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Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population
Background and Objectives: Non-invasive prenatal testing (NIPT) has been confirmed as the most accurate screening test for trisomies 21, 18, 13, sex chromosomes aneuploidies and several microdeletions. This study aimed to assess the accuracy of cell free DNA testing based on low-level whole-genome s...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777823/ https://www.ncbi.nlm.nih.gov/pubmed/35056387 http://dx.doi.org/10.3390/medicina58010079 |
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author | Gug, Cristina Mozos, Ioana Ratiu, Adrian Tudor, Anca Gorduza, Eusebiu Vlad Caba, Lavinia Gug, Miruna Cojocariu, Catalina Furau, Cristian Furau, Gheorghe Vaida, Monica Adriana Stoicanescu, Dorina |
author_facet | Gug, Cristina Mozos, Ioana Ratiu, Adrian Tudor, Anca Gorduza, Eusebiu Vlad Caba, Lavinia Gug, Miruna Cojocariu, Catalina Furau, Cristian Furau, Gheorghe Vaida, Monica Adriana Stoicanescu, Dorina |
author_sort | Gug, Cristina |
collection | PubMed |
description | Background and Objectives: Non-invasive prenatal testing (NIPT) has been confirmed as the most accurate screening test for trisomies 21, 18, 13, sex chromosomes aneuploidies and several microdeletions. This study aimed to assess the accuracy of cell free DNA testing based on low-level whole-genome sequencing to screen for these chromosomal abnormalities and to evaluate the clinical performance of NIPT. Materials and Methods: 380 consecutive cases from a single genetic center, from Western Romania were included in this retrospective study. Cell-free nucleic acid extraction from maternal blood, DNA sequencing and analysis of sequenced regions were performed by BGI Hong Kong and Invitae USA to determine the risk of specific fetal chromosomal abnormalities. In high-risk cases the results were checked by direct analysis of fetal cells obtained by invasive methods: 6 chorionic villus sampling and 10 amniocenteses followed by combinations of QF-PCR, karyotyping and aCGH. Results: NIPT results indicated low risk in 95.76% of cases and high risk in 4.23%. Seven aneuploidies and one microdeletion were confirmed, the other results were found to be a false-positive. A gestational age of up to 22 weeks had no influence on fetal fraction. There were no significant differences in fetal fraction across the high and low risk groups. Conclusions: This is the first study in Romania to report the NIPT results. The confirmation rate was higher for autosomal aneuploidies compared to sex chromosome aneuploidies and microdeletions. All cases at risk for trisomy 21 were confirmed. Only one large fetal microdeletion detected by NIPT has been confirmed. False positive NIPT results, not confirmed by invasive methods, led to the decision to continue the pregnancy. The main limitation of the study is the small number of patients included. NIPT can be used as a screening method for all pregnancies, but in high-risk cases, an invasive confirmation test was performed. |
format | Online Article Text |
id | pubmed-8777823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87778232022-01-22 Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population Gug, Cristina Mozos, Ioana Ratiu, Adrian Tudor, Anca Gorduza, Eusebiu Vlad Caba, Lavinia Gug, Miruna Cojocariu, Catalina Furau, Cristian Furau, Gheorghe Vaida, Monica Adriana Stoicanescu, Dorina Medicina (Kaunas) Article Background and Objectives: Non-invasive prenatal testing (NIPT) has been confirmed as the most accurate screening test for trisomies 21, 18, 13, sex chromosomes aneuploidies and several microdeletions. This study aimed to assess the accuracy of cell free DNA testing based on low-level whole-genome sequencing to screen for these chromosomal abnormalities and to evaluate the clinical performance of NIPT. Materials and Methods: 380 consecutive cases from a single genetic center, from Western Romania were included in this retrospective study. Cell-free nucleic acid extraction from maternal blood, DNA sequencing and analysis of sequenced regions were performed by BGI Hong Kong and Invitae USA to determine the risk of specific fetal chromosomal abnormalities. In high-risk cases the results were checked by direct analysis of fetal cells obtained by invasive methods: 6 chorionic villus sampling and 10 amniocenteses followed by combinations of QF-PCR, karyotyping and aCGH. Results: NIPT results indicated low risk in 95.76% of cases and high risk in 4.23%. Seven aneuploidies and one microdeletion were confirmed, the other results were found to be a false-positive. A gestational age of up to 22 weeks had no influence on fetal fraction. There were no significant differences in fetal fraction across the high and low risk groups. Conclusions: This is the first study in Romania to report the NIPT results. The confirmation rate was higher for autosomal aneuploidies compared to sex chromosome aneuploidies and microdeletions. All cases at risk for trisomy 21 were confirmed. Only one large fetal microdeletion detected by NIPT has been confirmed. False positive NIPT results, not confirmed by invasive methods, led to the decision to continue the pregnancy. The main limitation of the study is the small number of patients included. NIPT can be used as a screening method for all pregnancies, but in high-risk cases, an invasive confirmation test was performed. MDPI 2022-01-05 /pmc/articles/PMC8777823/ /pubmed/35056387 http://dx.doi.org/10.3390/medicina58010079 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gug, Cristina Mozos, Ioana Ratiu, Adrian Tudor, Anca Gorduza, Eusebiu Vlad Caba, Lavinia Gug, Miruna Cojocariu, Catalina Furau, Cristian Furau, Gheorghe Vaida, Monica Adriana Stoicanescu, Dorina Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population |
title | Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population |
title_full | Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population |
title_fullStr | Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population |
title_full_unstemmed | Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population |
title_short | Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population |
title_sort | genetic counseling and management: the first study to report nipt findings in a romanian population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777823/ https://www.ncbi.nlm.nih.gov/pubmed/35056387 http://dx.doi.org/10.3390/medicina58010079 |
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