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Maternal Plasma and Amniotic Fluid Chemokines Screening in Fetal Down Syndrome
Objective. Chemokines exert different inflammatory responses which can potentially be related to certain fetal chromosomal abnormalities. The aim of the study was to determine the concentration of selected chemokines in plasma and amniotic fluid of women with fetal Down syndrome. Method. Out of 171...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248337/ https://www.ncbi.nlm.nih.gov/pubmed/25477715 http://dx.doi.org/10.1155/2014/835837 |
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author | Laudanski, Piotr Zbucka-Kretowska, Monika Charkiewicz, Karol Wolczynski, Slawomir Wojcik, Daniela Charkiewicz, Radoslaw |
author_facet | Laudanski, Piotr Zbucka-Kretowska, Monika Charkiewicz, Karol Wolczynski, Slawomir Wojcik, Daniela Charkiewicz, Radoslaw |
author_sort | Laudanski, Piotr |
collection | PubMed |
description | Objective. Chemokines exert different inflammatory responses which can potentially be related to certain fetal chromosomal abnormalities. The aim of the study was to determine the concentration of selected chemokines in plasma and amniotic fluid of women with fetal Down syndrome. Method. Out of 171 amniocentesis, we had 7 patients with confirmed fetal Down syndrome (15th–18th weeks of gestation). For the purpose of our control, we chose 14 women without confirmed chromosomal aberration. To assess the concentration of chemokines in the blood plasma and amniotic fluid, we used a protein macroarray, which allows the simultaneous determination of 40 chemokines per sample. Results. We showed significant decrease in the concentration of 4 chemokines, HCC-4, IL-28A, IL-31, and MCP-2, and increase in the concentration of CXCL7 (NAP-2) in plasma of women with fetal Down syndrome. Furthermore, we showed decrease in concentration of 3 chemokines, ITAC, MCP-3, MIF, and increase in concentration of 4 chemokines, IP-10, MPIF-1, CXCL7, and 6Ckine, in amniotic fluid of women with fetal Down syndrome. Conclusion. On the basis of our findings, our hypothesis is that the chemokines may play role in the pathogenesis of Down syndrome. Defining their potential as biochemical markers of Down syndrome requires further investigation on larger group of patients. |
format | Online Article Text |
id | pubmed-4248337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42483372014-12-04 Maternal Plasma and Amniotic Fluid Chemokines Screening in Fetal Down Syndrome Laudanski, Piotr Zbucka-Kretowska, Monika Charkiewicz, Karol Wolczynski, Slawomir Wojcik, Daniela Charkiewicz, Radoslaw Mediators Inflamm Research Article Objective. Chemokines exert different inflammatory responses which can potentially be related to certain fetal chromosomal abnormalities. The aim of the study was to determine the concentration of selected chemokines in plasma and amniotic fluid of women with fetal Down syndrome. Method. Out of 171 amniocentesis, we had 7 patients with confirmed fetal Down syndrome (15th–18th weeks of gestation). For the purpose of our control, we chose 14 women without confirmed chromosomal aberration. To assess the concentration of chemokines in the blood plasma and amniotic fluid, we used a protein macroarray, which allows the simultaneous determination of 40 chemokines per sample. Results. We showed significant decrease in the concentration of 4 chemokines, HCC-4, IL-28A, IL-31, and MCP-2, and increase in the concentration of CXCL7 (NAP-2) in plasma of women with fetal Down syndrome. Furthermore, we showed decrease in concentration of 3 chemokines, ITAC, MCP-3, MIF, and increase in concentration of 4 chemokines, IP-10, MPIF-1, CXCL7, and 6Ckine, in amniotic fluid of women with fetal Down syndrome. Conclusion. On the basis of our findings, our hypothesis is that the chemokines may play role in the pathogenesis of Down syndrome. Defining their potential as biochemical markers of Down syndrome requires further investigation on larger group of patients. Hindawi Publishing Corporation 2014 2014-11-16 /pmc/articles/PMC4248337/ /pubmed/25477715 http://dx.doi.org/10.1155/2014/835837 Text en Copyright © 2014 Piotr Laudanski et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Laudanski, Piotr Zbucka-Kretowska, Monika Charkiewicz, Karol Wolczynski, Slawomir Wojcik, Daniela Charkiewicz, Radoslaw Maternal Plasma and Amniotic Fluid Chemokines Screening in Fetal Down Syndrome |
title | Maternal Plasma and Amniotic Fluid Chemokines Screening in Fetal Down Syndrome |
title_full | Maternal Plasma and Amniotic Fluid Chemokines Screening in Fetal Down Syndrome |
title_fullStr | Maternal Plasma and Amniotic Fluid Chemokines Screening in Fetal Down Syndrome |
title_full_unstemmed | Maternal Plasma and Amniotic Fluid Chemokines Screening in Fetal Down Syndrome |
title_short | Maternal Plasma and Amniotic Fluid Chemokines Screening in Fetal Down Syndrome |
title_sort | maternal plasma and amniotic fluid chemokines screening in fetal down syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248337/ https://www.ncbi.nlm.nih.gov/pubmed/25477715 http://dx.doi.org/10.1155/2014/835837 |
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