Causes
By Mayo Clinic staffYour heart beats about 100,000 times a day to circulate blood throughout your body. To pump blood, your heart's chambers contract and relax. These actions are controlled by electrical impulses created in the sinus node, a group of cells in the upper right chamber of your heart. These impulses travel through your heart and cause it to beat.
After each heartbeat, your heart's electrical system recharges itself in preparation for the next heartbeat. This process is known as repolarization. In long QT syndrome, your heart muscle takes longer than normal to recharge between beats. This electrical disturbance, which often can be seen on an electrocardiogram (ECG), is called a prolonged Q-T interval.
Prolonged Q-T interval
An electrocardiogram (ECG, also called an EKG) measures electrical impulses as they travel through your heart. Patches with wires attached to your skin measure these impulses, which are displayed on a monitor or printed on paper as waves of electrical activity.
An ECG measures electrical impulses as five distinct waves. Doctors label these five waves using the letters P, Q, R, S and T. The waves labeled Q through T show electrical activity in your heart's lower chambers.
The space between the start of the Q wave and the end of the T wave (Q-T interval) corresponds to the time it takes for your heart to contract and then refill with blood before beginning the next contraction.
By measuring the Q-T interval, doctors can tell whether it occurs in a normal amount of time. If it takes longer than normal, it's called a prolonged Q-T interval. The upper limit of a normal Q-T interval takes into account age, sex, and regularity and speed of the heart rate.
Long QT syndrome results from abnormalities in the heart's electrical recharging system. However, the heart's structure is normal. Abnormalities in your heart's electrical system may be inherited or acquired due to an underlying medical condition or a medication.
Inherited long QT syndrome
At least 12 genes associated with long QT syndrome have been discovered so far, and hundreds of mutations within these genes have been identified. Mutations in three of these genes account for about 70 to 75 percent of long QT syndrome, and cause the forms referred to as LQT1, LQT2 and LQT3.
Doctors have described two forms of inherited long QT syndrome:
- Romano-Ward syndrome. This more common form occurs in people who inherit only a single genetic variant from one of their parents.
- Jervell and Lange-Nielsen syndrome. Signs and symptoms of this rare form usually occur earlier and are more severe than in Romano-Ward syndrome. It's seen in children who are born deaf and have long QT syndrome because they inherited genetic variants from each parent.
Additionally, scientists have been investigating a possible link between SIDS and long QT syndrome and have discovered that about 10 percent of babies with SIDS had a genetic defect or mutation for long QT syndrome.
Acquired long QT syndrome
More than 50 medications, many of them common, can lengthen the Q-T interval in otherwise healthy people and cause a form of acquired long QT syndrome known as drug-induced long QT syndrome.
Medications that can lengthen the Q-T interval and upset heart rhythm include certain antibiotics, antidepressants, antihistamines, diuretics, heart medications, cholesterol-lowering drugs, diabetes medications, as well as some antifungal and antipsychotic drugs.
People who develop drug-induced long QT syndrome may also have some subtle genetic defects in their hearts, making them more susceptible to disruptions in heart rhythm from taking drugs that can cause prolonged Q-T intervals.
- Ackerman MJ, et al. Congenital long QT syndrome. In: Gussak I, et al. Electrical Diseases of the Heart; Genetics, Mechanisms, Treatment, Prevention. New York, NY.: Springer; 2008:462.
- Priori SG. Genetics of cardiac arrhythmias. In: Libby P, et al, eds. Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine. 8th ed. Philadelphia, Pa.: Saunders Elsevier; 2007. http://www.mdconsult.com/book/player/book.do?method=display&type=bookPage&decorator=header&eid=4-u1.0-B978-1-4160-4106-1..50012-1--cesec6&uniq=174957165&isbn=978-1-4160-4106-1&sid=927975209#lpState=open&lpTab=contentsTab&content=4-u1.0-B978-1-4160-4106-1..50012-1--cesec1%3Bfrom%3Dtoc%3Btype%3DbookPage%3Bisbn%3D978-1-4160-4106-1. Accessed Dec. 10, 2009.
- Spazzolini C, et al. Clinical implications for patients with long QT syndrome who experience a cardiac event during infancy. Journal of the American College of Cardiology. 2009;54:832.
- Goldenberg I, et al. Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome. Circulation. 2008;117:2184.
- Hobbs JB, et al. Risk of aborted cardiac arrest of sudden cardiac death during adolescence in the long QT syndrome. Journal of the American Medical Association. 2006;296:1249.
- Sauer AJ, et al. Long QT syndrome in adults. Journal of the American College of Cardiology. 2007;49:329.
- Goldenberg I, et al. Long-QT syndrome after age 40. Circulation. 2008;117:2192.
- Johnson JN, et al. Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy. Neurology. 2009;72:224.
- Tester DJ, et al. Cardiomyopathic and channelopathic causes of sudden unexplained death in infants and children. Annual Review of Medicine. 2009;60:69.
- Tester DJ, et al. Effect of clinical phenotype on yield of long QT syndrome genetic testing. Journal of the American College of Cardiology. 2006;47:764.
- Kapa S, et al. Genetic testing for long QT syndrome - Distinguishing pathogenic mutations from benign variants. Circulation. 2009;120:1752.
- Ackerman MJ, et al. Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning. New England Journal of Medicine. 1999;341:1121.
- Tester DJ, et al. Postmortem long QT syndrome genetic testing for sudden unexplained death in the young. Journal of the American College of Cardiology. 2007;49:240.
- Genetic testing: Where to start. The Sudden Arrhythmia Death Syndromes (SADS) Foundation. http://www.sads.org/index.php/General/Where-to-Start.html. Accessed Feb. 6, 2010.
- Taggart NW, et al. Diagnostic miscues in congenital long QT syndrome. Circulation. 2007;115:2613.
- Collura CA, et al. Left cardiac sympathetic denervation for the treatment of long QT syndrome and catecholaminergic polymorphic ventricular tachycardia using video-assisted thoracic surgery. Heart Rhythm. 2009;6:752.
- Zipes DP, et al. Journal of the American College of Cardiology. 2005;45:1354.
- Farnsworth MM, et al. When I go in to wake them ... I Wonder: Parental perceptions about congenital long QT syndrome. Journal of the American Academy of Nurse Practitioners. 2006;18:284.
- Ackerman MJ (expert opinion). Mayo Clinic, Rochester, Minn. Feb. 1, 2010.
- Anand RG, et al. The role of fish oil in arrhythmia prevention. Journal of Cardiopulmonary Rehabilitation and Prevention. 2008;28:92.

Find Mayo Clinic on