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The comparison of plasma fibronectin in term and preterm delivery: A cross-sectional, descriptive-analytical study
BACKGROUND: Preterm delivery is one of the main causes of infant death. Therefore, prediction of preterm delivery may eliminate a large number of prenatal complications. OBJECTIVE: The present study aimed to understand if preterm delivery can be predicted by assessing maternal plasma fibronectin con...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Knowledge E
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996127/ https://www.ncbi.nlm.nih.gov/pubmed/32043067 http://dx.doi.org/10.18502/ijrm.v18i1.6191 |
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author | Moradi, Zahra Moradi, Parvin Hassan Meshkibaf, Mohamad Aleosfoor, Mehrnoosh Sharafi, Mehdi Jafarzadeh, Saeedeh |
author_facet | Moradi, Zahra Moradi, Parvin Hassan Meshkibaf, Mohamad Aleosfoor, Mehrnoosh Sharafi, Mehdi Jafarzadeh, Saeedeh |
author_sort | Moradi, Zahra |
collection | PubMed |
description | BACKGROUND: Preterm delivery is one of the main causes of infant death. Therefore, prediction of preterm delivery may eliminate a large number of prenatal complications. OBJECTIVE: The present study aimed to understand if preterm delivery can be predicted by assessing maternal plasma fibronectin concentration. MATERIALS AND METHODS: Serum samples from 105 pregnant women participating in this study were collected. The plasma fibronectin were measured at 24-28 wk of gestation and again at 32-36 wk of gestation. Unfortunately, only 65 of the 105 pregnant women, returned for the second sampling. The plasma fibronectin was analyzed using ELISA method and its concentration in term and preterm deliveries was compared. The delivery dates of all the women were also recorded. RESULTS: Out of 105 pregnant women, 28 delivered preterm (26.7%). The Plasma fibronectin concentrations in women with preterm delivery were higher than in those who delivered at term (p = 0.001). Accordingly, Plasma fibronectin concentrations were significantly higher in the second serum samples (p = 0.01). Plasma fibronectin concentrations was also higher in obese women and in those suffering from preeclampsia (p = 0.12) and gestational diabetes (p = 0.81). CONCLUSION: Plasma fibronectin concentrations test could be used as an optional screening test for preterm delivery at 28 to 34 wk of gestation in pregnant women who prefer to avoid vaginal sampling. |
format | Online Article Text |
id | pubmed-6996127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Knowledge E |
record_format | MEDLINE/PubMed |
spelling | pubmed-69961272020-02-10 The comparison of plasma fibronectin in term and preterm delivery: A cross-sectional, descriptive-analytical study Moradi, Zahra Moradi, Parvin Hassan Meshkibaf, Mohamad Aleosfoor, Mehrnoosh Sharafi, Mehdi Jafarzadeh, Saeedeh Int J Reprod Biomed Research Article BACKGROUND: Preterm delivery is one of the main causes of infant death. Therefore, prediction of preterm delivery may eliminate a large number of prenatal complications. OBJECTIVE: The present study aimed to understand if preterm delivery can be predicted by assessing maternal plasma fibronectin concentration. MATERIALS AND METHODS: Serum samples from 105 pregnant women participating in this study were collected. The plasma fibronectin were measured at 24-28 wk of gestation and again at 32-36 wk of gestation. Unfortunately, only 65 of the 105 pregnant women, returned for the second sampling. The plasma fibronectin was analyzed using ELISA method and its concentration in term and preterm deliveries was compared. The delivery dates of all the women were also recorded. RESULTS: Out of 105 pregnant women, 28 delivered preterm (26.7%). The Plasma fibronectin concentrations in women with preterm delivery were higher than in those who delivered at term (p = 0.001). Accordingly, Plasma fibronectin concentrations were significantly higher in the second serum samples (p = 0.01). Plasma fibronectin concentrations was also higher in obese women and in those suffering from preeclampsia (p = 0.12) and gestational diabetes (p = 0.81). CONCLUSION: Plasma fibronectin concentrations test could be used as an optional screening test for preterm delivery at 28 to 34 wk of gestation in pregnant women who prefer to avoid vaginal sampling. Knowledge E 2020-01-27 /pmc/articles/PMC6996127/ /pubmed/32043067 http://dx.doi.org/10.18502/ijrm.v18i1.6191 Text en Copyright © 2020 Moradi et al. https://creativecommons.org/licenses/by/4.0/ 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. which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Article Moradi, Zahra Moradi, Parvin Hassan Meshkibaf, Mohamad Aleosfoor, Mehrnoosh Sharafi, Mehdi Jafarzadeh, Saeedeh The comparison of plasma fibronectin in term and preterm delivery: A cross-sectional, descriptive-analytical study |
title | The comparison of plasma fibronectin in term and preterm delivery: A cross-sectional, descriptive-analytical study |
title_full | The comparison of plasma fibronectin in term and preterm delivery: A cross-sectional, descriptive-analytical study |
title_fullStr | The comparison of plasma fibronectin in term and preterm delivery: A cross-sectional, descriptive-analytical study |
title_full_unstemmed | The comparison of plasma fibronectin in term and preterm delivery: A cross-sectional, descriptive-analytical study |
title_short | The comparison of plasma fibronectin in term and preterm delivery: A cross-sectional, descriptive-analytical study |
title_sort | comparison of plasma fibronectin in term and preterm delivery: a cross-sectional, descriptive-analytical study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996127/ https://www.ncbi.nlm.nih.gov/pubmed/32043067 http://dx.doi.org/10.18502/ijrm.v18i1.6191 |
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