Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Laudanski, Piotr, Zbucka-Kretowska, Monika, Charkiewicz, Karol, Wolczynski, Slawomir, Wojcik, Daniela, Charkiewicz, Radoslaw
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
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
_version_ 1782346781942611968
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
work_keys_str_mv AT laudanskipiotr maternalplasmaandamnioticfluidchemokinesscreeninginfetaldownsyndrome
AT zbuckakretowskamonika maternalplasmaandamnioticfluidchemokinesscreeninginfetaldownsyndrome
AT charkiewiczkarol maternalplasmaandamnioticfluidchemokinesscreeninginfetaldownsyndrome
AT wolczynskislawomir maternalplasmaandamnioticfluidchemokinesscreeninginfetaldownsyndrome
AT wojcikdaniela maternalplasmaandamnioticfluidchemokinesscreeninginfetaldownsyndrome
AT charkiewiczradoslaw maternalplasmaandamnioticfluidchemokinesscreeninginfetaldownsyndrome