|Other names||Congestive cardiomyopathy,|
|Mouse heart slice showing dilated cardiomyopathy|
|Symptoms||Feeling tired, leg swelling, shortness of breath, chest pain, fainting|
|Complications||Heart failure, heart valve disease, irregular heartbeat|
|Usual onset||Middle age|
|Causes||Genetics, alcohol, cocaine, certain toxins, complications of pregnancy, certain infections|
|Diagnostic method||Supported by electrocardiogram, chest X-ray, echocardiogram|
|Differential diagnosis||Coronary artery disease, heart valve disease, pulmonary embolism, other cardiomyopathy|
|Treatment||Lifestyle changes, medications, implantable cardioverter defibrillator, heart transplant|
|Medication||ACE inhibitor, beta blocker, diuretic, blood thinners|
|Prognosis||Five-year survival rate ~50%|
|Frequency||1 in 2,500|
Dilated cardiomyopathy (DCM) is a condition in which the heart becomes enlarged and cannot pump blood effectively. Symptoms vary from none to feeling tired, leg swelling, and shortness of breath. It may also result in chest pain or fainting. Complications can include heart failure, heart valve disease, or an irregular heartbeat.
Causes include genetics, alcohol, cocaine, certain toxins, complications of pregnancy, and certain infections. Coronary artery disease and high blood pressure may play a role, but are not the primary cause. In many cases the cause remains unclear. It is a type of cardiomyopathy, a group of diseases that primarily affects the heart muscle. The diagnosis may be supported by an electrocardiogram, chest X-ray, or echocardiogram.
In those with heart failure, treatment may include medications in the ACE inhibitor, beta blocker, and diuretic families. A low salt diet may also be helpful. In those with certain types of irregular heartbeat, blood thinners or an implantable cardioverter defibrillator may be recommended. If other measures are not effective a heart transplant may be an option in some.
About 1 per 2,500 people are affected. It occurs more frequently in men than women. Onset is most often in middle age. Five-year survival rate is about 50%. It can also occur in children and is the most common type of cardiomyopathy in this age group.
- 1 Signs and symptoms
- 2 Causes
- 3 Pathophysiology
- 4 Diagnosis
- 5 Treatment
- 6 Epidemiology
- 7 Research directions
- 8 Other animals
- 9 References
- 10 External links
Signs and symptoms
Dilated cardiomyopathy develops insidiously, and may not initially cause symptoms significant enough to impact on quality of life. Nevertheless, many people experience significant symptoms. These might include:
A person suffering from dilated cardiomyopathy may have an enlarged heart, with pulmonary edema and an elevated jugular venous pressure and a low pulse pressure. Signs of mitral and tricuspid regurgitation may be present.
Although in many cases no cause is apparent, dilated cardiomyopathy is probably the result of damage to the myocardium produced by a variety of toxic, metabolic, or infectious agents. It may be due to fibrous change of the myocardium from a previous myocardial infarction. Or, it may be the late sequelae of acute viral myocarditis, such as with Coxsackie B virus and other enteroviruses possibly mediated through an immunologic mechanism.
Other causes include:
- Chagas disease, due to Trypanosoma cruzi. This is the most common infectious cause of dilated cardiomyopathy in Latin America
- Pregnancy. Dilated cardiomyopathy occurs late in gestation or several weeks to months postpartum as a peripartum cardiomyopathy. It is reversible in half of cases.
- Alcohol abuse (alcoholic cardiomyopathy)
- Nonalcoholic toxic insults include administration of certain chemotherapeutic agents, in particular doxorubicin (Adriamycin), and cobalt.
- Thyroid disease
- Inflammatory diseases such as sarcoidosis and connective tissue diseases
- Tachycardia-induced cardiomyopathy
- Muscular dystrophy
- Tuberculosis - 1 to 2% of TB cases.
