Diagnosis, prevalence, and screening of familial dilated cardiomyopathy

Bibliography

• Mozaffarian D, Benjamin EJ, Go AS, et al. Heart disease and stroke statistics-2015 update: a report from the american heart association. Circulation 2015;131(4):e29-322
   PubMed Web of Science ®Google Scholar
• Fatkin D. Familial dilated cardiomyopathy: Current challenges and future directions. Global Cardiol Sci Pract 2012;2012(1):8
   Google Scholar
• Fatkin D; Members of the CCGDCWG. Guidelines for the diagnosis and management of familial dilated cardiomyopathy. Heart Lung Circ 2011;20(11):691-3
   Google Scholar
• Maron BJ, Towbin JA, Thiene G, et al. Contemporary definitions and classification of the cardiomyopathies: an american heart association scientific statement from the council on clinical cardiology, heart failure and transplantation committee; quality of care and outcomes research and functional genomics and translational biology interdisciplinary working groups; and council on epidemiology and prevention. Circulation 2006;113(14):1807-16
   PubMed Web of Science ®Google Scholar
• Hershberger RE, Hedges DJ, Morales A. Dilated cardiomyopathy: the complexity of a diverse genetic architecture. Nat Rev Cardiol 2013;10(9):531-47
   PubMed Web of Science ®Google Scholar
• Burkett EL, Hershberger RE. Clinical and genetic issues in familial dilated cardiomyopathy. J Am Col Cardiol 2005;45(7):969-81
   Google Scholar
• Michels VV, Moll PP, Miller FA, et al. The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. N Eng J Med 1992;326(2):77-82
   Google Scholar
• Grunig E, Tasman JA, Kucherer H, et al. Frequency and phenotypes of familial dilated cardiomyopathy. J Am Col Cardiol 1998;31(1):186-94
   PubMedGoogle Scholar
• Mestroni L, Maisch B, McKenna WJ, et al. Guidelines for the study of familial dilated cardiomyopathies. Collaborative research group of the european human and capital mobility project on familial dilated cardiomyopathy. Eur Heart J 1999;20(2):93-102
   PubMedGoogle Scholar
• Hershberger RE, Siegfried JD. Update 2011: clinical and genetic issues in familial dilated cardiomyopathy. J Am Col Cardiol 2011;57(16):1641-9
   PubMedGoogle Scholar
• Sinagra G, Mestroni L, Camerini F. Genetic cardiomyopathies: a clinical approach. Springer; Milan, Italy: 2013
   Google Scholar
• McNally EM, Golbus JR, Puckelwartz MJ. Genetic mutations and mechanisms in dilated cardiomyopathy. J Clin Invest 2013;123(1):19-26
   PubMed Web of Science ®Google Scholar
• Teekakirikul P, Kelly MA, Rehm HL, et al. Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era. J Mol Diagnost 2013;15(2):158-70
   PubMed Web of Science ®Google Scholar
• Karkkainen S, Peuhkurinen K. Genetics of dilated cardiomyopathy. Ann Med 2007;39(2):91-107
   Web of Science ®Google Scholar
• Mestroni L, Tharp CA, Sweet ME, et al. Molecular genetics of dilated cardiomyopathy. eLS 2014
   Google Scholar
• Taylor MR, Carniel E, Mestroni L. Cardiomyopathy, familial dilated. Orpha J Rare Dis 2006;1:27
   Web of Science ®Google Scholar
• Morales A, Cowan J, Dagua J, Hershberger RE. Family history: an essential tool for cardiovascular genetic medicine. Congest Heart Fail 2008;14(1):37-45
   Google Scholar
• Sturm AC, Hershberger RE. Genetic testing in cardiovascular medicine: current landscape and future horizons. Cur Opin Cardiol 2013;28(3):317-25
   Google Scholar
• Mestroni L, Rocco C, Gregori D, et al. Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart muscle disease study group. J Am Col Cardiol 1999;34(1):181-90
   PubMedGoogle Scholar
• Ghosh N, Haddad H. Recent progress in the genetics of cardiomyopathy and its role in the clinical evaluation of patients with cardiomyopathy. Cur Opin Cardiol 2011;26(2):155-64
   Google Scholar
• Monserrat L, Hermida M, Bouzas B, et al. Familial dilated cardiomyopathy in patients transplanted for idiopathic dilated cardiomyopathy. Revi Esp De Cardiol 2002;55(7):725-32
   Google Scholar
