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Lack of Association between Adverse Pregnancy Outcomes and Zika Antibodies among Pregnant Women in Thailand between 1997 and 2015

Data about Zika virus infection and adverse pregnancy outcomes in Southeast Asia are scarce. We conducted an unmatched case-control study of Zika virus (ZIKV) serology in pregnant women enrolled in human immunodeficiency virus (HIV) or hepatitis B virus (HBV) perinatal prevention trials between 1997...

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Autores principales: Ngo-Giang-Huong, Nicole, Leroi, Charline, Fusco, Dahlene, Cressey, Tim R., Wangsaeng, Nantawan, Salvadori, Nicolas, Kongyai, Natedao, Sirirungsi, Wasna, Lallemant, Marc, Auewarakul, Prasert, Khamduang, Woottichai, Jourdain, Gonzague
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402824/
https://www.ncbi.nlm.nih.gov/pubmed/34452289
http://dx.doi.org/10.3390/v13081423
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author Ngo-Giang-Huong, Nicole
Leroi, Charline
Fusco, Dahlene
Cressey, Tim R.
Wangsaeng, Nantawan
Salvadori, Nicolas
Kongyai, Natedao
Sirirungsi, Wasna
Lallemant, Marc
Auewarakul, Prasert
Khamduang, Woottichai
Jourdain, Gonzague
author_facet Ngo-Giang-Huong, Nicole
Leroi, Charline
Fusco, Dahlene
Cressey, Tim R.
Wangsaeng, Nantawan
Salvadori, Nicolas
Kongyai, Natedao
Sirirungsi, Wasna
Lallemant, Marc
Auewarakul, Prasert
Khamduang, Woottichai
Jourdain, Gonzague
author_sort Ngo-Giang-Huong, Nicole
collection PubMed
description Data about Zika virus infection and adverse pregnancy outcomes in Southeast Asia are scarce. We conducted an unmatched case-control study of Zika virus (ZIKV) serology in pregnant women enrolled in human immunodeficiency virus (HIV) or hepatitis B virus (HBV) perinatal prevention trials between 1997 and 2015 in Thailand. Case and control groups included women with and without adverse pregnancy outcomes. Plasma samples collected during the last trimester of pregnancy were tested for ZIKV IgG/IgM and Dengue IgG/IgM (Euroimmun, AG, Germany). Case newborn plasma samples were tested for ZIKV IgM and ZIKV RNA (Viasure, Spain). The case group included women with stillbirth (n = 22) or whose infants had microcephaly (n = 4), a head circumference below the first percentile (n = 14), neurological disorders (n = 36), or had died within 10 days after birth (n = 11). No women in the case group were positive for ZIKV IgM, and none of their live-born neonates were positive for ZIKV IgM or ZIKV RNA. The overall ZIKV IgG prevalence was 29%, 24% in the case and 34% in the control groups (Fisher’s exact test; p = 0.13), while the dengue IgG seroprevalence was 90%. Neither neonatal ZIKV infections nor ZIKV-related adverse pregnancy outcomes were observed in these women with HIV and/or HBV during the 18-year study period.
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spelling pubmed-84028242021-08-29 Lack of Association between Adverse Pregnancy Outcomes and Zika Antibodies among Pregnant Women in Thailand between 1997 and 2015 Ngo-Giang-Huong, Nicole Leroi, Charline Fusco, Dahlene Cressey, Tim R. Wangsaeng, Nantawan Salvadori, Nicolas Kongyai, Natedao Sirirungsi, Wasna Lallemant, Marc Auewarakul, Prasert Khamduang, Woottichai Jourdain, Gonzague Viruses Article Data about Zika virus infection and adverse pregnancy outcomes in Southeast Asia are scarce. We conducted an unmatched case-control study of Zika virus (ZIKV) serology in pregnant women enrolled in human immunodeficiency virus (HIV) or hepatitis B virus (HBV) perinatal prevention trials between 1997 and 2015 in Thailand. Case and control groups included women with and without adverse pregnancy outcomes. Plasma samples collected during the last trimester of pregnancy were tested for ZIKV IgG/IgM and Dengue IgG/IgM (Euroimmun, AG, Germany). Case newborn plasma samples were tested for ZIKV IgM and ZIKV RNA (Viasure, Spain). The case group included women with stillbirth (n = 22) or whose infants had microcephaly (n = 4), a head circumference below the first percentile (n = 14), neurological disorders (n = 36), or had died within 10 days after birth (n = 11). No women in the case group were positive for ZIKV IgM, and none of their live-born neonates were positive for ZIKV IgM or ZIKV RNA. The overall ZIKV IgG prevalence was 29%, 24% in the case and 34% in the control groups (Fisher’s exact test; p = 0.13), while the dengue IgG seroprevalence was 90%. Neither neonatal ZIKV infections nor ZIKV-related adverse pregnancy outcomes were observed in these women with HIV and/or HBV during the 18-year study period. MDPI 2021-07-22 /pmc/articles/PMC8402824/ /pubmed/34452289 http://dx.doi.org/10.3390/v13081423 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ngo-Giang-Huong, Nicole
Leroi, Charline
Fusco, Dahlene
Cressey, Tim R.
Wangsaeng, Nantawan
Salvadori, Nicolas
Kongyai, Natedao
Sirirungsi, Wasna
Lallemant, Marc
Auewarakul, Prasert
Khamduang, Woottichai
Jourdain, Gonzague
Lack of Association between Adverse Pregnancy Outcomes and Zika Antibodies among Pregnant Women in Thailand between 1997 and 2015
title Lack of Association between Adverse Pregnancy Outcomes and Zika Antibodies among Pregnant Women in Thailand between 1997 and 2015
title_full Lack of Association between Adverse Pregnancy Outcomes and Zika Antibodies among Pregnant Women in Thailand between 1997 and 2015
title_fullStr Lack of Association between Adverse Pregnancy Outcomes and Zika Antibodies among Pregnant Women in Thailand between 1997 and 2015
title_full_unstemmed Lack of Association between Adverse Pregnancy Outcomes and Zika Antibodies among Pregnant Women in Thailand between 1997 and 2015
title_short Lack of Association between Adverse Pregnancy Outcomes and Zika Antibodies among Pregnant Women in Thailand between 1997 and 2015
title_sort lack of association between adverse pregnancy outcomes and zika antibodies among pregnant women in thailand between 1997 and 2015
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402824/
https://www.ncbi.nlm.nih.gov/pubmed/34452289
http://dx.doi.org/10.3390/v13081423
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