Dettmeyer Reinhard, Baasner Anne, Schlamann Marc, Padosch Stephan A, Haag Claudia, Kandolf Reinhard, Madea Burkhard
Department of Forensic Medicine, University of Bonn, Stiftsplatz 12, D-53111 Bonn, Germany.
Pediatr Res. 2004 Jun;55(6):947-52. doi: 10.1203/01.pdr.0000127022.45831.54.
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, microfocal 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.
婴儿猝死综合征(SIDS)的病因是一个尚未解决的高度相关问题。先前的研究表明感染起了一定作用。在我们的前瞻性研究中,我们调查了SIDS中病毒诱导的心肌病变的发生率。对SIDS受害者和对照受试者的尸检样本进行了前瞻性研究。非自然死亡的儿科病例作为对照。应用聚合酶链反应(PCR)对样本进行肠道病毒、腺病毒、细小病毒B19和爱泼斯坦-巴尔病毒检测。对炎症细胞、坏死标志物C5b-9(m)补体复合物和肠道病毒衣壳蛋白VP1进行免疫组织化学研究。总体而言,研究了62例SIDS受害者。作为对照,纳入了11名婴儿。在14例(22.5%)SIDS病例中检测到肠道病毒,2例(3.2%)检测到腺病毒,3例(4.8%)检测到爱泼斯坦-巴尔病毒,7例(11.2%)检测到细小病毒B19。对照组样本病毒检测均为阴性。与对照组相比,免疫组织化学研究部分显示SIDS心肌样本中T淋巴细胞数量显著增加(p<0.05)。此外,还检测到心肌内白细胞和巨噬细胞数量增加、微灶性C5b-9(m)(+)坏死以及肠道病毒VP1衣壳蛋白的病例。应用分子和免疫组织化学技术的综合组合,我们的结果表明SIDS中病毒心肌病变的患病率明显更高。我们的结果强调了基于PCR诊断病毒心肌病变的重要性。我们根据研究结果提出了病毒心肌病变细胞免疫组织化学诊断的初步标准。对于未来SIDS的研究,我们建议采用包括PCR和免疫组织化学的综合方法。我们的结果为儿科心肌病毒感染的诊断提供了新策略。