Serological and molecular evidence of enterovirus infection in patients with end-stage dilated cardiomyopathy

被引:38
作者
Muir, P
Nicholson, F
Illavia, SJ
McNeil, TS
Ajetunmobi, JF
Dunn, H
Starkey, WG
Reetoo, KN
Cary, NRB
Parameshwar, J
Banatvala, JE
机构
[1] PAPWORTH HOSP,DEPT HISTOPATHOL,CAMBRIDGE,ENGLAND
[2] PAPWORTH HOSP,TRANSPLANT UNIT,CAMBRIDGE,ENGLAND
关键词
cardiomyopathy; enterovirus RNA detection; enterovirus-specific immunoglobulin M responses;
D O I
10.1136/hrt.76.3.243
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective - To study the relative diagnostic value of enterovirus-specific molecular biological and serological assays in patients with end-stage dilated cardiomyopathy, and to investigate the possible role of other cardiotropic viruses in dilated cardiomyopathy. Design - Analysis of recipient myocardial tissue and serum from patients with dilated cardiomyopathy and controls undergoing cardiac transplantation for end-stage cardiac disease. Setting - University virology department and transplantation unit. Methods - Reverse transcriptase-polymerase chain reaction and nucleotide sequence analysis of myocardial RNA and DNA; enterovirus-specific in situ hybridisation; enterovirus-specific immunoglobulin M detection. Results - Enterovirus RNA was detected in myocardial tissue from only a small proportion of (five of 75) hearts. However, although enterovirus-specific immunoglobulin M responses were detected in 22 (28%) of 39 controls patients, a significantly higher prevalence was observed among patients with dilated cardiomyopathy (22 (56%) of 39 patients; P < 0.005). All enteroviruses detected in myocardium showed greatest nucleotide sequence homology with coxsackievirus type B3. Detection of enterovirus RNA in myocardium by the polymerase chain reaction and by in situ hybridisation gave comparable results. Other potentially cardiotropic virus genomes, including human cytomegalovirus, influenzaviruses, and coronaviruses were not detected in myocardium. Conclusion - This study found that enterovirus-specific immunoglobulin M responses provided the strongest evidence of enterovirus involvement in patients with end-stage dilated cardiomyopathy. However, the high background prevalence of these responses limits their diagnostic value. The finding that enteroviruses detected in myocardium were coxsackievirus type B3 accords with recent findings in patients with acute myocarditis, and indicates that this serotype is the major cardiotropic human enterovirus.
引用
收藏
页码:243 / 249
页数:7
相关论文
共 30 条
[1]   AN EXPERIMENTAL-MODEL FOR DILATED CARDIOMYOPATHY AFTER RABBIT CORONAVIRUS INFECTION [J].
ALEXANDER, LK ;
SMALL, JD ;
EDWARDS, S ;
BARIC, RS .
JOURNAL OF INFECTIOUS DISEASES, 1992, 166 (05) :978-985
[2]  
ARCHARD LC, 1988, NEW CONCEPTS VIRAL H, P349
[3]   END-STAGE DILATED CARDIOMYOPATHY - PERSISTENCE OF ENTEROVIRUS RNA IN MYOCARDIUM AT CARDIAC TRANSPLANTATION AND LACK OF IMMUNE-RESPONSE [J].
BOWLES, NE ;
ROSE, ML ;
TAYLOR, P ;
BANNER, NR ;
MORGANCAPNER, P ;
CUNNINGHAM, L ;
ARCHARD, LC ;
YACOUB, MH .
CIRCULATION, 1989, 80 (05) :1128-1136
[4]  
CAMBRIDGE G, 1979, BRIT HEART J, V41, P692
[5]   USE OF THE POLYMERASE CHAIN-REACTION TO ANALYZE SEQUENCE VARIATION WITHIN A MAJOR NEUTRALIZING EPITOPE OF GLYCOPROTEIN-B (GP58) IN CLINICAL ISOLATES OF HUMAN CYTOMEGALOVIRUS [J].
DARLINGTON, J ;
SUPER, M ;
PATEL, K ;
GRUNDY, JE ;
GRIFFITHS, PD ;
EMERY, VC .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :1985-1989
[6]   MYOCARDIAL ENTEROVIRUS INFECTION WITH LEFT-VENTRICULAR DYSFUNCTION - A BENIGN DISEASE COMPARED WITH IDIOPATHIC DILATED CARDIOMYOPATHY [J].
FIGULLA, HR ;
STILLESIEGENER, M ;
MALL, G ;
HEIM, A ;
KREUZER, H .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1995, 25 (05) :1170-1175
[7]  
GRIST NR, 1993, VIRAL INFECTIONS HEA, P23
[8]  
KAMMERER U, 1994, J CLIN MICROBIOL, V32, P285
[9]  
KANDOLF R, 1990, NEW ASPECTS OF POSITIVE-STRAND RNA VIRUSES, P340
[10]   A PROSPECTIVE CASE-CONTROL STUDY OF ANTIBODIES TO COXSACKIE-B VIRUS IN IDIOPATHIC DILATED CARDIOMYOPATHY [J].
KEELING, PJ ;
LUKASZYK, A ;
POLONIECKI, J ;
CAFORIO, ALP ;
DAVIES, MJ ;
BOOTH, JC ;
MCKENNA, WJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1994, 23 (03) :593-598