Instituto Aggeu Magalhães, Programa de Pós-Graduação em Saúde Pública, Recife, PE, Brasil.
Universidade de Pernambuco, Pós-Graduação em Ciências da Saúde, Recife, PE, Brasil.
Rev Soc Bras Med Trop. 2024 Jul 29;57:e00301. doi: 10.1590/0037-8682-0153-2024. eCollection 2024.
This review aimed to provide an update on the morphological and/or functional abnormalities related to congenital Zika virus (ZIKV) infection, based on primary data from studies conducted in Brazil since 2015. During the epidemic years (2015-2016), case series and pediatric cohort studies described several birth defects, including severe and/or disproportionate microcephaly, cranial bone overlap, skull collapse, congenital contractures (arthrogryposis and/or clubfoot), and visual and hearing abnormalities, as part of the spectrum of Congenital Zika Syndrome (CZS). Brain imaging abnormalities, mainly cortical atrophy, ventriculomegaly, and calcifications, serve as structural markers of CZS severity. Most case series and cohorts of microcephaly have reported the co-occurrence of epilepsy, dysphagia, orthopedic deformities, motor function impairment, cerebral palsy, and urological impairment. A previous large meta-analysis conducted in Brazil revealed that a confirmed ZIKV infection during pregnancy was associated with a 4% risk of microcephaly. Additionally, one-third of children showed at least one abnormality, predominantly identified in isolation. Studies examining antenatally ZIKV-exposed children without detectable abnormalities at birth reported conflicting neurodevelopmental results. Therefore, long-term follow-up studies involving pediatric cohorts with appropriate control groups are needed to address this knowledge gap. We recognize the crucial role of a national network of scientists collaborating with international research institutions in understanding the lifelong consequences of congenital ZIKV infection. Additionally, we highlight the need to provide sustainable resources for research and development to reduce the risk of future Zika outbreaks.
本综述旨在根据 2015 年以来巴西开展的研究中的原始数据,提供有关先天性寨卡病毒(ZIKV)感染相关形态和/或功能异常的最新信息。在流行年份(2015-2016 年),病例系列和儿科队列研究描述了几种出生缺陷,包括严重和/或不成比例的小头畸形、颅骨重叠、颅骨塌陷、先天性挛缩(关节挛缩和/或马蹄足)以及视觉和听力异常,这些都是先天性寨卡综合征(CZS)的一部分。脑影像学异常,主要是皮质萎缩、脑室扩大和钙化,是 CZS 严重程度的结构标志物。大多数小头畸形病例系列和队列都报告了癫痫、吞咽困难、骨科畸形、运动功能障碍、脑瘫和泌尿系统损伤的共同发生。巴西之前进行的一项大型荟萃分析表明,怀孕期间确诊的 ZIKV 感染与小头畸形的风险增加 4%相关。此外,三分之一的儿童至少存在一种异常,主要是孤立存在的异常。对出生时未检测到异常的产前 ZIKV 暴露儿童进行的研究报告了相互矛盾的神经发育结果。因此,需要对涉及适当对照组的儿科队列进行长期随访研究,以填补这一知识空白。我们认识到一个由与国际研究机构合作的科学家组成的国家网络在理解先天性 ZIKV 感染的终身后果方面的关键作用。此外,我们强调需要为研究和开发提供可持续的资源,以降低未来寨卡病毒爆发的风险。