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Published on: December 3, 2021
Role of virus-induced myocardial affections in sudden infant death syndrome: a prospective postmortem study
Reinhard Dettmeyer1, Anne Baasner, Marc Schlamann
1Department of Forensic Medicine, University of Bonn, Stiftsplatz 12, D-53111 Bonn, Germany. rdettmey@uni-bonn.de
Abstract:
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.
Insights
Sudden Infant Death Syndrome (SIDS) may be linked to viral heart infections. This study found viruses, particularly enteroviruses, in SIDS cases, suggesting a role for viral myocarditis in SIDS.
Area of Science:
- Pathology
- Virology
- Pediatrics
Background:
- Sudden Infant Death Syndrome (SIDS) remains a significant pediatric concern with an unknown etiology.
- Previous research suggests infectious agents may contribute to SIDS.
- Viral infections affecting the heart (myocardial affections) are a potential, under-investigated factor in SIDS.
Purpose of the Study:
- To investigate the frequency and characteristics of virus-induced myocardial affections in SIDS victims.
- To compare findings in SIDS cases with a control group of infants who died unnaturally.
- To establish diagnostic criteria for viral myocarditis in SIDS using molecular and immunohistochemical methods.
Main Methods:
- Prospective analysis of postmortem myocardial samples from 62 SIDS victims and 11 control infants.
- Polymerase Chain Reaction (PCR) to detect enteroviruses, adenoviruses, parvovirus B19, and Epstein-Barr virus.
- Immunohistochemistry to identify inflammatory cells, necrosis marker C5b-9((m)), and enteroviral capsid protein VP1.
Main Results:
- Viruses were detected in SIDS cases (enteroviruses 22.5%, adenoviruses 3.2%, Epstein-Barr virus 4.8%, parvovirus B19 11.2%), while control samples were virus-negative.
- SIDS myocardial samples showed increased T lymphocytes, leukocytes, macrophages, microfocal necroses, and enteroviral VP1.
- A combination of PCR and immunohistochemistry revealed a higher prevalence of viral myocardial affections in SIDS.
Conclusions:
- This study demonstrates a significant association between viral myocardial affections and SIDS.
- PCR-based diagnosis and immunohistochemistry are crucial for identifying viral myocarditis in SIDS.
- Findings provide novel strategies for diagnosing pediatric viral myocardial affections and suggest criteria for SIDS diagnosis.
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