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Prevalence of microcephaly and Zika virus infection in a pregnancy cohort in Kenya, 2017–2019
BACKGROUND: Zika virus (ZIKV), first discovered in Uganda in 1947, re-emerged globally in 2013 and was later associated with microcephaly and other birth defects. We determined the incidence of ZIKV infection and its association with adverse pregnancy and fetal outcomes in a pregnancy cohort in Keny...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470235/ https://www.ncbi.nlm.nih.gov/pubmed/36100910 http://dx.doi.org/10.1186/s12916-022-02498-8 |
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author | Osoro, Eric Inwani, Irene Mugo, Cyrus Hunsperger, Elizabeth Verani, Jennifer R. Omballa, Victor Wamalwa, Dalton Rhee, Chulwoo Nduati, Ruth Kinuthia, John Jin, Hafsa Okutoyi, Lydia Mwaengo, Dufton Maugo, Brian Otieno, Nancy A. Mirieri, Harriet Shabibi, Mufida Munyua, Peninah Njenga, M. Kariuki Widdowson, Marc-Alain |
author_facet | Osoro, Eric Inwani, Irene Mugo, Cyrus Hunsperger, Elizabeth Verani, Jennifer R. Omballa, Victor Wamalwa, Dalton Rhee, Chulwoo Nduati, Ruth Kinuthia, John Jin, Hafsa Okutoyi, Lydia Mwaengo, Dufton Maugo, Brian Otieno, Nancy A. Mirieri, Harriet Shabibi, Mufida Munyua, Peninah Njenga, M. Kariuki Widdowson, Marc-Alain |
author_sort | Osoro, Eric |
collection | PubMed |
description | BACKGROUND: Zika virus (ZIKV), first discovered in Uganda in 1947, re-emerged globally in 2013 and was later associated with microcephaly and other birth defects. We determined the incidence of ZIKV infection and its association with adverse pregnancy and fetal outcomes in a pregnancy cohort in Kenya. METHODS: From October 2017 to July 2019, we recruited and followed up women aged ≥ 15 years and ≤ 28 weeks pregnant in three hospitals in coastal Mombasa. Monthly follow-up included risk factor questions and a blood sample collected for ZIKV serology. We collected anthropometric measures (including head circumference), cord blood, venous blood from newborns, and any evidence of birth defects. Microcephaly was defined as a head circumference (HC) < 2 standard deviations (SD) for sex and gestational age. Severe microcephaly was defined as HC < 3 SD for sex and age. We tested sera for anti-ZIKV IgM antibodies using capture enzyme-linked immunosorbent assay (ELISA) and confirmed positives using the plaque reduction neutralization test (PRNT(90)) for ZIKV and for dengue (DENV) on the samples that were ZIKV neutralizing antibody positive. We collected blood and urine from participants reporting fever or rash for ZIKV testing. RESULTS: Of 2889 pregnant women screened for eligibility, 2312 (80%) were enrolled. Of 1916 recorded deliveries, 1816 (94.6%) were live births and 100 (5.2%) were either stillbirths or spontaneous abortions (< 22 weeks of gestation). Among 1236 newborns with complete anthropometric measures, 11 (0.9%) had microcephaly and 3 (0.2%) had severe microcephaly. A total of 166 (7.2%) participants were positive for anti-ZIKV IgM, 136 of whom became seropositive during follow-up. Among the 166 anti-ZIKV IgM positive, 3 and 18 participants were further seropositive for ZIKV and DENV neutralizing antibodies, respectively. Of these 3 and 18 pregnant women, one and 13 (72.2%) seroconverted with antibodies to ZIKV and DENV, respectively. All 308 samples (serum and urine samples collected during sick visits and samples that were anti-ZIKV IgM positive) tested by RT-PCR were negative for ZIKV. No adverse pregnancy or neonatal outcomes were reported among the three participants with confirmed ZIKV exposure. Among newborns from pregnant women with DENV exposure, four (22.2%) were small for gestational age and one (5.6%) had microcephaly. CONCLUSIONS: The prevalence of severe microcephaly among newborns in coastal Kenya was high relative to published estimates from facility-based studies in Europe and Latin America, but little evidence of ZIKV transmission. There is a need for improved surveillance for microcephaly and other congenital malformations in Kenya. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02498-8. |
format | Online Article Text |
