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Hypertrophic Cardiomyopathy


Tisha Suboc

, MD, Rush University

Reviewed/Revised Nov 2022
Topic Resources

Hypertrophic cardiomyopathy is a congenital or acquired disorder characterized by marked ventricular hypertrophy with diastolic dysfunction (eg, due to valvular aortic stenosis, coarctation of the aorta, systemic hypertension). Symptoms include dyspnea, chest pain, syncope, and sudden death. A systolic murmur, increased by Valsalva maneuver, is typically present in the hypertrophic obstructive type. Diagnosis is by echocardiography or cardiac MRI. Treatment is with beta-blockers, verapamil, disopyramide, mavacamten, and sometimes chemical reduction or surgical removal of outflow tract obstruction.

Etiology of Hypertrophic Cardiomyopathy

Pathophysiology of Hypertrophic Cardiomyopathy

The myocardium is abnormal with cellular and myofibrillar disarray, although this finding is not specific for hypertrophic cardiomyopathy.

In the most common phenotype, the anterior septum and contiguous anterior free wall below the aortic valve are markedly hypertrophied and thickened, with little or no hypertrophy of the left ventricular (LV) posterior wall. Sometimes isolated apical hypertrophy occurs; however, virtually any asymmetric pattern of left ventricular hypertrophy can be observed, and in a small minority of patients even symmetric hypertrophy has been noted.

About two thirds of patients exhibit obstructive physiology at rest or during exercise. Obstruction is the result of mechanical impedance to LV outflow during systole due to systolic anterior motion (SAM) of the mitral valve. During this process (SAM), the mitral valve and valve apparatus are sucked into the LV outflow tract by a Venturi effect of high-velocity blood flow, resulting in obstruction of flow and decrease in cardiac output. Mitral regurgitation can also occur as the result of distortion of leaflet motion by SAM of the mitral valve. This obstruction and valvular regurgitation contribute to the development of symptoms related to heart failure. Less commonly, midventricular hypertrophy leads to an intracavitary gradient at the papillary muscle level, rarely resulting in increased LV wall stress and increased risk of LV apical aneurysm.

Contractility is grossly normal, resulting in a normal ejection fraction (EF). Later, EF is elevated because the ventricle has a small volume and empties nearly completely to maintain cardiac output.

Hypertrophy results in a stiff, noncompliant chamber (usually the left ventricle) that resists diastolic filling, elevating end-diastolic pressure and thus increasing pulmonary venous pressure. As resistance to filling increases, cardiac output decreases, an effect worsened by any outflow tract gradient present. Because tachycardia allows less time for filling, symptoms tend to appear mainly during exercise or tachyarrhythmias. (See also Heart failure with preserved ejection fraction Heart failure with preserved ejection fraction (HFpEF) Heart failure (HF) is a syndrome of ventricular dysfunction. Left ventricular (LV) failure causes shortness of breath and fatigue, and right ventricular (RV) failure causes peripheral and abdominal... read more Heart failure with preserved ejection fraction (HFpEF) .)

In some cases, myocytes gradually die, probably because capillary/myocyte imbalance causes chronic diffuse ischemia. As myocytes die, they are replaced by diffuse fibrosis. Then, the hypertrophied ventricle with diastolic dysfunction gradually dilates and systolic dysfunction develops.

Symptoms and Signs of Hypertrophic Cardiomyopathy

Typically, symptoms appear between ages 20 and 40 and are exertional, but symptoms may be highly variable. They include dyspnea, chest pain (usually resembling typical angina Angina Pectoris Angina pectoris is a clinical syndrome of precordial discomfort or pressure due to transient myocardial ischemia without infarction. It is typically precipitated by exertion or psychologic stress... read more ), palpitations, and syncope Syncope Syncope is a sudden, brief loss of consciousness with loss of postural tone followed by spontaneous revival. The patient is motionless and limp and usually has cool extremities, a weak pulse... read more . Because systolic function is preserved, fatigability is seldom reported. The abnormal diastolic function is responsible for most symptoms. In patients with outflow tract obstruction, differentiation of symptoms due to the obstruction versus those caused by abnormal diastolic function can be difficult.

Syncope may occur during exertion either because outflow obstruction worsens with increased contractility or because of ventricular or atrial arrhythmia. Syncope is a marker of increased risk of sudden death.

Blood pressure and heart rate are usually normal, and signs of increased venous pressure are rare. When the outflow tract is obstructed, the carotid pulse has a brisk upstroke, bifid peak, and rapid downstroke. The apex beat may have a sustained thrust due to LV hypertrophy. A 4th heart sound (S4) is often present and is associated with a forceful atrial contraction against a poorly compliant left ventricle in late diastole.