- Autoimmune mechanisms
- Thiamine deficiency
Recent studies have shown that those subjects with an extremely high occurrence (several thousands a day) of premature ventricular contractions (extrasystole) can develop dilated cardiomyopathy. In these cases, if the extrasystole are reduced or removed (for example, via ablation therapy) the cardiomyopathy usually regresses.
|Genetic associations with dilated cardiomyopathy|
|CMD1B||unknown (TMOD1 candidate)||9q13|
About 25–35% of affected individuals have familial forms of the disease, with most mutations affecting genes encoding cytoskeletal proteins, while some affect other proteins involved in contraction. The disease is genetically heterogeneous, but the most common form of its transmission is an autosomal dominant pattern. Autosomal recessive (as found, for example, in Alström syndrome), X-linked (as in Duchenne muscular dystrophy), and mitochondrial inheritance of the disease is also found. Some relatives of those affected by dilated cardiomyopathy have preclinical, asymptomatic heart-muscle changes.
Other cytoskeletal proteins involved in DCM include α-cardiac actin, desmin, and the nuclear lamins A and C. Mitochondrial deletions and mutations presumably cause DCM by altering myocardial ATP generation.
Kayvanpour et al. performed 2016 a meta-analysis with the largest dataset available on genotype-phenotype associations in DCM and mutations in lamin (LMNA), phospholamban (PLN), RNA Binding Motif Protein 20 (RBM20), Cardiac Myosin Binding Protein C (MYBPC3), Myosin Heavy Chain 7 (MYH7), Cardiac Troponin T 2 (TNNT2), and Cardiac Troponin I (TNNI3). They also reviewed recent studies investigating genotype-phenotype associations in DCM patients with titin (TTN) mutations. LMNA and PLN mutation carriers showed a high prevalence of cardiac transplantation and ventricular arrhythmia. Dysrhythmias and sudden cardiac death (SCD) was shown to occur even before the manifestation of DCM and heart failure symptoms in LMNA mutation carriers.
The progression of heart failure is associated with left ventricular remodeling, which manifests as gradual increases in left ventricular end-diastolic and end-systolic volumes, wall thinning, and a change in chamber geometry to a more spherical, less elongated shape. This process is usually associated with a continuous decline in ejection fraction. The concept of cardiac remodeling was initially developed to describe changes that occur in the days and months following myocardial infarction.
As DCM progresses, two compensatory mechanisms are activated in response to impaired myocyte contractility and reduced stroke volume:
- Frank-Starling law
- Neurohormonal feedback, via activation of the sympathetic nervous system and the renin-angiotensin system.
These responses initially compensate for decreased cardiac output and maintain those with DCM as asymptomatic. Eventually, however, these mechanisms become detrimental, intravascular volume becomes too great, and progressive dilatation leads to heart failure symptoms.
Cardiac dilatation is a transversely isotropic, irreversible process resulting from excess strains on the myocardium. A computation model of volumetric, isotropic, and cardiac wall growth predicts the relationship between cardiac strains (e.g. volume overload after myocardial infarction) and dilation using the following governing equations:
where is elastic volume stretch that is reversible and is irreversible, isotropic volume growth described by:
where is a vector, which points along a cardiomyocyte's long axis and is the cardiomyocyte stretch due to growth. The total cardiomyocyte growth is given by:
The above model reveals a gradual dilation of the myocardium, especially the ventricular myocardium, to support the blood volume overload in the chambers. Dilation manifests itself in an increase in total cardiac mass and cardiac diameter. Cardiomyocytes reach their maximum length of 150 m in the endocardium and 130 m in the epicardium by the addition of sarcomeres. Due to the increase in diameter, the dilated heart appears spherical in shape, as opposed the elliptical shape of a healthy human heart. In addition, the ventricular walls maintain the same thickness, characteristic of pathophysiological cardiac dilation.
As the ventricles enlarge, both the mitral and tricuspid valves may lose their ability to come together properly. This loss of coaptation may lead to mitral and tricuspid regurgitation. As a result, those with DCM are at increased risk of atrial fibrillation. Furthermore, stroke volume is decreased and a greater volume load is placed on the ventricle, thus increasing heart failure symptoms.
The electrocardiogram often shows sinus tachycardia or atrial fibrillation, ventricular arrhythmias, left atrial enlargement, and sometimes intraventricular conduction defects and low voltage. When left bundle-branch block (LBBB) is accompanied by right axis deviation (RAD), the rare combination is considered to be highly suggestive of dilated or congestive cardiomyopathy. Echocardiogram shows left ventricular dilatation with normal or thinned walls and reduced ejection fraction. Cardiac catheterization and coronary angiography are often performed to exclude ischemic heart disease.
