Another piece of the Zika puzzle: assessing the associated factors to microcephaly in a systematic review and meta-analysis.


Journal

BMC public health
ISSN: 1471-2458
Titre abrégé: BMC Public Health
Pays: England
ID NLM: 100968562

Informations de publication

Date de publication:
01 Jun 2020
Historique:
received: 01 10 2019
accepted: 18 05 2020
entrez: 4 6 2020
pubmed: 4 6 2020
medline: 3 11 2020
Statut: epublish

Résumé

Although it is known that Zika virus (ZIKV) infection during pregnancy may lead to microcephaly in the fetus, the prognostic factors associated with this tragic disorder remain unclear. We conducted a systematic review and meta-analysis to assess the prognostic factors associated with the incidence of microcephaly in congenital ZIKV infection. We conducted a comprehensive search in Ovid MEDLINE, Ovid MEDLINE (R) Epub ahead of print, Embase, Embase Classic, Web of Science, CINAHL, Cochrane CENTRAL, LILACS, and various thesis databases to identify human studies reporting microcephaly associated with congenital ZIKV infection. We requested primary data from the authors of the included studies to calculate summary estimates and conduct the meta-analysis of the most prevalent factors. We screened 4106 titles and abstracts, and identified 12 studies for inclusion in the systematic review. The assessment of ZIKV infection and the definition of microcephaly varied among studies. A total of 6154 newborns/fetuses were enrolled; of those, 1120 (18.20%) had a diagnostic of ZIKV infection, of which 509 (45.45%) were diagnosed with microcephaly. Nine studies addressed the link between congenital ZIKV infection and neurological findings in newborns/fetuses. Half of the studies provided primary data. Three out of 11 factors of interest seem to be prognostic factors of microcephaly: infant's sex - males compared to females: Relative Risk (RR) 1.30, 95% Confidence Interval (95% CI) 1.14 to 1.49; the stage of pregnancy when infection occurred - infection in the first trimester of pregnancy compared to infection at other stages of pregnancy: RR 1.41, 95% CI 1.09 to 1.82; and asymptomatic infection compared to symptomatic infection during pregnancy: RR 0.68; 95% CI 0.60 to 0.77. Our findings support the female-biased resistance hypothesis and reinforce the risk associated with the stage of pregnancy when ZIKV infection occurs. Continued surveillance of ZIKV infection during pregnancy is needed to identify additional factors that could contribute to developing microcephaly in affected fetuses. This systematic review was registered with the International Prospective Register of Systematic Reviews (PROSPERO), registration no. CRD 42018088075.

Sections du résumé

BACKGROUND BACKGROUND
Although it is known that Zika virus (ZIKV) infection during pregnancy may lead to microcephaly in the fetus, the prognostic factors associated with this tragic disorder remain unclear. We conducted a systematic review and meta-analysis to assess the prognostic factors associated with the incidence of microcephaly in congenital ZIKV infection.
METHODS METHODS
We conducted a comprehensive search in Ovid MEDLINE, Ovid MEDLINE (R) Epub ahead of print, Embase, Embase Classic, Web of Science, CINAHL, Cochrane CENTRAL, LILACS, and various thesis databases to identify human studies reporting microcephaly associated with congenital ZIKV infection. We requested primary data from the authors of the included studies to calculate summary estimates and conduct the meta-analysis of the most prevalent factors.
RESULTS RESULTS
We screened 4106 titles and abstracts, and identified 12 studies for inclusion in the systematic review. The assessment of ZIKV infection and the definition of microcephaly varied among studies. A total of 6154 newborns/fetuses were enrolled; of those, 1120 (18.20%) had a diagnostic of ZIKV infection, of which 509 (45.45%) were diagnosed with microcephaly. Nine studies addressed the link between congenital ZIKV infection and neurological findings in newborns/fetuses. Half of the studies provided primary data. Three out of 11 factors of interest seem to be prognostic factors of microcephaly: infant's sex - males compared to females: Relative Risk (RR) 1.30, 95% Confidence Interval (95% CI) 1.14 to 1.49; the stage of pregnancy when infection occurred - infection in the first trimester of pregnancy compared to infection at other stages of pregnancy: RR 1.41, 95% CI 1.09 to 1.82; and asymptomatic infection compared to symptomatic infection during pregnancy: RR 0.68; 95% CI 0.60 to 0.77.
CONCLUSION CONCLUSIONS
Our findings support the female-biased resistance hypothesis and reinforce the risk associated with the stage of pregnancy when ZIKV infection occurs. Continued surveillance of ZIKV infection during pregnancy is needed to identify additional factors that could contribute to developing microcephaly in affected fetuses.
PROTOCOL REGISTRATION BACKGROUND
This systematic review was registered with the International Prospective Register of Systematic Reviews (PROSPERO), registration no. CRD 42018088075.

Identifiants

pubmed: 32487247
doi: 10.1186/s12889-020-08946-5
pii: 10.1186/s12889-020-08946-5
pmc: PMC7266116
doi:

Types de publication

Comparative Study Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

827

Subventions

Organisme : Ministério da Educação
ID : CAPES/PDSE 88881.133664/2016-01

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Auteurs

Luciana Guerra Gallo (LG)

Postgraduate Program in Tropical Medicine, University of Brasilia, Brasilia, Brazil.
Department of Obstetrics and Gynecology and Department of Public Health Sciences, Queen's University, Kingston, Canada.

Jorge Martinez-Cajas (J)

Department of Medicine, Queen's University, Kingston, Canada.

Henry Maia Peixoto (HM)

Postgraduate Program in Tropical Medicine, University of Brasilia, Brasilia, Brazil.

Ana Carolina Esteves da Silva Pereira (ACEDS)

Program of Evidence for Policies and Health Technologies, Oswaldo Cruz Foundation, Brasilia, Brazil.

Jillian E Carter (JE)

Department of Obstetrics and Gynecology and Department of Public Health Sciences, Queen's University, Kingston, Canada.

Sandra McKeown (S)

Bracken Health Sciences Library, Queen's University, Kingston, Canada.

Bruno Schaub (B)

Centre Pluridisciplinaire de Diagnostic Prénatal de le Martinique, Maison de la Femme, de la Mère et de l'Enfant, University Hospital of Martinique, Fort-de-France, Martinique.

Camila V Ventura (CV)

Department of Scientific Investigation, Altino Ventura Foundation, Recife, Brazil.

Giovanny Vinícius Araújo de França (GVA)

Brazilian Ministry of Health, Brasilia, Brazil.

Léo Pomar (L)

Materno-fetal and Obstetrics Research Unit, Département "Femme-Mère Enfant", University Hospital, Lausanne, Switzerland.
Department of Obstetrics and Gynaecology, Centre Hospitalier de l'Ouest Guyanais Franck Joly, Saint-Laurent-du-Maroni, French Guiana.

Liana O Ventura (LO)

Department of Pediatric Ophthalmology and Strabismus, Altino Ventura Foundation, Recife, Brazil.

Vivek R Nerurkar (VR)

Department of Tropical Medicine, Medical Microbiology and Pharmacology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, USA.

Wildo Navegantes de Araújo (WN)

Postgraduate Program in Tropical Medicine, University of Brasilia, Brasilia, Brazil.

Maria P Velez (MP)

Department of Obstetrics and Gynecology and Department of Public Health Sciences, Queen's University, Kingston, Canada. maria.velez@queensu.ca.

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