or even cardiac arrest.
- Tachycardia: This is when the heart rate is faster than normal (usually more than 100 beats per minute). Tachycardia can be further classified into different types. They include supraventricular tachycardia (SVT) and ventricular tachycardia (VT). SVT originates above the ventricles and may cause symptoms such as palpitations, dizziness, or fainting. VT originates in the ventricles and can be life-threatening if not treated promptly.
- Premature contractions: These are extra, abnormal heartbeats that can occur in the atria (premature atrial contractions or PACs) or ventricles (premature ventricular contractions or PVCs). They are usually harmless but can sometimes cause palpitations or other symptoms.
- Heart block: This occurs when the electrical signals between the heart’s upper and lower chambers are delayed or blocked. Heart block can range from mild to severe and may cause symptoms such as fatigue, dizziness, fainting, or chest pain.
Symptoms of arrhythmias
Arrhythmias can manifest in various ways, depending on the type and severity of the condition. Some common symptoms of arrhythmias include:
- Palpitations: This is an awareness of the heartbeat, often described as a fluttering, pounding, or racing sensation in the chest. Palpitations can occur with different types of arrhythmias and may be intermittent or persistent.
- Dizziness or lightheadedness: Arrhythmias can disrupt blood flow to the brain, leading to feelings of dizziness, lightheadedness, or fainting (syncope).
- Shortness of breath: In some cases, arrhythmias can cause difficulty breathing, especially during physical activity or when lying flat.
- Chest pain or discomfort: Certain arrhythmias, particularly those associated with ischemic heart disease, may cause chest pain or discomfort similar to angina.
- Fatigue or weakness: Arrhythmias can impair the heart’s ability to pump blood effectively, leading to feelings of fatigue, weakness, or reduced exercise tolerance.
- Fluttering sensation in the neck or throat: Some people may feel a fluttering sensation in their neck or throat when experiencing certain types of arrhythmias, such as atrial fibrillation.
- Anxiety or panic: Arrhythmias can sometimes trigger feelings of anxiety or panic, especially if they are accompanied by palpitations or other symptoms.
- Fainting or near-fainting episodes: Severe arrhythmias, particularly those causing significant reductions in blood flow, may result in fainting or near-fainting episodes (presyncope).
It’s important to note that some arrhythmias may not cause any symptoms, especially if they are brief or occur infrequently. However, even asymptomatic arrhythmias can increase the risk of serious complications such as stroke or sudden cardiac arrest. If you experience any symptoms suggestive of an arrhythmia, it’s essential to see a doctor for evaluation and appropriate management.
Treatment for arrhythmias
Treatment depends on the type and severity of the condition. It may include medications, lifestyle changes, medical procedures such as cardioversion or ablation, or implantable devices like pacemakers or defibrillators. Managing underlying conditions such as heart disease, high blood pressure, or thyroid disorders is also important in preventing or controlling arrhythmias. If you suspect you have an arrhythmia or experience symptoms such as palpitations, dizziness, or fainting, it’s essential to see a doctor for evaluation and appropriate management.
Congenital heart defects
Congenital heart defects (CHDs) are structural problems with the heart that are present at birth. These defects can affect the heart’s walls, valves, and blood vessels. They can vary greatly in severity, ranging from simple issues that may not require treatment to complex problems that require surgery.
Types of Congenital Heart Defects
- Septal Defects:
- Atrial Septal Defect (ASD): A hole in the wall (septum) that separates the upper chambers of the heart (atria).
- Ventricular Septal Defect (VSD): A hole in the wall separating the lower chambers of the heart (ventricles).
- Valve Defects:
- Pulmonary Valve Stenosis: Narrowing of the pulmonary valve.
- Aortic Valve Stenosis: Narrowing of the aortic valve.
- Tricuspid Atresia: Absence of the tricuspid valve, which leads to an underdeveloped right ventricle.
- Outflow Tract Obstructions:
- Coarctation of the Aorta: Narrowing of the aorta.
- Pulmonary Atresia: Absence of a connection between the right ventricle and the pulmonary artery.
- Complex Defects:
- Tetralogy of Fallot: A combination of four defects: VSD, pulmonary stenosis, right ventricular hypertrophy, and an overriding aorta.
- Transposition of the Great Arteries (TGA): The positions of the pulmonary artery and the aorta are switched.
- Hypoplastic Left Heart Syndrome: Underdevelopment of the left side of the heart.
Causes and Risk Factors
- Genetic Factors: Some CHDs are linked to genetic conditions, such as Down syndrome.