• Jacoby D, McKenna WJ. Genetics of inherited cardiomyopathy. Eur Heart J 2012;33(3):296-304
   PubMedGoogle Scholar
• Hershberger RE, Lindenfeld J, Mestroni L, et al. Genetic evaluation of cardiomyopathy–a Heart Failure Society of America practice guideline. J Card Fail 2009;15(2):83-97
   Google Scholar
• Buss SJ, Breuninger K, Lehrke S, et al. Assessment of myocardial deformation with cardiac magnetic resonance strain imaging improves risk stratification in patients with dilated cardiomyopathy. Eur Heart J Cardiova Imag 2015;16(3):307-15
   Google Scholar
• Zecchin M, Di Lenarda A, Gregori D, et al. Are nonsustained ventricular tachycardias predictive of major arrhythmias in patients with dilated cardiomyopathy on optimal medical treatment? Pacing Clin Electrophysiol 2008;31(3):290-9
   PubMedGoogle Scholar
• Fatkin D, Yeoh T, Hayward CS, et al. Evaluation of left ventricular enlargement as a marker of early disease in familial dilated cardiomyopathy. Circ Cardiov Gen 2011;4(4):342-8
   Google Scholar
• Mahon NG, Murphy RT, MacRae CA, et al. Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease. Ann Int Med 2005;143(2):108-15
   PubMedGoogle Scholar
• Moretti M, Merlo M, Barbati G, et al. Prognostic impact of familial screening in dilated cardiomyopathy. Eur J Heart Fail 2010;12(9):922-7
   Google Scholar
• Codd MB, Sugrue DD, Gersh BJ, Melton LJ. 3rd. Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in olmsted county, Minnesota, 1975 – 1984. Circulation 1989;80(3):564-72
   PubMed Web of Science ®Google Scholar
• Maron BJ, Gardin JM, Flack JM, et al. Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults. Circulation 1995;92(4):785-9
   PubMed Web of Science ®Google Scholar
• Manolio TA, Baughman KL, Rodeheffer R, et al. Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute workshop. Am J Cardiol 1992;69(17):1458-66
   Google Scholar
• Miura K, Nakagawa H, Morikawa Y, et al. Epidemiology of idiopathic cardiomyopathy in Japan: results from a nationwide survey. Heart 2002;87(2):126-30
   Google Scholar
• Williams DG, Olsen EG. Prevalence of overt dilated cardiomyopathy in two regions of England. Br Heart J 1985;54(2):153-5
   Google Scholar
• Rakar S, Sinagra G, Di Lenarda A, et al. Epidemiology of dilated cardiomyopathy. A prospective post-mortem study of 5252 necropsies. The heart muscle disease study group. Eur Heart J 1997;18(1):117-23
   Google Scholar
• Petretta M, Pirozzi F, Sasso L, et al. Review and metaanalysis of the frequency of familial dilated cardiomyopathy. Am J Cardiol 2011;108(8):1171-6
   Google Scholar
• Mestroni L, Taylor MR. Genetics and genetic testing of dilated cardiomyopathy: a new perspective. Discov Med 2013;15(80):43-9
   PubMed Web of Science ®Google Scholar
• McNair WP, Sinagra G, Taylor MR, et al. SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism. J Am Col Cardiol 2011;57(21):2160-8
   Google Scholar
• van Rijsingen IA, Arbustini E, Elliott PM, et al. Risk factors for malignant ventricular arrhythmias in lamin a/c mutation carriers a European cohort study. J Am Col Cardiol 2012;59(5):493-500
   PubMed Web of Science ®Google Scholar
• Meune C, Van Berlo JH, Anselme F, et al. Primary prevention of sudden death in patients with lamin A/C gene mutations. N Eng J Med 2006;354(2):209-10
   PubMed Web of Science ®Google Scholar
• Herman DS, Lam L, Taylor MR, et al. Truncations of titin causing dilated cardiomyopathy. N Eng J Med 2012;366(7):619-28
   PubMed Web of Science ®Google Scholar
• Ingles J, Zodgekar PR, Yeates L, et al. Guidelines for genetic testing of inherited cardiac disorders. Heart Lung Circ 2011;20(11):681-7
   PubMed Web of Science ®Google Scholar
• Harakalova M, Kummeling G, Sammani A, et al. A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle-specific genes. Eur J Heart Fail 2015;17(5):484-93
   Google Scholar
• Haas J, Frese KS, Peil B, et al. Atlas of the clinical genetics of human dilated cardiomyopathy. Eur Heart J 2015;36(18):1123-35
   PubMed Web of Science ®Google Scholar