id | pubmed-9470235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-94702352022-09-14 Prevalence of microcephaly and Zika virus infection in a pregnancy cohort in Kenya, 2017–2019 Osoro, Eric Inwani, Irene Mugo, Cyrus Hunsperger, Elizabeth Verani, Jennifer R. Omballa, Victor Wamalwa, Dalton Rhee, Chulwoo Nduati, Ruth Kinuthia, John Jin, Hafsa Okutoyi, Lydia Mwaengo, Dufton Maugo, Brian Otieno, Nancy A. Mirieri, Harriet Shabibi, Mufida Munyua, Peninah Njenga, M. Kariuki Widdowson, Marc-Alain BMC Med Research Article BACKGROUND: Zika virus (ZIKV), first discovered in Uganda in 1947, re-emerged globally in 2013 and was later associated with microcephaly and other birth defects. We determined the incidence of ZIKV infection and its association with adverse pregnancy and fetal outcomes in a pregnancy cohort in Kenya. METHODS: From October 2017 to July 2019, we recruited and followed up women aged ≥ 15 years and ≤ 28 weeks pregnant in three hospitals in coastal Mombasa. Monthly follow-up included risk factor questions and a blood sample collected for ZIKV serology. We collected anthropometric measures (including head circumference), cord blood, venous blood from newborns, and any evidence of birth defects. Microcephaly was defined as a head circumference (HC) < 2 standard deviations (SD) for sex and gestational age. Severe microcephaly was defined as HC < 3 SD for sex and age. We tested sera for anti-ZIKV IgM antibodies using capture enzyme-linked immunosorbent assay (ELISA) and confirmed positives using the plaque reduction neutralization test (PRNT(90)) for ZIKV and for dengue (DENV) on the samples that were ZIKV neutralizing antibody positive. We collected blood and urine from participants reporting fever or rash for ZIKV testing. RESULTS: Of 2889 pregnant women screened for eligibility, 2312 (80%) were enrolled. Of 1916 recorded deliveries, 1816 (94.6%) were live births and 100 (5.2%) were either stillbirths or spontaneous abortions (< 22 weeks of gestation). Among 1236 newborns with complete anthropometric measures, 11 (0.9%) had microcephaly and 3 (0.2%) had severe microcephaly. A total of 166 (7.2%) participants were positive for anti-ZIKV IgM, 136 of whom became seropositive during follow-up. Among the 166 anti-ZIKV IgM positive, 3 and 18 participants were further seropositive for ZIKV and DENV neutralizing antibodies, respectively. Of these 3 and 18 pregnant women, one and 13 (72.2%) seroconverted with antibodies to ZIKV and DENV, respectively. All 308 samples (serum and urine samples collected during sick visits and samples that were anti-ZIKV IgM positive) tested by RT-PCR were negative for ZIKV. No adverse pregnancy or neonatal outcomes were reported among the three participants with confirmed ZIKV exposure. Among newborns from pregnant women with DENV exposure, four (22.2%) were small for gestational age and one (5.6%) had microcephaly. CONCLUSIONS: The prevalence of severe microcephaly among newborns in coastal Kenya was high relative to published estimates from facility-based studies in Europe and Latin America, but little evidence of ZIKV transmission. There is a need for improved surveillance for microcephaly and other congenital malformations in Kenya. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02498-8. BioMed Central 2022-09-14 /pmc/articles/PMC9470235/ /pubmed/36100910 http://dx.doi.org/10.1186/s12916-022-02498-8 Text en © The Author(s) 2022 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 | Research Article Osoro, Eric Inwani, Irene Mugo, Cyrus Hunsperger, Elizabeth Verani, Jennifer R. Omballa, Victor Wamalwa, Dalton Rhee, Chulwoo Nduati, Ruth Kinuthia, John Jin, Hafsa Okutoyi, Lydia Mwaengo, Dufton Maugo, Brian Otieno, Nancy A. Mirieri, Harriet Shabibi, Mufida Munyua, Peninah Njenga, M. Kariuki Widdowson, Marc-Alain Prevalence of microcephaly and Zika virus infection in a pregnancy cohort in Kenya, 2017–2019 |
title | Prevalence of microcephaly and Zika virus infection in a pregnancy cohort in Kenya, 2017–2019 |
title_full | Prevalence of microcephaly and Zika virus infection in a pregnancy cohort in Kenya, 2017–2019 |
title_fullStr | Prevalence of microcephaly and Zika virus infection in a pregnancy cohort in Kenya, 2017–2019 |
title_full_unstemmed | Prevalence of microcephaly and Zika virus infection in a pregnancy cohort in Kenya, 2017–2019 |
title_short | Prevalence of microcephaly and Zika virus infection in a pregnancy cohort in Kenya, 2017–2019 |
title_sort | prevalence of microcephaly and zika virus infection in a pregnancy cohort in kenya, 2017–2019 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470235/ https://www.ncbi.nlm.nih.gov/pubmed/36100910 http://dx.doi.org/10.1186/s12916-022-02498-8 |
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