- Environmental Factors: Maternal health conditions (e.g., diabetes, obesity), medications, alcohol or drug use during pregnancy, and infections like rubella can increase the risk of CHDs.
- Unknown Causes: Many CHDs have no identifiable cause.
Symptoms
- Mild Defects: May have no symptoms and be detected during a routine check-up.
- Severe Defects:
Serious congenital heart defects usually are noticed soon after birth. Congenital heart defect symptoms in children could include:
- Pale gray or blue skin or lips (cyanosis)
- Swelling in the legs, belly area or areas around the eyes
- In an infant, shortness of breath during feedings, leading to poor weight gain
Less-serious congenital heart defects are often not diagnosed until later in childhood or during adulthood. Symptoms of congenital heart defects that usually aren’t immediately life-threatening include:
- Easily getting short of breath during exercise or activity
- Easily tiring during exercise or activity
- Swelling of the hands, ankles or feet
- Symptoms can include rapid breathing, cyanosis (bluish skin), fatigue, poor feeding, and poor weight gain.
Diagnosis
- Prenatal Screening: Ultrasound during pregnancy can sometimes detect CHDs.
- Postnatal Diagnosis: Echocardiograms, chest X-rays, electrocardiograms (ECG), and cardiac catheterization can diagnose CHDs after birth.
Treatment
- Medications: To manage symptoms or complications.
- Catheter Procedures: Minimally invasive procedures to repair certain defects.
- Surgery: Some defects require open-heart surgery for correction.
- Heart Transplant: In severe cases, a heart transplant may be necessary.
Long-Term Outlook
With advances in medical care, many individuals with congenital heart defects can lead normal lives, though they may require ongoing medical care and monitoring. Regular follow-ups with a cardiologist specializing in congenital heart defects are often necessary.
Prevention and Management
- Prenatal Care: Proper prenatal care can help reduce the risk of CHDs.
- Healthy Lifestyle: Maintaining a healthy lifestyle during pregnancy.
- Genetic Counseling: For families with a history of CHDs or genetic conditions.
Disease of the heart muscle
Diseases of the heart muscle, known as cardiomyopathies, affect the heart’s ability to pump blood effectively. There are several types of cardiomyopathy, each with different causes and characteristics.
Types of Cardiomyopathy
- Dilated Cardiomyopathy (DCM)
- Description: The heart’s chambers enlarge and lose the ability to contract effectively.
- Causes: Can be genetic, due to infections (viral myocarditis), alcohol abuse, drugs, or exposure to toxins.
- Symptoms: Fatigue, shortness of breath, swelling of the legs, irregular heartbeats (arrhythmias).
- Hypertrophic Cardiomyopathy (HCM)
- Description: The heart muscle becomes abnormally thick, which can make it harder for the heart to pump blood.
- Causes: Often inherited genetically.
- Symptoms: May be asymptomatic or cause chest pain, dizziness, shortness of breath, and fainting, especially during exercise.
- Restrictive Cardiomyopathy (RCM)
- Description: The heart muscle becomes rigid and less elastic, preventing the heart from expanding properly and filling with blood between heartbeats.
- Causes: Can be idiopathic (unknown cause) or due to diseases like amyloidosis, sarcoidosis, or hemochromatosis.
- Symptoms: Shortness of breath, fatigue, swelling of the legs and feet, and arrhythmias.
- Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
- Description: The muscle tissue in the right ventricle is replaced with fatty or fibrous tissue, leading to arrhythmias.
- Causes: Often genetic.
- Symptoms: Palpitations, fainting, and in severe cases, sudden cardiac arrest.
- Unclassified Cardiomyopathies
- Description: Types that do not fit into the other categories or have unique features.
- Examples: Left ventricular noncompaction, takotsubo cardiomyopathy (stress-induced cardiomyopathy).
Causes and Risk Factors
- Genetic Factors: Many cardiomyopathies have a genetic component.
- Infections: Viral infections can cause myocarditis, leading to cardiomyopathy.
- Toxins and Alcohol: Chronic alcohol abuse and exposure to certain toxins can damage the heart muscle.
- Medical Conditions: Conditions such as diabetes, thyroid disorders, and hypertension can contribute to cardiomyopathy.
- Nutritional Deficiencies: Lack of essential nutrients, such as thiamine (vitamin B1), can lead to cardiomyopathy.
Symptoms
- General Symptoms: Fatigue, shortness of breath (especially with exertion or lying flat), swelling in the legs, ankles, and feet.
- Specific Symptoms: Depending on the type, symptoms may include chest pain, dizziness, fainting, palpitations, and irregular heartbeats.
Diagnosis
- Physical Examination: A doctor may detect abnormal heart sounds, fluid in the lungs, or swelling in the legs.