Genetic testing can be important, since one study has shown that gene mutations in the TTN gene (which codes for a protein called titin) are responsible for "approximately 25% of familial cases of idiopathic dilated cardiomyopathy and 18% of sporadic cases." The results of the genetic testing can help the doctors and patients understand the underlying cause of the dilated cardiomyopathy. Genetic test results can also help guide decisions on whether a patient's relatives should undergo genetic testing (to see if they have the same genetic mutation) and cardiac testing to screen for early findings of dilated cardiomyopathy.
Drug therapy can slow down progression and in some cases even improve the heart condition. Standard therapy may include salt restriction, ACE inhibitors, diuretics, and beta blockers. Anticoagulants may also be used for antithrombotic therapy. There is some evidence for the benefits of coenzyme Q10 in treating heart failure.
Artificial pacemakers may be used in patients with intraventricular conduction delay, and implantable cardioverter-defibrillators in those at risk of arrhythmia. These forms of treatment have been shown to prevent sudden cardiac death, improve symptoms, and reduce hospitalization in patients with systolic heart failure.
In patients with advanced disease who are refractory to medical therapy, heart transplantation may be considered. For these people 1-year survival approaches 90% and over 50% survive greater than 20 years.
Although the disease is more common in African-Americans than in Caucasians, it may occur in any patient population.
Dilated cardiomyopathy is a heritable disease in some dog breeds, including the Boxer, Dobermann, Great Dane, Irish Wolfhound, and St Bernard. Treatment is based on medication, including ACE inhibitors, loop diuretics, and phosphodiesterase inhibitors.
Dilated cardiomyopathy is also a disease affecting some cat breeds, including the Oriental Shorthair, Burmese, Persian, and Abyssinian. In cats, taurine deficiency is the most common cause of dilated cardiomyopathy. As opposed to these hereditary forms, non-hereditary DCM used to be common in the overall cat population before the addition of taurine to commercial cat food.
There is also a high incidence of heritable dilated cardiomyopathy in captive Golden Hamsters (Mesocricetus auratus), due in no small part to their being highly inbred. The incidence is high enough that several strains of Golden Hamster have been developed to serve as animal models in clinical testing for human forms of the disease.
- "Other Names for Cardiomyopathy". NHLBI. June 22, 2016. Retrieved 31 August 2016.
- "What Are the Signs and Symptoms of Cardiomyopathy?". NHLBI. 22 June 2016. Retrieved 10 November 2017.
- "What Is Cardiomyopathy?". NHLBI. 22 June 2016. Retrieved 10 November 2017.
- "Types of Cardiomyopathy". NHLBI. 22 June 2016. Retrieved 10 November 2017.
- Ferri, Fred F. (2017). Ferri's Clinical Advisor 2018 E-Book: 5 Books in 1. Elsevier Health Sciences. p. 244. ISBN 9780323529570.
- "Tachycardia-induced cardiomyopathy". European Society of Cardiology. 2019-03-29. Retrieved 2019-03-29.
Tachycardia-induced cardiomyopathy is a reversible cause of heart failure and dilated cardiomyopathy. Tachycardia-induced cardiomyopathy should be considered in all patients with a dilated cardiomyopathy of uncertain origin and who have tachycardia or atrial fibrillation with a fast ventricular rate.
- Umana, Ernesto; Solares, C. Arturo; Alpert, Martin A (2003-01-01). "Tachycardia-induced cardiomyopathy". The American Journal of Medicine. 114 (1): 51–55. doi:10.1016/S0002-9343(02)01472-9.
- "What Causes Cardiomyopathy?". NHLBI. 22 June 2016. Retrieved 10 November 2017.
- Weintraub, RG; Semsarian, C; Macdonald, P (22 July 2017). "Dilated cardiomyopathy". Lancet. 390 (10092): 400–414. doi:10.1016/S0140-6736(16)31713-5. PMID 28190577.
- "Who Is at Risk for Cardiomyopathy? - NHLBI, NIH". NHLBI. 22 June 2016. Retrieved 10 November 2017.
- Watkins, Hugh; Ashrafian, Houman; Redwood, Charles (2011-04-27). "Inherited Cardiomyopathies". New England Journal of Medicine. 364 (17): 1643–1656. doi:10.1056/nejmra0902923. PMID 21524215.
