Investigating the role of cytomegalovirus as a cause of stillbirths and child deaths in low and middle-income countries through postmortem minimally invasive tissue sampling.

Sithembiso Velaphi ORCID logo ; Zachary J Madewell ORCID logo ; Beth Tippett-Barr ORCID logo ; Dianna M Blau ORCID logo ; Emily A Rogena ; Sanjay G Lala ; Sana Mahtab ; Peter J Swart ; Victor Akelo ; Dickens Onyango ; +28 more... Kephas Otieno ; Emily A Rogena ; Joyce A Were ORCID logo ; Quique Bassat ORCID logo ; Carla Carrilho ; Inacio Mandomando ORCID logo ; David Torres-Fernandez ORCID logo ; Rosauro Varo ORCID logo ; Ronita Luke ; Francis Moses ; Philip Nwajiobi-Princewill ; Ikechukwu Udo Ogbuanu ; Julius Ojulong ; Shams El Arifeen ; Emily S Gurley ; Nega Assefa ORCID logo ; Letta Gedefa ; Lola Madrid ; J Anthony G Scott ORCID logo ; Henok Wale ; Jane Juma ; Adama Mamby Keita ORCID logo ; Karen L Kotloff ; Samba O Sow ; Milagritos D Tapia ; Portia Mutevedzi ; Cynthia G Whitney ORCID logo ; Shabir A Madhi ; (2025) Investigating the role of cytomegalovirus as a cause of stillbirths and child deaths in low and middle-income countries through postmortem minimally invasive tissue sampling. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. ciaf098-. ISSN 1058-4838 DOI: 10.1093/cid/ciaf098
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BACKGROUND: There is paucity of information on the role of cytomegalovirus (CMV) infection as a cause of stillbirths or childhood deaths in low-and middle-income countries (LMICs). We investigated attribution of CMV-disease in the causal pathway to stillbirths and deaths in children <5 years of age in seven LMICs participating in the Child Health and Mortality Prevention Surveillance (CHAMPS) network. METHODS: We analyzed stillbirths and decedents enrolled between December 2016 and July 2023. Deaths were investigated using post-mortem minimally invasive tissue sampling with histopathology and molecular diagnostic investigations of tissues and body fluids, along with review of clinical records. Multi-disciplinary expert panels reviewed findings and reported on the causal pathway to death. RESULTS: CMV was detected in 19.5%(1140/5841) of all evaluated deaths, including 5.0% (111/2204), 6.2% (139/2229), 41.2% (107/260), 68.1%(323/474) and 68.2%(460/674) of stillbirths, neonates (deaths 0-<28 days postnatal), young infants (28-<90 days), older infants (90-<365 days) and children (12-<60 months), respectively. CMV-disease was attributed in the causal pathway to death in 0.9%(20/2204) of stillbirths, 0.8%(17/2229) of neonates, 13.1% (34/260) of young infants, 9.7%(46/474) of older infants and 3.3%(22/674) of children. Decedents with CMV-disease compared with those without CMV-disease in the causal pathway, were more likely to have severe microcephaly (38.2% vs. 21.1%; aOR 2.2, 95%CI: 1.3-3.6) and HIV-infected (36.9% vs. 6.2%; aOR: 10.9, 95%CI: 6.5-18.5). CONCLUSIONS: CMV-disease is an important contributor to deaths during infancy and childhood and is often associated with severe microcephaly and HIV-infection. Improving management of CMV in HIV-infected children and a vaccine to prevent CMV are needed interventions.

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