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Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples
Expanded carrier screening (ECS) analyzes dozens or hundreds of recessive genes to determine reproductive risk. Data on the clinical utility of screening conditions beyond professional guidelines are scarce. Individuals underwent ECS for up to 110 genes. Five-hundred thirty-seven at-risk couples (AR...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943379/ https://www.ncbi.nlm.nih.gov/pubmed/28956228 http://dx.doi.org/10.1007/s10897-017-0160-1 |
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author | Ghiossi, Caroline E. Goldberg, James D. Haque, Imran S. Lazarin, Gabriel A. Wong, Kenny K. |
author_facet | Ghiossi, Caroline E. Goldberg, James D. Haque, Imran S. Lazarin, Gabriel A. Wong, Kenny K. |
author_sort | Ghiossi, Caroline E. |
collection | PubMed |
description | Expanded carrier screening (ECS) analyzes dozens or hundreds of recessive genes to determine reproductive risk. Data on the clinical utility of screening conditions beyond professional guidelines are scarce. Individuals underwent ECS for up to 110 genes. Five-hundred thirty-seven at-risk couples (ARC), those in which both partners carry the same recessive disease, were invited to participate in a retrospective IRB-approved survey of their reproductive decision making after receiving ECS results. Sixty-four eligible ARC completed the survey. Of 45 respondents screened preconceptionally, 62% (n = 28) planned IVF with PGD or prenatal diagnosis (PNDx) in future pregnancies. Twenty-nine percent (n = 13) were not planning to alter reproductive decisions. The remaining 9% (n = 4) of responses were unclear. Of 19 pregnant respondents, 42% (n = 8) elected PNDx, 11% (n = 2) planned amniocentesis but miscarried, and 47% (n = 9) considered the condition insufficiently severe to warrant invasive testing. Of the 8 pregnancies that underwent PNDx, 5 were unaffected and 3 were affected. Two of 3 affected pregnancies were terminated. Disease severity was found to have significant association (p = 0.000145) with changes in decision making, whereas guideline status of diseases, controlled for severity, was not (p = 0.284). Most ARC altered reproductive planning, demonstrating the clinical utility of ECS. Severity of conditions factored into decision making. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10897-017-0160-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5943379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-59433792018-05-14 Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples Ghiossi, Caroline E. Goldberg, James D. Haque, Imran S. Lazarin, Gabriel A. Wong, Kenny K. J Genet Couns Original Research Expanded carrier screening (ECS) analyzes dozens or hundreds of recessive genes to determine reproductive risk. Data on the clinical utility of screening conditions beyond professional guidelines are scarce. Individuals underwent ECS for up to 110 genes. Five-hundred thirty-seven at-risk couples (ARC), those in which both partners carry the same recessive disease, were invited to participate in a retrospective IRB-approved survey of their reproductive decision making after receiving ECS results. Sixty-four eligible ARC completed the survey. Of 45 respondents screened preconceptionally, 62% (n = 28) planned IVF with PGD or prenatal diagnosis (PNDx) in future pregnancies. Twenty-nine percent (n = 13) were not planning to alter reproductive decisions. The remaining 9% (n = 4) of responses were unclear. Of 19 pregnant respondents, 42% (n = 8) elected PNDx, 11% (n = 2) planned amniocentesis but miscarried, and 47% (n = 9) considered the condition insufficiently severe to warrant invasive testing. Of the 8 pregnancies that underwent PNDx, 5 were unaffected and 3 were affected. Two of 3 affected pregnancies were terminated. Disease severity was found to have significant association (p = 0.000145) with changes in decision making, whereas guideline status of diseases, controlled for severity, was not (p = 0.284). Most ARC altered reproductive planning, demonstrating the clinical utility of ECS. Severity of conditions factored into decision making. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10897-017-0160-1) contains supplementary material, which is available to authorized users. Springer US 2017-09-27 2018 /pmc/articles/PMC5943379/ /pubmed/28956228 http://dx.doi.org/10.1007/s10897-017-0160-1 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Ghiossi, Caroline E. Goldberg, James D. Haque, Imran S. Lazarin, Gabriel A. Wong, Kenny K. Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples |
title | Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples |
title_full | Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples |
title_fullStr | Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples |
title_full_unstemmed | Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples |
title_short | Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples |
title_sort | clinical utility of expanded carrier screening: reproductive behaviors of at-risk couples |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943379/ https://www.ncbi.nlm.nih.gov/pubmed/28956228 http://dx.doi.org/10.1007/s10897-017-0160-1 |
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