Velaphi Sithembiso, Madewell Zachary J, Tippett-Barr Beth, Blau Dianna M, Rogena Emily A, Lala Sanjay G, Mahtab Sana, Swart Peter J, Akelo Victor, Onyango Dickens, Otieno Kephas, Rogena Emily A, Were Joyce A, Bassat Quique, Carrilho Carla, Mandomando Inacio, Torres-Fernandez David, Varo Rosauro, Luke Ronita, Moses Francis, Nwajiobi-Princewill Philip, Ogbuanu Ikechukwu Udo, Ojulong Julius, El Arifeen Shams, Gurley Emily S, Assefa Nega, Gedefa Letta, Madrid Lola, Scott J Anthony G, Wale Henok, Juma Jane, Keita Adama Mamby, Kotloff Karen L, Sow Samba O, Tapia Milagritos D, Mutevedzi Portia, Whitney Cynthia G, Madhi Shabir A
Department of Paediatrics, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Global Health Center, US Centers for Disease Control and Prevention, Atlanta, USA.
Clin Infect Dis. 2025 Mar 10. doi: 10.1093/cid/ciaf098.
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.
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.
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).
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.
在低收入和中等收入国家(LMICs),关于巨细胞病毒(CMV)感染作为死产或儿童死亡原因的信息匮乏。我们调查了参与儿童健康与死亡率预防监测(CHAMPS)网络的7个低收入和中等收入国家中,CMV疾病在5岁以下儿童死产和死亡因果路径中的归因。
我们分析了2016年12月至2023年7月期间登记的死产和死亡病例。通过尸检微创组织采样、组织病理学以及对组织和体液的分子诊断研究,并结合临床记录回顾对死亡病例进行调查。多学科专家小组审查研究结果并报告死亡的因果路径。
在所有评估的死亡病例中,19.5%(1140/5841)检测到CMV,其中死产、新生儿(出生后0至<28天死亡)、幼儿(28至<90天)、大龄婴儿(90至<365天)和儿童(12至<60个月)中检测到CMV的比例分别为5.0%(111/2204)、6.2%(139/2229)、41.2%(107/260)、68.1%(323/474)和68.2%(460/674)。在因果路径中,CMV疾病归因于死亡的比例在死产中为0.9%(20/2204),新生儿中为0.8%(17/2229),幼儿中为13.1%(34/260),大龄婴儿中为9.7%(46/474),儿童中为3.3%(22/674)。与因果路径中无CMV疾病的死者相比,有CMV疾病的死者更可能患有严重小头畸形(38.2%对21.1%;调整后比值比[aOR]2.2,95%置信区间[CI]:1.3 - 3.6)和感染HIV(36.9%对6.2%;aOR:10.9,95%CI:6.5 - 18.5)。
CMV疾病是婴儿期和儿童期死亡的重要原因,且常与严重小头畸形和HIV感染相关。需要采取干预措施改善对感染HIV儿童的CMV管理以及研发预防CMV的疫苗。