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Molecular mechanisms of Zika virus teratogenesis from animal studies: a systematic review protocol
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 w...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164069/ https://www.ncbi.nlm.nih.gov/pubmed/34051864 http://dx.doi.org/10.1186/s13643-021-01713-6 |
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author | Wachholz, Gabriela Elis do Amaral Gomes, Julia Boquett, Juliano André Vianna, Fernanda Sales Luiz Schuler-Faccini, Lavínia Fraga, Lucas Rosa |
author_facet | Wachholz, Gabriela Elis do Amaral Gomes, Julia Boquett, Juliano André Vianna, Fernanda Sales Luiz Schuler-Faccini, Lavínia Fraga, Lucas Rosa |
author_sort | Wachholz, Gabriela Elis |
collection | PubMed |
description | 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 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13643-021-01713-6. |
format | Online Article Text |
id | pubmed-8164069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81640692021-06-01 Molecular mechanisms of Zika virus teratogenesis from animal studies: a systematic review protocol Wachholz, Gabriela Elis do Amaral Gomes, Julia Boquett, Juliano André Vianna, Fernanda Sales Luiz Schuler-Faccini, Lavínia Fraga, Lucas Rosa Syst Rev Protocol 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 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13643-021-01713-6. BioMed Central 2021-05-29 /pmc/articles/PMC8164069/ /pubmed/34051864 http://dx.doi.org/10.1186/s13643-021-01713-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Protocol Wachholz, Gabriela Elis do Amaral Gomes, Julia Boquett, Juliano André Vianna, Fernanda Sales Luiz Schuler-Faccini, Lavínia Fraga, Lucas Rosa Molecular mechanisms of Zika virus teratogenesis from animal studies: a systematic review protocol |
title | Molecular mechanisms of Zika virus teratogenesis from animal studies: a systematic review protocol |
title_full | Molecular mechanisms of Zika virus teratogenesis from animal studies: a systematic review protocol |
title_fullStr | Molecular mechanisms of Zika virus teratogenesis from animal studies: a systematic review protocol |
title_full_unstemmed | Molecular mechanisms of Zika virus teratogenesis from animal studies: a systematic review protocol |
title_short | Molecular mechanisms of Zika virus teratogenesis from animal studies: a systematic review protocol |
title_sort | molecular mechanisms of zika virus teratogenesis from animal studies: a systematic review protocol |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164069/ https://www.ncbi.nlm.nih.gov/pubmed/34051864 http://dx.doi.org/10.1186/s13643-021-01713-6 |
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