CC BY-NC-ND 4.0 · Geburtshilfe Frauenheilkd 2020; 80(01): 60-65
DOI: 10.1055/a-0972-2052
GebFra Science
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Zika Virus and Pregnancy: Association between Acute Infection and Microcephaly in Newborns in the State of Rio de Janeiro, Brazil

Zikavirus und Schwangerschaft: Assoziation zwischen akuter Infektion und Mikrozephalie bei Neugeborenen im Bundesstaat Rio de Janeiro, Brasilien
Alessandra Mendelski Pereira
1   Perinatal Unit, State University of Rio de Janeiro (UERJ), Rio de Janeiro-RJ, Brazil
,
Edward Araujo Júnior
2   Department of Obstetrics, Paulista School of Medicine – Federal University of São Paulo (EPM-UNIFESP), São Paulo-SP, Brazil
3   Medical course, Municipal University of São Caetano do Sul (USCS), São Paulo-SP, Brazil
,
Heron Werner
4   Department of Radiology, Clínica de Diagnóstico por Imagem (CPDI), Rio de Janeiro-RJ, Brazil
,
Denise Leite Maia Monteiro
1   Perinatal Unit, State University of Rio de Janeiro (UERJ), Rio de Janeiro-RJ, Brazil
› Author Affiliations
Further Information

Publication History

received 20 June 2019
revised 06 July 2019

accepted 09 July 2019

Publication Date:
13 January 2020 (online)

Abstract

Introduction Aim of the study was to evaluate the association between microcephaly and acute infection with Zika virus (ZIKV) in pregnant women in the state of Rio de Janeiro, Brazil. Infection was confirmed by laboratory testing.

Materials and Methods A cross-sectional retrospective study of pregnant women with symptoms occurring between 2015 and 2016 suggestive of acute ZIKV infection was carried out, with confirmation of infection done by blood or urine RT-PCR. The relative proportions of categorical variables were calculated for two distinct groups: pregnant women whose newborns had microcephaly and pregnant women who gave birth to infants without microcephaly. Confidence intervals with a 95% level of agreement were estimated for the relative ratios.

Results A total of 1609 pregnant women with a mean age of 26.4 ± 6.5 years were evaluated. As regards the time of acute infection, 19.6% (316) of cases occurred in the first trimester of pregnancy. Nineteen (76%) of the 25 cases with microcephaly (1.5%) were associated with an infection contracted in the first trimester of pregnancy (p < 0.001, OR = 13.7, 95% CI: 5.6 – 37.7). 48% (12/25) of the newborns with microcephaly had a birth weight of < 2500 grams, while only 7% (116/1597) of the group of newborns without microcephaly had a similarly low birth weight (p < 0.001, OR = 11.7, 95% CI: 5.2 – 26.2). Logistic regression showed that a birth weight of < 2500 g (OR = 12.54) and ZIKV infection in the first trimester of pregnancy (OR = 14.05) were associated with microcephaly (area under ROC curve = 0.86).

Conclusion Acute ZIKV infection in the first trimester of pregnancy and low birth weight are associated with microcephaly.

Zusammenfassung

Einleitung Ziel dieser Studie war es, die Assoziation zwischen Mikrozephalie und akuter Infektion mit Zikavirus (ZIKV) bei schwangeren Frauen im Bundesstaat Rio de Janeiro, Brasilien zu untersuchen. Die Infektion wurde durch Laboruntersuchungen bestätigt.

Material und Methoden Es wurde eine retrospektive Querschnittsstudie von schwangeren Frauen mit Symptomen, die zwichen 2015 und 2016 auftraten und die auf eine Infektion mit ZIKV hindeuteten, durchgeführt. Die Infektion wurde mittels RT-PCR von Blut- bzw. Urinproben bestätigt. Die relativen Anteile der kategorischen Variablen wurden für 2 verschiedenen Gruppen kalkuliert: schwangere Frauen, die Neugeborene mit Mikrozephalie zur Welt brachten, und schwangere Frauen, deren Kinder keine Mikrozephalie aufwiesen. Die 95%-Konfidenzintervalle für die relativen Anteile wurden geschätzt.

Ergebnisse Insgesamt wurden 1609 schwangere Frauen mit einem Durchschnittsalter von 26,4 ± 6,5 Jahren evaluiert. Was den Zeitpunkt der akuten Infektion angeht, stellte sich heraus, dass 19,6% (316) der Infektionen im 1. Schwangerschaftstrimenon aufgetreten waren. Bei 25 Fällen mit Mikrozephalie (1,5%) bestand bei 19 (76%) eine Assoziation mit einer Ansteckung im 1. Trimester der Schwangerschaft (p < 0,001; OR = 13,7; 95%-KI [5,6 – 37,7]). Von den Neugeborenen mit Mikrozephalie hatten 48% (12/25) ein Geburtsgewicht von < 2500 g, wohingegen nur 7% (116/1597) der Neugeborenen in der Gruppe ohne Mikrozephalie ein ähnlich niedriges Geburtsgewicht aufwiesen (p < 0,001; OR = 11,7; 95%-KI [5,2 – 26,2]). Das logistische Regressionsmodell zeigte, dass ein Geburtsgewicht von < 2500 g (OR = 12,54) sowie eine ZIKV-Infektion im 1. Trimenon der Schwangerschaft (OR = 14,05) mit Mikrozephalie assoziiert sind (Fläche unter der ROC-Kurve = 0,86).

Schlussfolgerung Akute Infektion mit ZIKV im 1.  Schwangerschaftstrimester und ein niedriges Geburtsgewicht sind mit dem Auftreten von Mikrozephalie assoziiert.

