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Protein Concentrations of Thrombospondin-1, MIP-1β, and S100A8 Suggest the Reflection of a Pregnancy Clock in Mid-Trimester Amniotic Fluid

The development of immunoassays enables more sophisticated studies of the associations between protein concentrations and pregnancy outcomes, allowing early biomarker identification that can improve neonatal outcomes. The aim of this study was to explore associations between selected mid-trimester a...

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Autores principales: Viklund, Felicia, Hallingström, Maria, Kacerovsky, Marian, Cobo, Teresa, Skogstrand, Kristin, Hougaard, David M., Sävman, Karin, Carlsson, Ylva, Tsiartas, Panagiotis, Juodakis, Julius, Nilsson, Staffan, Jacobsson, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593301/
https://www.ncbi.nlm.nih.gov/pubmed/33026626
http://dx.doi.org/10.1007/s43032-020-00229-z
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author Viklund, Felicia
Hallingström, Maria
Kacerovsky, Marian
Cobo, Teresa
Skogstrand, Kristin
Hougaard, David M.
Sävman, Karin
Carlsson, Ylva
Tsiartas, Panagiotis
Juodakis, Julius
Nilsson, Staffan
Jacobsson, Bo
author_facet Viklund, Felicia
Hallingström, Maria
Kacerovsky, Marian
Cobo, Teresa
Skogstrand, Kristin
Hougaard, David M.
Sävman, Karin
Carlsson, Ylva
Tsiartas, Panagiotis
Juodakis, Julius
Nilsson, Staffan
Jacobsson, Bo
author_sort Viklund, Felicia
collection PubMed
description The development of immunoassays enables more sophisticated studies of the associations between protein concentrations and pregnancy outcomes, allowing early biomarker identification that can improve neonatal outcomes. The aim of this study was to explore associations between selected mid-trimester amniotic fluid proteins and (1) overall gestational duration and (2) spontaneous preterm delivery. A prospective cohort study, including women undergoing mid-trimester transabdominal genetic amniocentesis, was performed in Gothenburg, Sweden, 2008–2016 (n = 1072). A panel of 27 proteins related to inflammation was analyzed using Meso-Scale multiplex technology. Concentrations were adjusted for gestational age at sampling, experimental factors, year of sampling, and covariates (maternal age at sampling, parity (nulliparous/multiparous), smoking at first prenatal visit, and in vitro fertilization). Cox regression analysis of the entire cohort was performed to explore possible associations between protein concentrations and gestational duration. This was followed by Cox regression analysis censored at 259 days or longer, to investigate whether associations were detectable in women with spontaneous preterm delivery (n = 47). Finally, linear regression models were performed to analyze associations between protein concentrations and gestational duration in women with spontaneous onset of labor at term (n = 784). HMG-1, IGFBP-1, IL-18, MIP-1α, MIP-1β, S100A8, and thrombospondin-1 were significantly associated with gestational duration at term, but not preterm. Increased concentrations of thrombospondin-1, MIP-1β, and S100A8, respectively, were significantly associated with decreased gestational duration after the Holm-Bonferroni correction in women with spontaneous onset of labor at term. This adds to the concept of a pregnancy clock, where our findings suggest that such a clock is also reflected in the amniotic fluid at early mid-trimester, but further research is needed to confirm this.
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spelling pubmed-75933012020-11-10 Protein Concentrations of Thrombospondin-1, MIP-1β, and S100A8 Suggest the Reflection of a Pregnancy Clock in Mid-Trimester Amniotic Fluid Viklund, Felicia Hallingström, Maria Kacerovsky, Marian Cobo, Teresa Skogstrand, Kristin Hougaard, David M. Sävman, Karin Carlsson, Ylva Tsiartas, Panagiotis Juodakis, Julius Nilsson, Staffan Jacobsson, Bo Reprod Sci Original Article The development of immunoassays enables more sophisticated studies of the associations between protein concentrations and pregnancy outcomes, allowing early biomarker identification that can improve neonatal outcomes. The aim of this study was to explore associations between selected mid-trimester amniotic fluid proteins and (1) overall gestational duration and (2) spontaneous preterm delivery. A prospective cohort study, including women undergoing mid-trimester transabdominal genetic amniocentesis, was performed in Gothenburg, Sweden, 2008–2016 (n = 1072). A panel of 27 proteins related to inflammation was analyzed using Meso-Scale multiplex technology. Concentrations were adjusted for gestational age at sampling, experimental factors, year of sampling, and covariates (maternal age at sampling, parity (nulliparous/multiparous), smoking at first prenatal visit, and in vitro fertilization). Cox regression analysis of the entire cohort was performed to explore possible associations between protein concentrations and gestational duration. This was followed by Cox regression analysis censored at 259 days or longer, to investigate whether associations were detectable in women with spontaneous preterm delivery (n = 47). Finally, linear regression models were performed to analyze associations between protein concentrations and gestational duration in women with spontaneous onset of labor at term (n = 784). HMG-1, IGFBP-1, IL-18, MIP-1α, MIP-1β, S100A8, and thrombospondin-1 were significantly associated with gestational duration at term, but not preterm. Increased concentrations of thrombospondin-1, MIP-1β, and S100A8, respectively, were significantly associated with decreased gestational duration after the Holm-Bonferroni correction in women with spontaneous onset of labor at term. This adds to the concept of a pregnancy clock, where our findings suggest that such a clock is also reflected in the amniotic fluid at early mid-trimester, but further research is needed to confirm this. Springer International Publishing 2020-10-07 /pmc/articles/PMC7593301/ /pubmed/33026626 http://dx.doi.org/10.1007/s43032-020-00229-z Text en © The Author(s) 2020 Open Access This 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/.
spellingShingle Original Article
Viklund, Felicia
Hallingström, Maria
Kacerovsky, Marian
Cobo, Teresa
Skogstrand, Kristin
Hougaard, David M.
Sävman, Karin
Carlsson, Ylva
Tsiartas, Panagiotis
Juodakis, Julius
Nilsson, Staffan
Jacobsson, Bo
Protein Concentrations of Thrombospondin-1, MIP-1β, and S100A8 Suggest the Reflection of a Pregnancy Clock in Mid-Trimester Amniotic Fluid
title Protein Concentrations of Thrombospondin-1, MIP-1β, and S100A8 Suggest the Reflection of a Pregnancy Clock in Mid-Trimester Amniotic Fluid
title_full Protein Concentrations of Thrombospondin-1, MIP-1β, and S100A8 Suggest the Reflection of a Pregnancy Clock in Mid-Trimester Amniotic Fluid
title_fullStr Protein Concentrations of Thrombospondin-1, MIP-1β, and S100A8 Suggest the Reflection of a Pregnancy Clock in Mid-Trimester Amniotic Fluid
title_full_unstemmed Protein Concentrations of Thrombospondin-1, MIP-1β, and S100A8 Suggest the Reflection of a Pregnancy Clock in Mid-Trimester Amniotic Fluid
title_short Protein Concentrations of Thrombospondin-1, MIP-1β, and S100A8 Suggest the Reflection of a Pregnancy Clock in Mid-Trimester Amniotic Fluid
title_sort protein concentrations of thrombospondin-1, mip-1β, and s100a8 suggest the reflection of a pregnancy clock in mid-trimester amniotic fluid
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593301/
https://www.ncbi.nlm.nih.gov/pubmed/33026626
http://dx.doi.org/10.1007/s43032-020-00229-z
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