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First French study relative to preconception genetic testing: 1500 general population participants’ opinion
BACKGROUND: Until very recently, preconception genetic testing was only conducted in particular communities, ethnic groups or families for which an increased risk of genetic disease was identified. To detect in general population a risk for a couple to have a child affected by a rare, recessive or X...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955630/ https://www.ncbi.nlm.nih.gov/pubmed/33712027 http://dx.doi.org/10.1186/s13023-021-01754-z |
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author | Bonneau, Valérie Nizon, Mathilde Latypova, Xenia Gaultier, Aurélie Hoarau, Eugénie Bézieau, Stéphane Minguet, Guy Turrini, Mauro Jourdain, Maud Isidor, Bertrand |
author_facet | Bonneau, Valérie Nizon, Mathilde Latypova, Xenia Gaultier, Aurélie Hoarau, Eugénie Bézieau, Stéphane Minguet, Guy Turrini, Mauro Jourdain, Maud Isidor, Bertrand |
author_sort | Bonneau, Valérie |
collection | PubMed |
description | BACKGROUND: Until very recently, preconception genetic testing was only conducted in particular communities, ethnic groups or families for which an increased risk of genetic disease was identified. To detect in general population a risk for a couple to have a child affected by a rare, recessive or X-linked, genetic disease, carrier screening is proposed in several countries. We aimed to determine the current public opinion relative to this approach in France, using either a printed or web-based questionnaire. RESULTS: Among the 1568 participants, 91% are favorable to preconception genetic tests and 57% declare to be willing to have the screening if the latter is available. A medical prescription by a family doctor or a gynecologist would be the best way to propose the test for 73%, with a reimbursement from the social security insurance. However, 19% declare not to be willing to use the test because of their ethic or moral convictions, and the fear that the outcome would question the pregnancy. Otherwise, most participants consider that the test is a medical progress despite the risk of an increased medicalization of the pregnancy. CONCLUSION: This first study in France highlights a global favorable opinion for the preconception genetic carrier testing under a medical prescription and a reimbursement by social security insurance. Our results emphasize as well the complex concerns underpinned by the use of this screening strategy. Therefore, the ethical issues related to these tests include the risk of eugenic drift mentioned by more than half of the participants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-01754-z. |
format | Online Article Text |
id | pubmed-7955630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79556302021-03-15 First French study relative to preconception genetic testing: 1500 general population participants’ opinion Bonneau, Valérie Nizon, Mathilde Latypova, Xenia Gaultier, Aurélie Hoarau, Eugénie Bézieau, Stéphane Minguet, Guy Turrini, Mauro Jourdain, Maud Isidor, Bertrand Orphanet J Rare Dis Research BACKGROUND: Until very recently, preconception genetic testing was only conducted in particular communities, ethnic groups or families for which an increased risk of genetic disease was identified. To detect in general population a risk for a couple to have a child affected by a rare, recessive or X-linked, genetic disease, carrier screening is proposed in several countries. We aimed to determine the current public opinion relative to this approach in France, using either a printed or web-based questionnaire. RESULTS: Among the 1568 participants, 91% are favorable to preconception genetic tests and 57% declare to be willing to have the screening if the latter is available. A medical prescription by a family doctor or a gynecologist would be the best way to propose the test for 73%, with a reimbursement from the social security insurance. However, 19% declare not to be willing to use the test because of their ethic or moral convictions, and the fear that the outcome would question the pregnancy. Otherwise, most participants consider that the test is a medical progress despite the risk of an increased medicalization of the pregnancy. CONCLUSION: This first study in France highlights a global favorable opinion for the preconception genetic carrier testing under a medical prescription and a reimbursement by social security insurance. Our results emphasize as well the complex concerns underpinned by the use of this screening strategy. Therefore, the ethical issues related to these tests include the risk of eugenic drift mentioned by more than half of the participants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-01754-z. BioMed Central 2021-03-12 /pmc/articles/PMC7955630/ /pubmed/33712027 http://dx.doi.org/10.1186/s13023-021-01754-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Bonneau, Valérie Nizon, Mathilde Latypova, Xenia Gaultier, Aurélie Hoarau, Eugénie Bézieau, Stéphane Minguet, Guy Turrini, Mauro Jourdain, Maud Isidor, Bertrand First French study relative to preconception genetic testing: 1500 general population participants’ opinion |
title | First French study relative to preconception genetic testing: 1500 general population participants’ opinion |
title_full | First French study relative to preconception genetic testing: 1500 general population participants’ opinion |
title_fullStr | First French study relative to preconception genetic testing: 1500 general population participants’ opinion |
title_full_unstemmed | First French study relative to preconception genetic testing: 1500 general population participants’ opinion |
title_short | First French study relative to preconception genetic testing: 1500 general population participants’ opinion |
title_sort | first french study relative to preconception genetic testing: 1500 general population participants’ opinion |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955630/ https://www.ncbi.nlm.nih.gov/pubmed/33712027 http://dx.doi.org/10.1186/s13023-021-01754-z |
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