Asturias Edwin J, Connery Amy K, Olson Daniel, Lamb Molly M, Paniagua-Avila Alejandra, Anderson Evan J, Focht Chris, Colbert Alison M, Natrajan Muktha, Waggoner Jesse J, Scherer Erin, Calvimontes D Mirella, Bolaños Guillermo A, Bauer Desirée, Arroyave Paola, Hernández Sara, Martinez Maria A, Ralda Aida V, Rojop Neudy, Barrios Edgar E, Chacon Andrea, Dempsey Walla, Tomashek Kay M, Keitel Wendy A, El Sahly Hana M, Muñoz Flor M
From the Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado.
Center for Global Health or Department of Epidemiology, Colorado School of Public Health, Aurora, Colorado.
Pediatr Infect Dis J. 2025 Apr 1;44(4):290-298. doi: 10.1097/INF.0000000000004646. Epub 2024 Dec 6.
Prenatal Zika virus (ZIKV) infection leads to microcephaly and adverse neurodevelopment. The effects of postnatal ZIKV infection on the developing brain are unknown. We assessed the neurodevelopmental outcomes of children exposed postnatally during the ZIKV epidemic.
A prospective study enrolled infants 0-3 months of age and their mothers, and children 1.5-3.5 years of age in rural Guatemala from 2017 and were followed for 12 months until 2019. Neurodevelopment was evaluated using the Mullen Scales of Early Learning (MSEL). ZIKV and dengue virus (DENV) infections were identified by polymerase chain reaction (PCR) using active surveillance. Serological analyses, stratified by age group flavivirus serostatus at enrollment, were conducted using a focus reduction neutralization test.
Of 1371 enrolled participants, 1187 (86.6%) completed the study. No PCR-confirmed ZIKV infections were identified during the study period. One-third of 1.5-3.5-year-old children were ZIKV-seropositive at enrollment (likely postnatal infection). Twenty participants (5.8%) tested positive for DENV by PCR (11 infants, 5 children and 4 mothers); 15 (75%) were DENV-3 infections and 5 were DENV-2. The incidence of DENV infection in infants was 2.6%. No significant differences in MSEL scores were found between infants born seropositive versus seronegative for ZIKV or DENV. DENV seropositivity at enrollment in 1.5-5-year-old children was associated with lower MSEL scores for fine motor, visual reception and language, and microcephaly at 12 months versus seronegative children (all P < 0.05).
Postnatal ZIKV infection in children from rural Guatemala was not associated with worse neurodevelopmental outcomes. DENV seropositivity was associated with a higher risk of microcephaly in infants and worse neurodevelopmental outcomes in children.
产前寨卡病毒(ZIKV)感染会导致小头畸形和不良神经发育。产后ZIKV感染对发育中大脑的影响尚不清楚。我们评估了寨卡病毒流行期间产后暴露儿童的神经发育结局。
一项前瞻性研究纳入了危地马拉农村地区2017年0至3个月大的婴儿及其母亲,以及1.5至3.5岁的儿童,并随访12个月直至2019年。使用莫伦早期学习量表(MSEL)评估神经发育。通过主动监测,采用聚合酶链反应(PCR)鉴定ZIKV和登革病毒(DENV)感染。使用焦点减少中和试验进行血清学分析,按入组时黄病毒血清状态的年龄组分层。
在1371名入组参与者中,1187名(86.6%)完成了研究。研究期间未发现PCR确诊的ZIKV感染。1.5至3.5岁儿童中有三分之一在入组时ZIKV血清学呈阳性(可能为产后感染)。20名参与者(5.8%)PCR检测DENV呈阳性(11名婴儿、5名儿童和4名母亲);15例(75%)为DENV-3感染,5例为DENV-2感染。婴儿中DENV感染的发生率为2.6%。在ZIKV或DENV血清学呈阳性与呈阴性的婴儿之间,未发现MSEL评分有显著差异。1.5至5岁儿童入组时DENV血清学呈阳性与精细运动、视觉接受和语言方面较低的MSEL评分以及12个月时小头畸形有关,与血清学呈阴性的儿童相比(所有P<0.05)。
危地马拉农村地区儿童产后ZIKV感染与更差的神经发育结局无关。DENV血清学呈阳性与婴儿小头畸形风险较高以及儿童神经发育结局较差有关。