 
  • References

  • 1 Dick GW. Zika virus. II. Pathogenicity and physical properties. Trans R Soc Trop Med Hyg 1952; 46: 521-534
  • 2 Macnamara FN. Zika virus: a report on three cases of human infection during an epidemic of jaundice in Nigeria. Trans R Soc Trop Med Hyg 1954; 48: 139-145
  • 3 Duffy MR, Chen TH, Hancock WT. et al. Zika Virus outbreak on Yap Island, Federated States of Micronesia. N Engl J Med 2009; 360: 2536-2543
  • 4 Cao-Lorneau VM, Roche C, Teissier A. et al. Zika virus, French Polynesia, South Pacific, 2013. Emerg Infect Dis 2014; 20: 1085-1086
  • 5 Musso D. Zika virus transmission from French Polynesia to Brazil. Emerg Infect Dis 2015; 21: 1887
  • 6 Campos GS, Bandeira AC, Sardi SI. Zika virus outbreak, Bahia, Brazil. Emerg Infect Dis 2015; 21: 1885-1886
  • 7 Faccini LS, Ribeiro ME, Feitosa IML. et al. Possible association between Zika virus infection and microcephaly. MMWR Morb Mortal Wkly Rep 2016; 65: 59-62
  • 8 Oliveira Melo AS, Malinger G, Ximenes R. et al. Zika vírus intrauterine infection causes fetal brain abnormality and microcephaly: tip of the iceberg?. Ultrasound Obstet Gynecol 2016; 47: 6-7
  • 9 Brasil P, Pereira jr. JP, Moreira ME. et al. Zika virus Infection in Pregnant Women in Rio de Janeiro. N Engl J Med 2016; 375: 2321-2334
  • 10 Mehrjardi MZ, Poretti A, Huisman TAG. et al. Neuroimaging findings of congenital Zika virus infection: a pictorial essay. Jpn J Radiol 2017; 35: 89-94
  • 11 Panchaud A, Stojanov M, Ammerdorffer A. et al. Emerging Role of Zika Virus in Adverse Fetal and Neonatal Outcomes. Clin Microbiol 2016; 29: 659-694
  • 12 Pereira AM, Monteiro DLM, Werner H. et al. Zika virus and pregnancy in Brazil: What happened?. J Turk Ger Gynecol Assoc 2018; 19: 39-47
  • 13 Ramalho Rocha YR, Cavalcanti Costa JR, Almeida Costa P. et al. Radiological Characterization of Cerebral Phenotype in Newborn Microcephaly Cases from 2015 Outbreak in Brazil. PLoS Curr 2016; DOI: 10.1371/currents.outbreaks.e854dbf51b8075431a05b39042c00244.
  • 14 Ximenes ASFC, Pires P, Werner H. et al. Neuroimaging findings using transfontanellar ultrasound in newborns with microcephaly: a possible association with congenital Zika virus infection. J Matern Fetal Neonatal Med 2019; 32: 493-501
  • 15 Pires P, Jungmann P, Galvão JM. et al. Neuroimaging findings associated with congenital Zika virus syndrome: case series at the time of first epidemic outbreak in Pernambuco State, Brazil. Childs Nerv Syst 2018; 34: 957-963
  • 16 Werner H, Sodré D, Hygino C. et al. First-trimester intrauterine Zika virus infection and brain pathology: prenatal and postnatal neuroimaging findings. Prenat Diagn 2016; 36: 785-789
  • 17 Araujo Júnior E, Carvalho FH, Tonni G. et al. Prenatal imaging findings in fetal Zika virus infection. Curr Opin Obstet Gynecol 2017; 29: 95-105
  • 18 Carvalho FH, Cordeiro KM, Peixoto AB. et al. Associated ultrasonographic findings in fetuses with microcephaly because of suspected Zika virus (ZIKV) infection during pregnancy. Prenat Diagn 2016; 36: 882-887
  • 19 Castanha PM, Cordeiro MT, Martelli CM. et al. Force of infection of dengue serotypes in a population-based study in the northeast of Brazil. Epidemiol Infect 2013; 141: 1080-1088
  • 20 Hoen B, Schaub B, Funk AL. et al. Pregnancy Outcomes after ZIKV Infection in French Territories in the Americas. N Engl J Med 2018; 378: 985-994
  • 21 Shapiro-Mendoza CK, Rice ME, Galang RR. et al. Pregnancy Outcomes After Maternal Zika Virus Infection During Pregnancy – U.S. Territories. MMWR Morb Mortal Wkly Rep 2017; 16: 615-621
  • 22 Johansson MA, Mier-y-Teran-Romero L, Reefhuis J. et al. Zika and the Risk of Microcephaly. N Engl J Med 2016; 375: 1-4
  • 23 Carvalho-Sauer R, Costa MDCN, Barreto FR. et al. Congenital Zika Syndrome: Prevalence of low birth weight and associated factors. Bahia, 2015–2017. Int J Infect Dis 2019; 82: 44-50
  • 24 Rick AM, Domek G, Cunningham M. et al. High Background Congenital Microcephaly in Rural Guatemala: Implications for Neonatal Congenital Zika Virus Infection Screening. Glob Health Sci Pract 2017; 5: 686-696
  • 25 Halai UA, Nielsen-Saines K, Moreira ML. et al. Maternal Zika Virus Disease Severity, Virus Load, Prior Dengue Antibodies, and Their Relationship to Birth Outcomes. Clin Infect Dis 2017; 65: 877-883