Role of virus-induced myocardial affections in sudden infant death syndrome: A prospective postmortem study

被引:50
作者
Dettmeyer, R
Baasner, A
Schlamann, M
Padosch, SA
Haag, C
Kandolf, R
Madea, B
机构
[1] Univ Bonn, Dept Forens Med, D-53111 Bonn, Germany
[2] Stadt Linikum Solingen, Inst Pathol, D-42653 Solingen, Germany
[3] Univ Tubingen, Inst Pathol, Dept Mol Pathol, D-72076 Tubingen, Germany
关键词
D O I
10.1203/01.pdr.0000127022.45831.54
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The cause of sudden infant death syndrome (SIDS) is an unresolved problem of high relevance. Previous studies indicate a role of infections. In our prospective study, we investigated the frequency of virus-induced myocardial affections in SIDS. Postmortem samples from SIDS victims and control subjects were investigated prospectively. Pediatric cases of unnatural death served as controls. Samples were studied for enteroviruses, adenoviruses, parvovirus B19, and Epstein-Barr Virus applying PCR. Immunohistochemical investigations for inflammatory cells, the necrosis marker C5b-9((m))) complement complex, and the enteroviral capsid protein VP1 were performed. Overall. 62 SIDS victims were studied. As controls, 11 infants were enrolled. Enteroviruses were detected in 14 (22.5%), adenoviruses in 2 (3.2%), Epstein-Barr viruses in 3 (4.8%), and parvovirus B19 in 7 (11.2%) cases of SIDS. Control group samples were completely Virus negative. Compared with controls, immunohistochemical investigations partially revealed a significant increase in the number of T lymphocytes in SIDS myocardial samples (p < 0.05). Furthermore. cases with elevated numbers of leukocytes and macrophages. miicrofocal C5b-9((m))(+) necroses, and enteroviral VP1 capsid protein within the myocardium were detected. Applying a comprehensive combination of molecular and immunohistochemical techniques, our results demonstrate a clearly higher prevalence of viral myocardial affections in SIDS. Our results emphasize the importance of PCR-based diagnosis of viral myocardial affections. We suggest preliminary criteria for cellular immunohistochemical diagnosis of viral myocardial affections derived from our findings. For future investigations in SIDS, we suggest a comprehensive approach that includes PCR and immunohistochemistry. Our results offer novel strategies for diagnosis of pediatric myocardial viral affections.
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页码:947 / 952
页数:6
相关论文
共 30 条
[1]  
ARETZ HT, 1987, HUM PATHOL, V18, P619
[2]   Enteroviral protease 2A directly cleaves dystrophin and is inhibited by a dystrophin-based substrate analogue [J].
Badorff, C ;
Berkely, N ;
Mehrotra, S ;
Talhouk, JW ;
Rhoads, RE ;
Knowlton, KU .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (15) :11191-11197
[3]  
BENEZRA J, 1991, J HISTOCHEM CYTOCHEM, V39, P351, DOI 10.1177/39.3.1704393
[4]   Isolation of a common receptor for coxsackie B viruses and adenoviruses 2 and 5 [J].
Bergelson, JM ;
Cunningham, JA ;
Droguett, G ;
KurtJones, EA ;
Krithivas, A ;
Hong, JS ;
Horwitz, MS ;
Crowell, RL ;
Finberg, RW .
SCIENCE, 1997, 275 (5304) :1320-1323
[5]   HUMAN PARVOVIRUS-B19 INFECTIONS - ROUTINE DIAGNOSIS BY A NEW NESTED POLYMERASE CHAIN-REACTION ASSAY [J].
CASSINOTTI, P ;
WEITZ, M ;
SIEGL, G .
JOURNAL OF MEDICAL VIROLOGY, 1993, 40 (03) :228-234
[6]   QUANTITATIVE-EVALUATION OF INFLAMMATION IN BIOPSY SPECIMENS FROM IDIOPATHICALLY FAILING OR IRRITABLE HEARTS - EXPERIENCE IN 80 PEDIATRIC AND ADULT PATIENTS [J].
CASSLING, RS ;
LINDER, J ;
SEARS, TD ;
WALLER, BF ;
ROGLER, WC ;
WILSON, JE ;
KUGLER, JD ;
KAY, DH ;
DILLON, JC ;
SLACK, JD ;
MCMANUS, BM .
AMERICAN HEART JOURNAL, 1985, 110 (04) :713-720
[7]   EBNA-1 gene sequences in Brazilian and American patients with Hodgkin's disease [J].
Chang, KL ;
Chen, YY ;
Chen, WG ;
Hayashi, K ;
Bacchi, C ;
Bacchi, M ;
Weiss, LM .
BLOOD, 1999, 94 (01) :244-250
[8]   Histologic and in situ viral findings in the myocardium in cases of sudden, unexpected death [J].
Cioc, AM ;
Nuovo, GJ .
MODERN PATHOLOGY, 2002, 15 (09) :914-922
[9]  
Dettmeyer R, 2003, J FORENSIC SCI, V48, P183
[10]   Coxsackie B3 myocarditis in 4 cases of suspected sudden infant death syndrome: Diagnosis by immunohistochemical and molecular-pathologic investigations [J].
Dettmeyer, R ;
Baasner, A ;
Schlamann, M ;
Haag, C ;
Madea, B .
PATHOLOGY RESEARCH AND PRACTICE, 2002, 198 (10) :689-696