- Imaging: Echocardiogram, MRI, or CT scan to visualize the heart’s structure and function.
- Electrocardiogram (ECG): To detect irregular heart rhythms.
- Blood Tests: To check for underlying conditions or markers of heart damage.
- Genetic Testing: For inherited forms of cardiomyopathy.
Treatment
- Medications: To manage symptoms and prevent complications, such as beta-blockers, ACE inhibitors, diuretics, and antiarrhythmic drugs.
- Lifestyle Changes: Diet, exercise, avoiding alcohol and drugs, and managing underlying conditions.
- Devices: Pacemakers or implantable cardioverter-defibrillators (ICDs) for arrhythmias.
- Surgery: In severe cases, options include septal myectomy (for HCM) or heart transplant.
Prognosis
The outlook for individuals with cardiomyopathy varies based on the type, severity, and response to treatment. Many people can manage their symptoms and live a normal life with appropriate treatment and lifestyle changes.
Heart valve disease
Heart valve disease involves dysfunction of one or more of the heart’s four valves, which are responsible for ensuring blood flows in the correct direction through the heart. The four heart valves are the mitral valve, aortic valve, tricuspid valve, and pulmonary valve. Valve disease can lead to stenosis (narrowing) or regurgitation (leakage).
Types of Heart Valve Disease
- Mitral Valve Disease
- Mitral Stenosis: Narrowing of the mitral valve opening, impeding blood flow from the left atrium to the left ventricle.
- Mitral Regurgitation: The mitral valve does not close properly, causing blood to flow backward into the left atrium.
- Aortic Valve Disease
- Aortic Stenosis: Narrowing of the aortic valve, restricting blood flow from the left ventricle to the aorta.
- Aortic Regurgitation: The aortic valve does not close properly, allowing blood to flow backward into the left ventricle.
- Tricuspid Valve Disease
- Tricuspid Stenosis: Narrowing of the tricuspid valve, impeding blood flow from the right atrium to the right ventricle.
- Tricuspid Regurgitation: The tricuspid valve does not close properly, causing blood to flow backward into the right atrium.
- Pulmonary Valve Disease
- Pulmonary Stenosis: Narrowing of the pulmonary valve, restricting blood flow from the right ventricle to the pulmonary artery.
- Pulmonary Regurgitation: The pulmonary valve does not close properly, allowing blood to flow backward into the right ventricle.
Causes and Risk Factors
- Congenital Heart Defects: Some people are born with valve defects.
- Rheumatic Fever: Can cause scarring of the heart valves.
- Infections: Endocarditis (infection of the inner lining of the heart) can damage the valves.
- Age-Related Changes: Calcium deposits can build up on the valves, leading to stenosis.
- Other Conditions: Marfan syndrome, lupus, and other diseases can affect the valves.
Symptoms
- Shortness of Breath: Especially during activity or when lying down.
- Fatigue: Feeling unusually tired.
- Swelling: In the ankles, feet, or abdomen.
- Chest Pain: Particularly with aortic stenosis.
- Heart Murmurs: Abnormal heart sounds detected by a doctor.
- Palpitations: Irregular heartbeats or the sensation of a racing heart.
- Dizziness or Fainting: Often related to aortic stenosis or severe regurgitation.
Diagnosis
- Physical Examination: A doctor may hear a heart murmur or other abnormal sounds.
- Echocardiogram: Ultrasound imaging to visualize the heart valves and chambers.
- Electrocardiogram (ECG): To detect irregular heart rhythms.
- Chest X-Ray: To see the size and shape of the heart and detect fluid in the lungs.
- Cardiac MRI: Detailed images of the heart.
- Cardiac Catheterization: To measure pressures within the heart and assess the severity of valve disease.
Treatment
- Medications: To manage symptoms and prevent complications, such as diuretics, beta-blockers, ACE inhibitors, and anticoagulants.
- Lifestyle Changes: Healthy diet, regular exercise, and avoiding smoking and excessive alcohol.
- Valve Repair or Replacement: Surgical procedures to fix or replace damaged valves.
- Valve Repair: Techniques include valvuloplasty (balloon to widen a stenotic valve) or repairing the valve structure.
- Valve Replacement: Using mechanical or biological (tissue) valves.
- Transcatheter Valve Procedures: Minimally invasive procedures, such as TAVR (transcatheter aortic valve replacement), for high-risk patients.
Prognosis
The outlook for individuals with heart valve disease varies based on the type and severity of the disease, as well as the success of treatment. Many people can manage their symptoms and live a full life with appropriate treatment and regular follow-up care.