- Pathophysiology of heart disease : a collaborative project of medical students and faculty. Lilly, Leonard S., Harvard Medical School. (5th ed.). Baltimore, MD: Wolters Kluwer/Lippincott Williams & Wilkins. 2011. ISBN 9781605477237. OCLC 649701807.CS1 maint: others (link)
- Mitchell, Richard Sheppard; Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson (2007). Robbins Basic Pathology (8th ed.). Philadelphia: Saunders. ISBN 978-1-4160-2973-1.
- Martino TA, Liu P, Sole MJ (February 1994). "Viral infection and the pathogenesis of dilated cardiomyopathy". Circ. Res. 74 (2): 182–8. doi:10.1161/01.res.74.2.182. PMID 8293557.
- "Dilated Cardiomyopathy - Cardiovascular Disorders".
- Ritesh Agarwal, corresponding author Puneet Malhotra, Anshu Awasthi, Nandita Kakkar, and Dheeraj Gupta. Tuberculous dilated cardiomyopathy: an under-recognized entity?" BMC Infect Dis 2005; 5: 29. Published online 2005 Apr 27. doi:10.1186/1471-2334-5-29
- San Martín MA, García A, Rodríguez FJ, Terol I (May 2002). "[Dilated cardiomyopathy and autoimmunity: an overview of current knowledge and perspectives]". Rev Esp Cardiol. (in Spanish). 55 (5): 514–24. doi:10.1016/s0300-8932(02)76644-x. PMID 12015932. Archived from the original on 2009-01-09.
- Belhassen B (April 2005). "Radiofrequency ablation of "benign" right ventricular outflow tract extrasystoles: a therapy that has found its disease?". J. Am. Coll. Cardiol. 45 (8): 1266–8. doi:10.1016/j.jacc.2005.01.028. PMID 15837260.
- Shiraishi H, Ishibashi K, Urao N, et al. (November 2002). "A case of cardiomyopathy induced by premature ventricular complexes". Circ. J. 66 (11): 1065–7. doi:10.1253/circj.66.1065. PMID 12419942.
- Ross J (March 2002). "Dilated cardiomyopathy: concepts derived from gene deficient and transgenic animal models". Circ. J. 66 (3): 219–24. doi:10.1253/circj.66.219. PMID 11922267.
- Schönberger J, Seidman CE (August 2001). "Many roads lead to a broken heart: the genetics of dilated cardiomyopathy". American Journal of Human Genetics. 69 (2): 249–60. doi:10.1086/321978. PMC 1235300. PMID 11443548.
- Mahon NG, Murphy RT, MacRae CA, Caforio AL, Elliott PM, McKenna WJ (July 2005). "Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease". Annals of Internal Medicine. 143 (2): 108–15. doi:10.7326/0003-4819-143-2-200507190-00009. PMID 16027452.
- Kayvanpour, Elham; Sedaghat-Hamedani, Farbod; Amr, Ali; Lai, Alan; Haas, Jaan; Holzer, Daniel B.; Frese, Karen S.; Keller, Andreas; Jensen, Katrin; Katus, Hugo A.; Meder, Benjamin (2016-08-30). "Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals". Clinical Research in Cardiology. 106 (2): 127–139. doi:10.1007/s00392-016-1033-6. PMID 27576561.
- Pieske B (2004). "Reverse remodeling in heart failure – fact or fiction?". Eur Heart J Suppl. 6: D66–78. doi:10.1016/j.ehjsup.2004.05.019.
- Goektepe, Serdar; Abilez, Oscar John; Kuhl, Ellen (2010). "Generic approach towards finite growth with examples of athlete's heart, cardiac dilation, and cardiac wall thickening". Mechanics and Physics of Solids. 58 (10): 1661–1680. doi:10.1016/j.jmps.2010.07.003.
- Goektepe, Serdar; Abilez, Oscar John; Parker, K; Kuhl, Ellen (2010). "A multiscale model for eccentric and concentric cardiac growth through sarcomerogenesis". Theoretical Biology. 58: 1661–1680. doi:10.1016/j.jmps.2010.07.003.
- Nikolic G, Marriott HJ (Oct 1985). "Left bundle branch block with right axis deviation: a marker of congestive cardiomyopathy". J Electrocardiol. 18 (4): 395–404. doi:10.1016/s0022-0736(85)80022-4. PMID 3906012.
