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Molecular mechanisms of Zika virus teratogenesis from animal studies: a systematic review protocol

机译:动物研究中Zika病毒畸胎发生的分子机制:系统审查方案

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摘要

Abstract Background Due to the diversity of studies in animal models reporting that molecular mechanisms are involved in the teratogenic effect of the Zika virus (ZIKV), the objective of the present study is to evaluate the methodological quality of these studies, as well as to demonstrate which genes and which molecular pathways are affected by ZIKV in different animal models. Methods This search will be performed in four databases: PubMed/MEDLINE, EMBASE, Web of Science, and Scopus, as well as in the grey literature. The studies selection process will be reported through the PRISMA Statement diagram model. All studies describing the molecular mechanisms possibly involved in the development of malformations caused by embryonic/fetal ZIKV exposure in animal models with an appropriate control group and methodology will be included (including, for instance, randomized and non-randomized studies). All animals used as experimental models for ZIKV teratogenesis may be included as long as exposure to the virus occurred during the embryonic/fetal period. From the selected studies, data will be extracted using a previously prepared standard form. Bias risk evaluation will be conducted following the SYRCLE’s Risk of Bias tool. All data obtained will be tabulated and organized by outcomes (morphological and molecular). Discussion With the proposed systematic review, we expect to present results about the methodological quality of the published studies with animal models that investigated the molecular mechanisms involved in the teratogenic effect of ZIKV, as well as to show the studies with greater reliability. Systematic review registration PROSPERO CRD42019157316
机译:摘要背景由于在动物模型中报告说,分子机制参与寨卡病毒(ZIKV)的致畸作用研究的多样性,本研究的目的是评估这些研究的方法学质量,以及证明哪些基因和分子通路被ZIKV在不同的动物模型的影响。方法本搜索将在四个数据库进行:考研/ MEDLINE,文摘,科学网,和Scopus,以及在灰色文献。该研究选择过程将通过PRISMA声明图模型进行报告。所有描述中可能涉及的致在动物模型中与适当的对照组和方法胚胎/胎儿ZIKV曝光畸形的发展的分子机制的研究将包含(包括,例如,随机化和非随机研究)。作为实验模型ZIKV致畸所有的动物都可以被列入只要接触病毒在胚胎/胎儿时期发生。从选定的研究中,数据将使用预先准备的标准形式来提取。偏差的风险评估将以下偏压工具的SYRCLE的风险进行。所获得的所有数据将被制成表格和通过的结果(形态学和分子)进行组织。讨论随着所提出的系统回顾,我们希望有关与动物模型公布的研究,研究涉及ZIKV的致畸作用的分子机制的方法学质量目前的结果,以及表现出更大的可靠性研究。系统评价注册PROSPERO CRD42019157316

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