Low frequency of detection by nested polymerase chain reaction of enterovirus ribonucleic acid in endomyocardial tissue of patients with idiopathic dilated cardiomyopathy
M Giacca,
GM Severini,
L Mestroni,
A Salvi,
G Lardieri,
A Falaschi,
and
F Camerini
International Centre for Genetic Engineering and Biotechnology (UNIDO), Trieste, Italy.
OBJECTIVES. The purpose of this study was to determine the prevalence of enteroviral infection in the myocardium of patients with idiopathic dilated cardiomyopathy by using a highly sensitive and specific detection technique. BACKGROUND. Recent molecular studies have suggested that enteroviral persistence (in particular, coxsackieviruses type B) may underlie idiopathic myocarditis and dilated cardiomyopathy. METHODS. The method used to detect enterovirus-specific ribonucleic acids (RNAs) is based on reverse transcription and nested polymerase chain reaction amplification with four pairs of primers from the conserved 5' noncoding region of the enteroviral genome. Several members of the Enterovirus genus are detectable by this assay (coxsackieviruses B1 to B6; polioviruses 1 to 3; echoviruses 9, 19 and 31), with a sensitivity threshold close to the detection of a single molecule of viral RNA in 1 mg of tissue sample. Endomyocardial tissue samples from 84 subjects were analyzed (77 samples obtained from left endomyocardial biopsies, 7 from explanted hearts). The subjects comprised 63 study patients (53 with dilated cardiomyopathy, 3 with idiopathic myocarditis, 1 with right ventricular dysplasia, 1 with restrictive cardiomyopathy, 1 with eosinophilic myocarditis, 1 with primary ventricular fibrillation and 3 with myocarditis of known etiology) and 21 control subjects with other diseases. RESULTS. Positive signals were obtained only in samples from six study patients (four with dilated cardiomyopathy, one with right ventricular dysplasia and one with myocarditis). Samples from control subjects, uninfected rat myocardium and cultured cell lines yielded systematically negative results. Moreover, the nucleotide sequence analysis of the amplification products from patients with positive samples raised doubts about the true positivity of these samples. CONCLUSIONS. This study suggests that the persistence of enteroviral RNA in dilated cardiomyopathy is not a major cause of the disease and that a careful analysis of polymerase chain reaction amplification products is essential in any study in which this technique is pushed to high sensitivity thresholds.
This article has been cited by other articles:

|
 |

|
 |
 
F. Calabrese and G. Thiene
Myocarditis and inflammatory cardiomyopathy: microbiological and molecular biological aspects
Cardiovasc Res,
October 15, 2003;
60(1):
11 - 25.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Frustaci, F. Calabrese, C. Chimenti, M. Pieroni, G. Thiene, and A. Maseri
Lone Hepatitis C Virus Myocarditis Responsive to Immunosuppressive Therapy
Chest,
October 1, 2002;
122(4):
1348 - 1356.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
N G Mahon, B Zal, G Arno, P Risley, J Pinto-Basto, W J McKenna, M J Davies, and C Baboonian
Absence of viral nucleic acids in early and late dilated cardiomyopathy
Heart,
December 1, 2001;
86(6):
687 - 692.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. P. Liu and J. W. Mason
Advances in the Understanding of Myocarditis
Circulation,
August 28, 2001;
104(9):
1076 - 1082.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A D'Ambrosio, G Patti, A Manzoli, G Sinagra, A Di Lenarda, F Silvestri, and G Di Sciascio
The fate of acute myocarditis between spontaneous improvement and evolution to dilated cardiomyopathy: a review
Heart,
May 1, 2001;
85(5):
499 - 504.
[Full Text]
|
 |
|

|
 |

|
 |
 
C. Basso, F. Calabrese, D. Corrado, and G. Thiene
Postmortem diagnosis in sudden cardiac death victims: macroscopic, microscopic and molecular findings
Cardiovasc Res,
May 1, 2001;
50(2):
290 - 300.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. Fujioka, Y. Kitaura, A. Ukimura, H. Deguchi, K. Kawamura, T. Isomura, H. Suma, and A. Shimizu
Evaluation of viral infection in the myocardium of patients with idiopathic dilated cardiomyopathy
J. Am. Coll. Cardiol.,
November 15, 2000;
36(6):
1920 - 1926.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. Calabrese, A. Angelini, G. Thiene, C. Basso, A. Nava, and M. Valente
No detection of enteroviral genome in the myocardium of patients with arrhythmogenic right ventricular cardiomyopathy
J. Clin. Pathol.,
May 1, 2000;
53(5):
382 - 387.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Kawai
From Myocarditis to Cardiomyopathy: Mechanisms of Inflammation and Cell Death : Learning From the Past for the Future
Circulation,
March 2, 1999;
99(8):
1091 - 1100.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G N Dalekos, K Achenbach, D Christodoulou, G K Liapi, E K Zervou, D A Sideris, and E V Tsianos
Idiopathic dilated cardiomyopathy: lack of association with hepatitis C virus infection
Heart,
September 1, 1998;
80(3):
270 - 275.
[Abstract]
[Full Text]
|
 |
|

|
 |

|
 |
 
A. P. Burke, A. Farb, G. Tashko, and R. Virmani
Arrhythmogenic Right Ventricular Cardiomyopathy and Fatty Replacement of the Right Ventricular Myocardium : Are They Different Diseases?
Circulation,
April 28, 1998;
97(16):
1571 - 1580.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Baboonian and T. Treasure
Meta-analysis of the association of enteroviruses with human heart disease
Heart,
December 1, 1997;
78(6):
539 - 543.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Okabe, K. Fukuda, K. Arakawa, and M. Kikuchi
Chronic Variant of Myocarditis Associated With Hepatitis C Virus Infection
Circulation,
July 1, 1997;
96(1):
22 - 24.
[Abstract]
[Full Text]
|
 |
|

|
 |

|
 |
 
A. Matsumori, Y. Matoba, and S. Sasayama
Dilated Cardiomyopathy Associated With Hepatitis C Virus Infection
Circulation,
November 1, 1995;
92(9):
2519 - 2525.
[Abstract]
[Full Text]
|
 |
|
|