In patients with the obstructive form of hypertrophic cardiomyopathy, a systolic ejection-type murmur can be heard that does not radiate to the neck. This murmur is heard best at the left sternal edge in the 3rd or 4th intercostal space. A mitral regurgitation murmur due to distortion of the mitral apparatus may be heard at the apex. The left ventricular outflow ejection murmur of hypertrophic cardiomyopathy can be increased by a Valsalva maneuver (which reduces venous return and LV diastolic volume), measures to lower aortic pressure (eg, nitroglycerin), or a postextrasystolic contraction (which increases the outflow tract pressure gradient). Handgrip increases aortic pressure, thereby reducing the murmur’s intensity.

Diagnosis of Hypertrophic Cardiomyopathy

  • Clinical suspicion (syncope, other symptoms, or murmur)

  • Echocardiography and/or MRI

Diagnosis is suspected based on a typical murmur and symptoms. Suspicion is increased if the patient has a history of unexplained syncope or a family history of unexplained sudden death. Unexplained syncope in young athletes should always raise suspicion. Hypertrophic cardiomyopathy must be distinguished from aortic stenosis and coronary artery disease, which cause similar symptoms. Less common infiltrative cardiac disorders such as Anderson-Fabry disease and amyloid heart disease may mimic findings of hypertrophic cardiomyopathy.

ECG and 2-dimensional echocardiography and/or MRI (the best noninvasive confirmatory tests) are done. Chest x-ray is often done but is usually normal because the ventricles are not dilated (although the left atrium may be enlarged). Patients with syncope or sustained arrhythmias should be evaluated as inpatients. Exercise testing and 24-hour ambulatory monitoring may be helpful for patients considered at high risk, although accurately identifying such patients is difficult.

The ECG Electrocardiography The standard electrocardiogram (ECG) provides 12 different vector views of the heart’s electrical activity as reflected by electrical potential differences between positive and negative electrodes... read more usually shows voltage criteria for LV hypertrophy (eg, S wave in lead V1 plus R wave in lead V5 or V6 > 35 mm). Very deep septal Q waves in leads I, aVL, V5, and V6 are often present with asymmetric septal hypertrophy; hypertrophic cardiomyopathy sometimes produces a QRS complex in V1 and V2, simulating previous septal infarction. T waves are usually abnormal; the most common finding is deep symmetric T-wave inversion in leads I, aVL, V5, and V6. ST-segment depression in the same leads is common (particularly in the apical obliterative form). The P wave is often broad and notched in leads II, III, and aVF, with a biphasic P wave in leads V1 and V2, indicating left atrial hypertrophy. Incidence of preexcitation phenomenon of the Wolff-Parkinson-White syndrome Reentrant Supraventricular Tachycardias (SVT) Including Wolff-Parkinson-White Syndrome Reentrant supraventricular tachycardias (SVT) involve reentrant pathways with a component above the bifurcation of the His bundle. Patients have sudden episodes of palpitations that begin and... read more type, which may cause palpitations, is increased. Bundle branch block Bundle Branch Block and Fascicular Block Bundle branch block is partial or complete interruption of impulse conduction in a bundle branch; fascicular block is similar interruption in a hemifascicle of the left bundle. The disorders... read more is common.

Two-dimensional Doppler echocardiography can differentiate the forms of cardiomyopathy (see figure Forms of cardiomyopathy Forms of cardiomyopathy Forms of cardiomyopathy ) and quantify the severity of hypertrophy and degree of outflow tract obstruction . These measurements are particularly useful for monitoring the effect of medical or surgical treatment. Midsystolic closure of the aortic valve sometimes occurs when outflow tract obstruction is severe. Ambulatory 24-hour monitoring is recommended during the initial evaluation and every 1 to 2 years to assess risk of sudden cardiac death and help guide treatment of arrhythmias.

Cardiac catheterization is usually done only when invasive therapy is considered. Usually, no significant stenoses are present in the coronary arteries, but older patients may have coexisting CAD.

Genetic markers do not influence treatment or identify high-risk individuals. However, genetic testing may be of benefit in screening family members.

