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MicroRNA‐132 is overexpressed in fetuses with late‐onset fetal growth restriction

BACKGROUND AND AIMS: To evaluate the expression of microRNA 132 (miR‐132) in fetuses with normal growth and in fetuses with late‐onset growth restriction (FGR). METHODS: In a prospective cohort study, 48 fetuses (24 with late‐onset FGR and 24 with normal growth) were scanned with Doppler ultrasound...

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Autores principales: Morales‐Roselló, José, Loscalzo, Gabriela, García‐Lopez, Eva María, García‐Gimenez, José Luis, Perales‐Marín, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8922531/
https://www.ncbi.nlm.nih.gov/pubmed/35317418
http://dx.doi.org/10.1002/hsr2.558
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author Morales‐Roselló, José
Loscalzo, Gabriela
García‐Lopez, Eva María
García‐Gimenez, José Luis
Perales‐Marín, Alfredo
author_facet Morales‐Roselló, José
Loscalzo, Gabriela
García‐Lopez, Eva María
García‐Gimenez, José Luis
Perales‐Marín, Alfredo
author_sort Morales‐Roselló, José
collection PubMed
description BACKGROUND AND AIMS: To evaluate the expression of microRNA 132 (miR‐132) in fetuses with normal growth and in fetuses with late‐onset growth restriction (FGR). METHODS: In a prospective cohort study, 48 fetuses (24 with late‐onset FGR and 24 with normal growth) were scanned with Doppler ultrasound after 34 weeks to measure the umbilical artery and middle cerebral artery pulsatility indices and followed until birth. Subsequently, blood samples from the umbilical cord were collected to evaluate the expression of miR‐132 by means of Real‐time quantitative polymerase chain reaction, determining the existence of normality cut‐offs and associations with birth weight (BW) centile, cerebroplacental ratio multiples of the median (CPR MoM), and intrapartum fetal compromise (IFC). RESULTS: In comparison with normal fetuses, late‐onset FGR fetuses showed upregulation of miR‐132 (33.94 ± 45.04 vs. 2.88 ± 9.32 2−ddC (t), p < 0.001). Using 5 as a cut‐off we obtained a sensitivity of 50% and a specificity of 96% for the diagnosis of FGR, while for IFC these values were respectively 27% and 73%. Expression of miR‐132 was associated with BW centile but not with CPR MoM. Finally, the best detection of IFC was achieved combining miR‐132 expression and CPR MoM (AUC = 0.69, p < 0.05). CONCLUSION: Fetuses with late‐onset FGR show upregulation of miR‐132. Further studies are needed to investigate the role of miR‐132 in the management of late‐onset FGR.
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spelling pubmed-89225312022-03-21 MicroRNA‐132 is overexpressed in fetuses with late‐onset fetal growth restriction Morales‐Roselló, José Loscalzo, Gabriela García‐Lopez, Eva María García‐Gimenez, José Luis Perales‐Marín, Alfredo Health Sci Rep Original Research BACKGROUND AND AIMS: To evaluate the expression of microRNA 132 (miR‐132) in fetuses with normal growth and in fetuses with late‐onset growth restriction (FGR). METHODS: In a prospective cohort study, 48 fetuses (24 with late‐onset FGR and 24 with normal growth) were scanned with Doppler ultrasound after 34 weeks to measure the umbilical artery and middle cerebral artery pulsatility indices and followed until birth. Subsequently, blood samples from the umbilical cord were collected to evaluate the expression of miR‐132 by means of Real‐time quantitative polymerase chain reaction, determining the existence of normality cut‐offs and associations with birth weight (BW) centile, cerebroplacental ratio multiples of the median (CPR MoM), and intrapartum fetal compromise (IFC). RESULTS: In comparison with normal fetuses, late‐onset FGR fetuses showed upregulation of miR‐132 (33.94 ± 45.04 vs. 2.88 ± 9.32 2−ddC (t), p < 0.001). Using 5 as a cut‐off we obtained a sensitivity of 50% and a specificity of 96% for the diagnosis of FGR, while for IFC these values were respectively 27% and 73%. Expression of miR‐132 was associated with BW centile but not with CPR MoM. Finally, the best detection of IFC was achieved combining miR‐132 expression and CPR MoM (AUC = 0.69, p < 0.05). CONCLUSION: Fetuses with late‐onset FGR show upregulation of miR‐132. Further studies are needed to investigate the role of miR‐132 in the management of late‐onset FGR. John Wiley and Sons Inc. 2022-03-15 /pmc/articles/PMC8922531/ /pubmed/35317418 http://dx.doi.org/10.1002/hsr2.558 Text en © 2022 The Authors. Health Science Reports published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Morales‐Roselló, José
Loscalzo, Gabriela
García‐Lopez, Eva María
García‐Gimenez, José Luis
Perales‐Marín, Alfredo
MicroRNA‐132 is overexpressed in fetuses with late‐onset fetal growth restriction
title MicroRNA‐132 is overexpressed in fetuses with late‐onset fetal growth restriction
title_full MicroRNA‐132 is overexpressed in fetuses with late‐onset fetal growth restriction
title_fullStr MicroRNA‐132 is overexpressed in fetuses with late‐onset fetal growth restriction
title_full_unstemmed MicroRNA‐132 is overexpressed in fetuses with late‐onset fetal growth restriction
title_short MicroRNA‐132 is overexpressed in fetuses with late‐onset fetal growth restriction
title_sort microrna‐132 is overexpressed in fetuses with late‐onset fetal growth restriction
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8922531/
https://www.ncbi.nlm.nih.gov/pubmed/35317418
http://dx.doi.org/10.1002/hsr2.558
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