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The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates

Our aim was to investigate whether SARS-CoV-2 infection raised high risks of late pregnancy complications, and posed health problems in fetuses and neonates. We analyzed the data of COVID-19 pregnant women with COVID-19 during late pregnancy and their neonates. Eleven out of 16 (69%) pregnant women...

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Autores principales: Zhou, Jingjiao, Wang, Yudie, Zhao, Juan, Gu, Lixing, Yang, Cheng, Wang, Jun, Zhang, Heng, Tian, Yu, Tuo, Hu, Li, Dan, Wei, Min, He, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530551/
https://www.ncbi.nlm.nih.gov/pubmed/33006691
http://dx.doi.org/10.1007/s10096-020-04033-0
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author Zhou, Jingjiao
Wang, Yudie
Zhao, Juan
Gu, Lixing
Yang, Cheng
Wang, Jun
Zhang, Heng
Tian, Yu
Tuo, Hu
Li, Dan
Wei, Min
He, Bing
author_facet Zhou, Jingjiao
Wang, Yudie
Zhao, Juan
Gu, Lixing
Yang, Cheng
Wang, Jun
Zhang, Heng
Tian, Yu
Tuo, Hu
Li, Dan
Wei, Min
He, Bing
author_sort Zhou, Jingjiao
collection PubMed
description Our aim was to investigate whether SARS-CoV-2 infection raised high risks of late pregnancy complications, and posed health problems in fetuses and neonates. We analyzed the data of COVID-19 pregnant women with COVID-19 during late pregnancy and their neonates. Eleven out of 16 (69%) pregnant women with COVID-19 had ++ or +++ of ketone body in urine. The blood uric acid of pregnant patients was 334 μmol/L (IQR, 269–452). D-dimer and FDP in pregnant patients were 3.32 mg/L (IQR, 2.18–4.21) and 9.6 mg/L (IQR, 5.9–12.4). Results of blood samples collected at birth showed that 16 neonates had leukocytes (15.7 × 10(9)/L (IQR, 13.7–17.2)), neutrophils (11.1 × 10(9)/L (IQR, 9.2–13.2)), CK (401 U/L (IQR, 382–647)), and LDH (445 U/L (IQR, 417–559)). Twenty-four hours after birth, a neonate from COVID-19 woman had fever and positive of SARS-CoV-2 gene. Another woman had strongly positive for SARS-CoV-2 gene (+++) for 4 weeks, and delivered one neonate who had SARS-CoV-2 IgM (46 AU/mL) and IgG (140 AU/mL) on day 1 after birth. In the third trimester, COVID-19 infection in pregnant patients raised high risks of ketonuria, hypercoagulable state, and hyperfibrinolysis, which may lead to severe complications. COVID-19 increased the inflammatory responses of placenta, and fetuses and neonates had potential organ dysregulation and coagulation disorders. There was a potential intrauterine transmission while pregnant women had high titer of SARS-CoV-2, but it is necessary to detect SARS-CoV-2 in the blood cord, placenta, and amniotic fluid to further confirm intrauterine infection of fetuses.
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spelling pubmed-75305512020-10-02 The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates Zhou, Jingjiao Wang, Yudie Zhao, Juan Gu, Lixing Yang, Cheng Wang, Jun Zhang, Heng Tian, Yu Tuo, Hu Li, Dan Wei, Min He, Bing Eur J Clin Microbiol Infect Dis Original Article Our aim was to investigate whether SARS-CoV-2 infection raised high risks of late pregnancy complications, and posed health problems in fetuses and neonates. We analyzed the data of COVID-19 pregnant women with COVID-19 during late pregnancy and their neonates. Eleven out of 16 (69%) pregnant women with COVID-19 had ++ or +++ of ketone body in urine. The blood uric acid of pregnant patients was 334 μmol/L (IQR, 269–452). D-dimer and FDP in pregnant patients were 3.32 mg/L (IQR, 2.18–4.21) and 9.6 mg/L (IQR, 5.9–12.4). Results of blood samples collected at birth showed that 16 neonates had leukocytes (15.7 × 10(9)/L (IQR, 13.7–17.2)), neutrophils (11.1 × 10(9)/L (IQR, 9.2–13.2)), CK (401 U/L (IQR, 382–647)), and LDH (445 U/L (IQR, 417–559)). Twenty-four hours after birth, a neonate from COVID-19 woman had fever and positive of SARS-CoV-2 gene. Another woman had strongly positive for SARS-CoV-2 gene (+++) for 4 weeks, and delivered one neonate who had SARS-CoV-2 IgM (46 AU/mL) and IgG (140 AU/mL) on day 1 after birth. In the third trimester, COVID-19 infection in pregnant patients raised high risks of ketonuria, hypercoagulable state, and hyperfibrinolysis, which may lead to severe complications. COVID-19 increased the inflammatory responses of placenta, and fetuses and neonates had potential organ dysregulation and coagulation disorders. There was a potential intrauterine transmission while pregnant women had high titer of SARS-CoV-2, but it is necessary to detect SARS-CoV-2 in the blood cord, placenta, and amniotic fluid to further confirm intrauterine infection of fetuses. Springer Berlin Heidelberg 2020-10-02 2021 /pmc/articles/PMC7530551/ /pubmed/33006691 http://dx.doi.org/10.1007/s10096-020-04033-0 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Zhou, Jingjiao
Wang, Yudie
Zhao, Juan
Gu, Lixing
Yang, Cheng
Wang, Jun
Zhang, Heng
Tian, Yu
Tuo, Hu
Li, Dan
Wei, Min
He, Bing
The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates
title The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates
title_full The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates
title_fullStr The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates
title_full_unstemmed The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates
title_short The metabolic and immunological characteristics of pregnant women with COVID-19 and their neonates
title_sort metabolic and immunological characteristics of pregnant women with covid-19 and their neonates
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530551/
https://www.ncbi.nlm.nih.gov/pubmed/33006691
http://dx.doi.org/10.1007/s10096-020-04033-0
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