Prenatal circulating microRNA signatures of foetal Down syndrome.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
20 02 2019
Historique:
received: 08 01 2018
accepted: 02 10 2018
entrez: 22 2 2019
pubmed: 23 2 2019
medline: 15 9 2020
Statut: epublish

Résumé

The altered expression pattern of miRNAs might potentially reflect anomalies related to foetal chromosomal aberrations. The aim of the study was to determine the expression level of miRNAs in plasma of pregnant women with foetal Down syndrome (DS). Out of 198 amniocentesis performed at 15-18 weeks of gestation, within a group of 12 patients with foetal DS and 12 patients with uncomplicated pregnancies, who delivered healthy newborns at term, we examined the expression level of 800 miRNAs using the NanoString technology. Our study revealed that there are 6 miRNAs were upregulated (hsa-miR-15a, hsa-let-7d, hsa-miR-142, hsa-miR-23a, hsa-miR-199, hsa-miR-191) and 7 were downregulated (hsa-miR-1290, hsa-miR-1915, hsa-miR30e, hsa-miR-1260, hsa-miR-483, hsa-miR-548, hsa-miR-590) in plasma samples of women with foetal DS syndrome. The genes regulated by identified miRNAs are involved in central nervous system development, congenital abnormalities and heart defects. The results of the present study yielded information on DS-specific miRNA expression signature, which can further help to design a panel of miRNAs as a non-invasive test for DS diagnosis. We believe that identified miRNAs may attend in the pathogenesis of DS and would potentially make a significant role for the future preventive therapies.

Identifiants

pubmed: 30787377
doi: 10.1038/s41598-018-35876-5
pii: 10.1038/s41598-018-35876-5
pmc: PMC6382869
doi:

Substances chimiques

Biomarkers 0
Circulating MicroRNA 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2394

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Auteurs

Monika Zbucka-Kretowska (M)

Department of Reproduction and Gynaecological Endocrinology, Medical University of Bialystok, Bialystok, Poland. monikazbucka@wp.pl.

Magdalena Niemira (M)

Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.

Magdalena Paczkowska-Abdulsalam (M)

Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.

Agnieszka Bielska (A)

Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.

Anna Szalkowska (A)

Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.

Ewa Parfieniuk (E)

Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.

Michal Ciborowski (M)

Clinical Research Centre, Medical University of Bialystok, Bialystok, Poland.

Slawomir Wolczynski (S)

Department of Reproduction and Gynaecological Endocrinology, Medical University of Bialystok, Bialystok, Poland.

Adam Kretowski (A)

Clinical Research Centre; Department of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Bialystok, Poland.

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Classifications MeSH