Prognosis for Hypertrophic Cardiomyopathy

Overall, annual mortality is about 1% for adults but is higher for children. Death is usually sudden, and sudden death is the most common sequelae; chronic heart failure occurs less often. A higher risk of sudden cardiac death is predicted by the presence of the following risk factors:

  • Family history of sudden cardiac death due to hypertrophic cardiomyopathy, cardiac arrest, or sustained ventricular arrhythmias

  • Personal history of unexplained syncope, cardiac arrest, or sustained ventricular arrhythmias

  • Multiple repetitive non-sustained ventricular tachycardia (on ambulatory ECG)

  • Massive left-ventricular hypertrophy (thickness ≥ 30 mm), LV dysfunction (EF < 50%) , LV apical aneurysm

  • Extensive and diffuse late gadolinium enhancement on MRI

Treatment of Hypertrophic Cardiomyopathy

  • Beta-blockers

  • Rate-limiting and negative inotropic calcium channel blockers

  • Mavacamten

  • Avoidance of nitrates, diuretics, and angiotensin-converting enzyme (ACE) inhibitors

  • Possibly antiarrhythmics (eg, disopyramide, amiodarone)

  • Possibly implantable cardioverter-defibrillator and sometimes surgery or ablative procedures

Treatment of hypertrophic cardiomyopathy is based on the phenotype. Patients without obstruction generally have a stable clinical course without significant symptoms, although some experience heart failure symptoms due to diastolic dysfunction. Beta-blockers and heart rate-limiting calcium channel blockers with a lower arterial dilation capacity (usually verapamil), alone or combined, are the mainstays. By slowing the heart rate, they prolong the diastolic filling period, which may increase left ventricular filling in patients with diastolic dysfunction. Long-term efficacy of such therapy, however, has not been proven.

In patients with the obstructive phenotype, in addition to attempts at improving diastolic function, treatment is directed at reducing the outflow tract gradient. Non-dihydropyridine calcium channel blockers (eg, verapamil, diltiazem), beta-blockers, and disopyramide reduce the outflow tract gradient through their negative inotropic effects. Disopyramide appears to be most effective for patients with a resting gradient whereas beta-blockers are best at blunting the gradient that occurs during exercise. Beta-blockers are generally considered first-line treatment for patients with the obstructive phenotype; disopyramide helps relieve symptoms for patients who have failed first-line therapy with beta-blockers, verapamil, or diltiazem

Patients who continue to experience symptoms related to significant outflow tract gradients (≥ 50 mm Hg) despite medical therapy are candidates for invasive treatment. When done at an experienced center, surgical myectomy has a low operative mortality with excellent outcomes, making it the preferred therapy in such patients. Percutaneous catheter alcohol septal ablation is an alternative to surgery in older patients and others who are at high surgical risk.

Drugs that reduce preload (eg, nitrates, diuretics, ACE inhibitors, angiotensin II receptor blockers) decrease chamber size and worsen symptoms and signs. Vasodilators increase the outflow tract gradient and cause a reflex tachycardia that further worsens ventricular diastolic function. Inotropic drugs (eg, digitalis glycosides, catecholamines) worsen outflow tract obstruction, do not relieve the high end-diastolic pressure, and may induce arrhythmias. Mavacamtem, an oral cardiac myosin inhibitor that reduces actin-myosin cross-bridge formation, has been shown to relieve symptoms, reduce left ventricular outflow tract (LVOT) obstruction, and increase exercise tolerance in patients with hypertrophic cardiomyopathy (1, 2 Treatment references Hypertrophic cardiomyopathy is a congenital or acquired disorder characterized by marked ventricular hypertrophy with diastolic dysfunction (eg, due to valvular aortic stenosis, coarctation... read more Treatment references ).

If syncope or sudden cardiac arrest has occurred or if sustained ventricular arrhythmia is confirmed by ECG or 24-hour ambulatory monitoring, an implantable cardioverter-defibrillator Device therapy Heart failure (HF) is a syndrome of ventricular dysfunction. Left ventricular (LV) failure causes shortness of breath and fatigue, and right ventricular (RV) failure causes peripheral and abdominal... read more Device therapy (ICD) should usually be placed. Controversy exists regarding the need to place a defibrillator in patients without syncope, sudden cardiac arrest, or ventricular arrhythmias. It is generally believed that ICD insertion should be considered in patients with high-risk features (3 Treatment references Hypertrophic cardiomyopathy is a congenital or acquired disorder characterized by marked ventricular hypertrophy with diastolic dysfunction (eg, due to valvular aortic stenosis, coarctation... read more Treatment references ). High-risk features include

  • A family history of premature sudden cardiac arrest

  • Left ventricular wall thickness > 3 cm

  • Delayed enhancement on cardiac MRI

  • Unexplained syncope

  • Survival after a cardiac arrest due to ventricular arrhythmia

  • Multiple burst of nonsustained ventricular tachycardia (NSVT)

  • Left ventricular ejection fraction (LVEF) < 50% (end-stage disease)

  • Left ventricular aneurysm

Myomectomy and alcohol ablation have been used to decrease outflow obstruction and relive symptoms. There is no proven difference between these interventions on mortality, but myomectomy is more effective for relieving obstruction and decreasing the need for repeat interventions (4 Treatment references Hypertrophic cardiomyopathy is a congenital or acquired disorder characterized by marked ventricular hypertrophy with diastolic dysfunction (eg, due to valvular aortic stenosis, coarctation... read more Treatment references ).

