Usefulness of DNA quantification in diagnosis of hypertrophic cardiomyopathies: A preliminary study

作者: F. Martínez Díaz , M. Bernal Gilar , A. Ruiz Saurí , A. Llombart Bosh , A. Luna

DOI: 10.1016/J.FORSCIINT.2005.02.035

关键词: Heart diseaseHypertrophic cardiomyopathyDifferential diagnosisMuscle hypertrophyVentricleSudden deathPathologyCardiomyopathyPathogenesisMedicine

摘要: Hypertrophic cardiomyopathies (HCM) are a frequent cause of sudden death in both young people and adults. Different can be distinguished according to the etiological agent and, although there morphological differences too, alterations quantity DNA cardiomyocytes may play an important role their pathogenesis evolution. To understand characteristics behaviour index hypertrophic cardiomyopathies, we have studied thirty cases (10 primaries or essential, 10 hypertensives toxic) compared results with those obtained for macroscopically normal hearts. The showed that different were statistically related age, heart weight ventricle thickness. hearts showing diploid index, hypertensive (CM) tetraploid toxic CM (1.1-1.9) essential (>2) aneuploid index. Statistically significant associations (p < 0.001) observed when values type CM, thickness ventricles weight. Therefore, think technique described great help differential diagnosis cardiomyopathies.

参考文章(20)
Alfonso F, Cardiomyopathies. VIII. Sudden death in hypertrophic cardiomyopathy Revista Espanola De Cardiologia. ,vol. 49, pp. 288- 304 ,(1996)
Claus-Peter Adler, Michael Neuburger, Georg W. Herget, Dietmar M�hlbach, Regeneration processes in human myocardium after acute ischaemia--quantitative determination of DNA, cell number and collagen content. Virchows Archiv. ,vol. 430, pp. 149- 153 ,(1997) , 10.1007/BF01008036
Atsushi Takeda, Nobuakira Takeda, Different Pathophysiology of Cardiac Hypertrophy in Hypertension and Hypertrophic Cardiomyopathy Journal of Molecular and Cellular Cardiology. ,vol. 29, pp. 2961- 2965 ,(1997) , 10.1006/JMCC.1997.0531
A. Arola, E. Jokinen, O. Ruuskanen, M. Saraste, E. Pesonen, A.-L. Kuusela, T. Tikanoja, T. Paavilainen, O. Simell, Epidemiology of Idiopathic Cardiomyopathies in Children and Adolescents A Nationwide Study in Finland American Journal of Epidemiology. ,vol. 146, pp. 385- 393 ,(1997) , 10.1093/OXFORDJOURNALS.AJE.A009291
Josep Brugada, Muerte súbita en la miocardiopatía hipertrófica Revista Española de Cardiología. ,vol. 51, pp. 991- 996 ,(1998) , 10.1016/S0300-8932(98)74853-5
Jamshid Shirani, Ruth Pick, William C Roberts, Barry J Maron, Morphology and significance of the left ventricular collagen network in young patients with hypertrophic cardiomyopathy and sudden cardiac death Journal of the American College of Cardiology. ,vol. 35, pp. 36- 44 ,(2000) , 10.1016/S0735-1097(99)00492-1
Nasser M. Lakkis, Sherif F. Nagueh, Neal S. Kleiman, Donna Killip, Zuo-Xiang He, Mario S. Verani, Robert Roberts, William H. Spencer, Echocardiography-Guided Ethanol Septal Reduction for Hypertrophic Obstructive Cardiomyopathy Circulation. ,vol. 98, pp. 1750- 1755 ,(1998) , 10.1161/01.CIR.98.17.1750
V. Ya. Brodsky, A. L. Chernyaev, I. A. Vasilyeva, Variability of the cardiomyocyte ploidy in normal human hearts Virchows Archiv B Cell Pathology Including Molecular Pathology. ,vol. 61, pp. 289- 294 ,(1992) , 10.1007/BF02890430
M.J. DAVIES, W.J. McKENNA, Hypertrophic cardiomyopathy — pathology and pathogenesis Histopathology. ,vol. 26, pp. 493- 500 ,(1995) , 10.1111/J.1365-2559.1995.TB00267.X