- Childers R, Lupovich S, Sochanski M, Konarzewska H (2000). "Left bundle branch block and right axis deviation: a report of 36 cases". J Electrocardiol. 33 (Suppl): 93–102. doi:10.1054/jclc.2000.20326. PMID 11265743.
- Herman DS, Lam L, Taylor MR, Wang L, Teekakirikul P, Christodoulou D, Conner L, DePalma SR, McDonough B, Sparks E, Teodorescu DL, Cirino AL, Banner NR, Pennell DJ, Graw S, Merlo M, Di Lenarda A, Sinagra G, Bos JM, Ackerman MJ, Mitchell RN, Murry CE, Lakdawala NK, Ho CY, Barton PJ, Cook SA, Mestroni L, Seidman JG, Seidman CE (Feb 16, 2012). "Truncations of Titin causing dilated cardiomyopathy". N Engl J Med. 366 (7): 619–628. doi:10.1056/NEJMoa1110186. PMC 3660031. PMID 22335739.
- Pennell DJ, Sechtem UP, Higgins CB, Manning WJ, Pohost GM, Rademakers FE, van Rossum AC, Shaw LJ, Yucel EK (Nov 2004). "Clinical indications for cardiovascular magnetic resonance (CMR): Consensus Panel report". Eur Heart J. 25 (21): 1940–1965. doi:10.1016/j.ehj.2004.06.040. PMID 15522474.
- Langsjoen PH, Langsjoen PH, Folkers K (1990). "A six-year clinical study of therapy of cardiomyopathy with coenzyme Q10". Int J Tissue React. 12 (3): 169–71. PMID 2276895.
- Folkers K, Langsjoen P, Langsjoen PH (January 1992). "Therapy with coenzyme Q10 of patients in heart failure who are eligible or ineligible for a transplant". Biochem Biophys Res Commun. 182 (1): 247–53. doi:10.1016/S0006-291X(05)80137-8. PMID 1731784.
- Baggio E, Gandini R, Plancher AC, Passeri M, Carmosino G (1994). "Italian multicenter study on the safety and efficacy of coenzyme Q10 as adjunctive therapy in heart failure. CoQ10 Drug Surveillance Investigators". Mol. Aspects Med. 15 (Suppl): s287–94. doi:10.1016/0098-2997(94)90040-X. PMID 7752841.
- McPhee, Stephen J.; Rabow, Michael W.; Papadakis, Maxine A. (2016-09-01). Current medical diagnosis & treatment 2017. Papadakis, Maxine A.,, McPhee, Stephen J.,, Rabow, Michael W. (Fifty-sixth ed.). New York. ISBN 978-1259585111. OCLC 957316517.
- Coughlin SS, Labenberg JR, Tefft MC (March 1993). "Black-white differences in idiopathic dilated cardiomyopathy: the Washington DC dilated Cardiomyopathy Study". Epidemiology. 4 (2): 165–72. doi:10.1097/00001648-199303000-00013. PMID 8452906.
- Reis Filho JR, Cardoso JN, Cardoso CM, Pereira-Barretto AC (2015). "Reverse Cardiac Remodeling: A Marker of Better Prognosis in Heart Failure". Arq. Bras. Cardiol. 104 (6): 502–6. doi:10.5935/abc.20150025. PMC 4484683. PMID 26131706.
- Oyama MA, Chittur S (July 2005). "Genomic expression patterns of cardiac tissues from dogs with dilated cardiomyopathy". Am J Vet Res. 66 (7): 1140–55. doi:10.2460/ajvr.2005.66.1140. PMID 16111151.
- Pion, P. D.; Kittleson, M. D.; Thomas, W. P.; Skiles, M. L.; Rogers, Q. R. (1992-07-15). "Clinical findings in cats with dilated cardiomyopathy and relationship of findings to taurine deficiency". Journal of the American Veterinary Medical Association. 201 (2): 267–274. ISSN 0003-1488. PMID 1500323.
- Nigro V, Okazaki Y, Belsito A, et al. (April 1997). "Identification of the Syrian hamster cardiomyopathy gene". Hum. Mol. Genet. 6 (4): 601–7. doi:10.1093/hmg/6.4.601. PMID 9097966.
- Dilated cardiomyopathy information for parents.