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MicroRNA changes in maternal serum from pregnancies complicated by twin‐twin transfusion syndrome: A discovery study
OBJECTIVE: MicroRNAs (miRNAs) are used as biomarkers in cardiovascular disease and cancer. miRNAs are involved in placental development but have not previously been investigated in twin‐twin transfusion syndrome (TTTS). Our aim is to explore the miRNA profile of TTTS pregnancies. METHOD: Initial miR...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771789/ https://www.ncbi.nlm.nih.gov/pubmed/31077410 http://dx.doi.org/10.1002/pd.5475 |
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author | Mackie, Fiona L. Baker, Bernadette C. Beggs, Andrew D. Stodolna, Agata Morris, Rachel Katie Kilby, Mark D. |
author_facet | Mackie, Fiona L. Baker, Bernadette C. Beggs, Andrew D. Stodolna, Agata Morris, Rachel Katie Kilby, Mark D. |
author_sort | Mackie, Fiona L. |
collection | PubMed |
description | OBJECTIVE: MicroRNAs (miRNAs) are used as biomarkers in cardiovascular disease and cancer. miRNAs are involved in placental development but have not previously been investigated in twin‐twin transfusion syndrome (TTTS). Our aim is to explore the miRNA profile of TTTS pregnancies. METHOD: Initial miRNA profiling was performed using a reverse transcription polymerase chain reaction (RT‐PCR) panel on maternal serum samples taken from five women prior to fetoscopic laser ablation for TTTS and compared with serum samples from five women with uncomplicated monochorionic diamniotic twin pregnancies. Validation RT‐PCR was performed in an additional cohort of eight TTTS pregnancies and eight uncomplicated pregnancies. RESULTS: Median gestational age at sampling in the TTTS and control groups was 20(+0) weeks (interquartile range [IQR], 19(+4)‐20(+0)) and 20(+2) weeks (IQR, 20(+0)‐20(+2)), respectively. All samples passed quality control. One control sample was excluded as a biological outlier. Thirty‐one of 752 miRNAs were significantly different: 17 were upregulated and 14 downregulated in the TTTS group, although they did not remain significant following Benjamini‐Hochberg correction for multiple testing. The six miRNAs chosen for validation demonstrated no significant difference. CONCLUSION: This is the first study to investigate miRNA changes in TTTS pregnancies. We did not demonstrate a statistically significant difference in miRNAs in TTTS pregnancies, but further investigation is required. |
format | Online Article Text |
id | pubmed-6771789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67717892019-10-07 MicroRNA changes in maternal serum from pregnancies complicated by twin‐twin transfusion syndrome: A discovery study Mackie, Fiona L. Baker, Bernadette C. Beggs, Andrew D. Stodolna, Agata Morris, Rachel Katie Kilby, Mark D. Prenat Diagn Original Articles OBJECTIVE: MicroRNAs (miRNAs) are used as biomarkers in cardiovascular disease and cancer. miRNAs are involved in placental development but have not previously been investigated in twin‐twin transfusion syndrome (TTTS). Our aim is to explore the miRNA profile of TTTS pregnancies. METHOD: Initial miRNA profiling was performed using a reverse transcription polymerase chain reaction (RT‐PCR) panel on maternal serum samples taken from five women prior to fetoscopic laser ablation for TTTS and compared with serum samples from five women with uncomplicated monochorionic diamniotic twin pregnancies. Validation RT‐PCR was performed in an additional cohort of eight TTTS pregnancies and eight uncomplicated pregnancies. RESULTS: Median gestational age at sampling in the TTTS and control groups was 20(+0) weeks (interquartile range [IQR], 19(+4)‐20(+0)) and 20(+2) weeks (IQR, 20(+0)‐20(+2)), respectively. All samples passed quality control. One control sample was excluded as a biological outlier. Thirty‐one of 752 miRNAs were significantly different: 17 were upregulated and 14 downregulated in the TTTS group, although they did not remain significant following Benjamini‐Hochberg correction for multiple testing. The six miRNAs chosen for validation demonstrated no significant difference. CONCLUSION: This is the first study to investigate miRNA changes in TTTS pregnancies. We did not demonstrate a statistically significant difference in miRNAs in TTTS pregnancies, but further investigation is required. John Wiley and Sons Inc. 2019-06-18 2019-07 /pmc/articles/PMC6771789/ /pubmed/31077410 http://dx.doi.org/10.1002/pd.5475 Text en © 2019 The Authors. Prenatal Diagnosis Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://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 Articles Mackie, Fiona L. Baker, Bernadette C. Beggs, Andrew D. Stodolna, Agata Morris, Rachel Katie Kilby, Mark D. MicroRNA changes in maternal serum from pregnancies complicated by twin‐twin transfusion syndrome: A discovery study |
title | MicroRNA changes in maternal serum from pregnancies complicated by twin‐twin transfusion syndrome: A discovery study |
title_full | MicroRNA changes in maternal serum from pregnancies complicated by twin‐twin transfusion syndrome: A discovery study |
title_fullStr | MicroRNA changes in maternal serum from pregnancies complicated by twin‐twin transfusion syndrome: A discovery study |
title_full_unstemmed | MicroRNA changes in maternal serum from pregnancies complicated by twin‐twin transfusion syndrome: A discovery study |
title_short | MicroRNA changes in maternal serum from pregnancies complicated by twin‐twin transfusion syndrome: A discovery study |
title_sort | microrna changes in maternal serum from pregnancies complicated by twin‐twin transfusion syndrome: a discovery study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771789/ https://www.ncbi.nlm.nih.gov/pubmed/31077410 http://dx.doi.org/10.1002/pd.5475 |
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