Increased Circulating Levels of Tissue-Type Plasminogen Activator Are Associated with the Risk of Spontaneous Abortion During the First Trimester of Pregnancy.

early prediction extracellular vesicles prenatal care spontaneous abortion tissue plasminogen activator

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
01 Apr 2020
Historique:
received: 05 02 2020
revised: 05 03 2020
accepted: 11 03 2020
entrez: 5 4 2020
pubmed: 5 4 2020
medline: 5 4 2020
Statut: epublish

Résumé

Spontaneous abortion is a common complication in early pregnancy, with an incidence of around 20%. Ultrasound scan and measurement of human chorionic gonadotropin are used to identify patients at risk of spontaneous abortion; however, there is a clinical need to find new biomarkers to prospectively identify patients before the onset of clinical symptoms. Here, we aim to investigate potential biomarkers of spontaneous abortion taken in the first clinical appointment of pregnancy. A case-control study was conducted based on a prospectively collected cohort in which cases and controls were retrospectively stratified based on pregnancy outcome: normal healthy pregnancies (controls = 33) and pregnancies that ended in spontaneous abortion (cases = 10). We evaluated extracellular vesicles isolated by precipitation with ExoQuick™ and protein concentrations of tissue plasminogen activator, leptin, and adiponectin measured by ELISA. The extracellular vesicles showed the typical morphology and membrane proteins: CD63, Alix, and Flotilin-1. The size distributions of the isolated extracellular vesicles were 112 ± 27 and 118 ± 28 nm in diameter for controls and spontaneous abortion, respectively, and the total amount of extracellular vesicles did not show any difference between controls and the spontaneous abortion group. The tissue plasminogen activator showed a significant difference (

Identifiants

pubmed: 32244842
pii: diagnostics10040197
doi: 10.3390/diagnostics10040197
pmc: PMC7235768
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Lara J Monteiro (LJ)

Centre for Biomedical Research, Laboratory of Reproductive Biology, Faculty of Medicine, Universidad de Los Andes, Santiago 7620001, Chile.

Manuel Varas-Godoy (M)

Centre for Biomedical Research, Laboratory of Reproductive Biology, Faculty of Medicine, Universidad de Los Andes, Santiago 7620001, Chile.
Cancer Cell Biology Lab., Centre of Celullar Biology and Biomedicine (CEBICEM), Faculty of Medicine and Science, Universidad San Sebastián, Santiago 7510157, Chile.

Stephanie Acuña-Gallardo (S)

Centre for Biomedical Research, Laboratory of Reproductive Biology, Faculty of Medicine, Universidad de Los Andes, Santiago 7620001, Chile.

Paula Correa (P)

Department of Obstetrics and Gynecology, Faculty of Medicine, Universidad de los Andes, Santiago 7620001, Chile.
Department of Maternal-Fetal Medicine, Clínica Dávila, Santiago 8420384, Chile.

Gianluca Passalacqua (G)

Centre for Biomedical Research, Laboratory of Reproductive Biology, Faculty of Medicine, Universidad de Los Andes, Santiago 7620001, Chile.

Max Monckeberg (M)

Department of Obstetrics and Gynecology, Faculty of Medicine, Universidad de los Andes, Santiago 7620001, Chile.

Gregory E Rice (GE)

Centre for Biomedical Research, Laboratory of Reproductive Biology, Faculty of Medicine, Universidad de Los Andes, Santiago 7620001, Chile.
Centre for Clinical Research, University of Queensland, QLD 4029 Herston, Australia.

Sebastián E Illanes (SE)

Centre for Biomedical Research, Laboratory of Reproductive Biology, Faculty of Medicine, Universidad de Los Andes, Santiago 7620001, Chile.
Department of Obstetrics and Gynecology, Faculty of Medicine, Universidad de los Andes, Santiago 7620001, Chile.
Department of Maternal-Fetal Medicine, Clínica Dávila, Santiago 8420384, Chile.

Classifications MeSH