Avoidance of competitive sports was previously recommended because sudden deaths can occur during increased exertion. Current guidelines recommend that athletes with HCM undergo comprehensive evaluation and shared discussion of potential risk with an expert HCM specialist.

Genetic counseling is appropriate for patients with asymmetric septal hypertrophy.

Treatment references

  • 1. Olivotto I, Oreziak A, Barriales-Villa R, et al: Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet 396:759–769, 2020.

  • 2. Spertus JA, Fine JT, Elliott P, et al: Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): health status analysis of a randomized, double-blind, placebo-controlled, phase 3 trial. Lancet 397:2467–2475, 2012. doi: 10.1016/S0140-6736(21)00763-7

  • 3. Maron MS, Rowin EJ, Wessler BS, et al: Enhanced American College of Cardiology/American Heart Association Strategy for Prevention of Sudden Cardiac Death in High-Risk Patients With Hypertrophic Cardiomyopathy. JAMA Cardiol 4(7):644–657, 2019. doi:10.1001/jamacardio.2019.1391

  • 4. Nguyen A, Schaff HV, Hang D, et al: Surgical myectomy versus alcohol septal ablation for obstructive hypertrophic cardiomyopathy: A propensity score-matched cohort. J Thorac Cardiovasc Surg 157(1):306–315.e3, 2019. doi:10.1016/j.jtcvs.2018.08.062

Key Points

  • Hypertrophic cardiomyopathy is usually due to one of numerous genetic mutations that cause various types of ventricular hypertrophy that restrict filling (ie, cause diastolic dysfunction) and sometimes obstruct LV outflow.

  • Coronary blood flow may be impaired even in the absence of coronary artery atherosclerosis because capillary density is inadequate and the intramyocardial coronary arteries are narrowed by intimal and medial hyperplasia and hypertrophy

  • At a young age, patients may have chest pain, dyspnea, palpitations, syncope, and sometimes sudden death, typically triggered by exertion.

  • Echocardiography is done, but, if available, MRI best shows the abnormal myocardium.

  • Use beta-blockers and/or rate-limiting calcium channel blockers (usually verapamil) to decrease myocardial contractility and slow the heart rate and thus prolong diastolic filling and decrease outflow obstruction.

  • Consider mavacamten to decrease left ventricular outflow tract gradient, improve exercise capacity, and reduce symptoms.

  • Avoid nitrates and other drugs that decrease preload (eg, diuretics, angiotensin-converting enzyme inhibitors, angiotensin II receptor blockers) because these decrease left ventricular size and worsen left ventricular function.

  • Place an implantable cardioverter-defibrillator for patients with syncope or sudden cardiac arrest.

  • Do surgical myectomy or alcohol septal ablation in patients with symptoms despite medical therapy.

More Information

The following English-language resource may be useful. Please note that THE MANUAL is not responsible for the content of this resource.

  • American Heart Association Guidelines on Hypertrophic Cardiomyopathy: Ommen SR, Mital S, Burke MA, et al: 2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation 20 November 2020. doi: 10.1161/CIR.0000000000000937

Drugs Mentioned In This Article

Drug Name Select Trade
Calan, Calan SR, Covera-HS, Isoptin, Isoptin SR, Verelan, Verelan PM
Norpace, Norpace CR
Deponit, GONITRO , Minitran, Nitrek, Nitro Bid, Nitrodisc, Nitro-Dur, Nitrogard , Nitrol, Nitrolingual, NitroMist , Nitronal, Nitroquick, Nitrostat, Nitrotab, Nitro-Time, RECTIV, Transdermal-NTG, Tridil
Cordarone, Nexterone, Pacerone
Cardizem, Cardizem CD, Cardizem LA, Cardizem SR, Cartia XT , Dilacor XR, Dilt-CD , Diltia XT, Diltzac, Matzim LA, Taztia XT, TIADYLT ER, Tiamate, Tiazac
NOTE: This is the Professional Version. CONSUMERS: View Consumer Version
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