Literature DB >> 32099997

Interest in expanded carrier screening among individuals and couples in the general population: systematic review of the literature.

Eva Van Steijvoort1, Davit Chokoshvili1, Jeffrey W Cannon2, Hilde Peeters3, Karen Peeraer4, Gert Matthijs5, Pascal Borry1.   

Abstract

BACKGROUND: Through carrier screening, prospective parents can acquire information about whether they have an increased risk of conceiving a child affected with an autosomal recessive or X-linked condition. Within the last decade, advances in genomic technologies have facilitated a shift from condition-directed carrier screening to expanded carrier screening (ECS). Following the introduction of ECS, several studies have been performed to gauge the interest in this new technology among individuals and couples in the general population. OBJECTIVE AND RATIONALE: The aim of this systematic review was to synthesize evidence from empirical studies that assess the interest in ECS among individuals and couples in the general population. As the availability and accessibility of ECS grow, more couples who are a priori not at risk based on their personal or family history will be presented with the choice to accept or decline such an offer. Their attitudes and beliefs, as well as the perceived usefulness of this screening modality, will likely determine whether ECS is to become a widespread reproductive genetic test. SEARCH
METHODS: Four databases (Pubmed, Web of Science, CINAHL, Cochrane Library) were systematically searched to identify English language studies performed between January 2009 and January 2019 using the following search terms: carrier screening, carrier testing, attitudes, intention, interest, views, opinions, perspectives and uptake. Studies were eligible for inclusion if they reported on intentions to undergo a (hypothetical) ECS test, uptake of an actual ECS offer or both. Two researchers performed a multistep selection process independently for validation purposes. OUTCOMES: Twelve empirical studies performed between 2015 and 2019 were included for analysis. The studies originated from the USA (n = 6), the Netherlands (n = 3), Belgium (n = 1), Sweden (n = 1) and Australia (n = 1). The sample size of the studies varied from 80 to 1669. In the included studies, 32%-76% of respondents were interested in a (hypothetical) ECS test, while uptake rates for actual ECS offers ranged from 8% to 50%. The highest overall uptake was observed when ECS was offered to pregnant women (50%). By contrast, studies focusing on the preconception population reported lower overall uptake rates (8-34%) with the exception of one study where women were counseled preconception in preparation for IVF (68.7%). WIDER IMPLICATIONS: Our findings suggest that there may be discrepancies between prospective parents' reported intentions to undergo ECS and their actual uptake, particularly during the preconception period. As ECS is a new and relatively unknown test for most future parents, the awareness and comprehension within the general population could be rather limited. Adequate pre- and post-test counseling services should be made available to couples offered ECS to ensure informed reproductive decision-making, together with guidelines for primary health care professionals. Due to restricted nature of the samples and methods of the underlying primary studies, some of the reported results might not be transferable to a broader population. More research is needed to see if the observed trends also apply to a broader and more diverse population.
© The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please e-mail: journals.permission@oup.com.

Entities:  

Keywords:  attitudes; expanded carrier screening; intention; interest; reproductive genetics; uptake

Year:  2020        PMID: 32099997     DOI: 10.1093/humupd/dmaa001

Source DB:  PubMed          Journal:  Hum Reprod Update        ISSN: 1355-4786            Impact factor:   15.610


  8 in total

Review 1.  Societal implications of expanded universal carrier screening: a scoping review.

Authors:  Lieke M van den Heuvel; Nina van den Berg; A Cecile J W Janssens; Erwin Birnie; Lidewij Henneman; Wybo J Dondorp; Mirjam Plantinga; Irene M van Langen
Journal:  Eur J Hum Genet       Date:  2022-09-12       Impact factor: 5.351

2.  Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders.

Authors:  Ivy van Dijke; Carla G van El; Phillis Lakeman; Mariëtte Goddijn; Tessel Rigter; Martina C Cornel; Lidewij Henneman
Journal:  PLoS One       Date:  2022-06-21       Impact factor: 3.752

3.  Preconception expanded carrier screening: a focus group study with relatives of mucopolysaccharidosis type III patients and the general population.

Authors:  Thirsa Conijn; Ivy van Dijke; Lotte Haverman; Phillis Lakeman; Frits A Wijburg; Lidewij Henneman
Journal:  J Community Genet       Date:  2021-03-22

4.  Direct to consumer genetic testing in Denmark-public knowledge, use, and attitudes.

Authors:  Anne-Marie Gerdes; Line Nicolaisen; Egil Husum; Janne Bayer Andersen; Martin Dræbye Gantzhorn; Laura Roos; Birgitte Rode Diness
Journal:  Eur J Hum Genet       Date:  2021-03-01       Impact factor: 5.351

5.  Interest in Cancer Predisposition Testing and Carrier Screening Offered as Part of Routine Healthcare Among an Ethnically Diverse Sample of Young Women.

Authors:  Kimberly A Kaphingst; Jemar R Bather; Brianne M Daly; Daniel Chavez-Yenter; Alexis Vega; Wendy K Kohlmann
Journal:  Front Genet       Date:  2022-04-14       Impact factor: 4.772

6.  Views of patients and parents of children with genetic disorders on population-based expanded carrier screening.

Authors:  Anke J Woudstra; Lieke M van den Heuvel; Elsbeth H van Vliet-Lachotzki; Wybo Dondorp; Phillis Lakeman; Lotte Haverman; Irene M van Langen; Lidewij Henneman
Journal:  Prenat Diagn       Date:  2022-07-09       Impact factor: 3.242

Review 7.  Molecular Diagnosis and Genetic Counseling of Cystic Fibrosis and Related Disorders: New Challenges.

Authors:  Thierry Bienvenu; Maureen Lopez; Emmanuelle Girodon
Journal:  Genes (Basel)       Date:  2020-06-04       Impact factor: 4.096

8.  Specialist physicians' referral behavior regarding preimplantation genetic testing for single-gene disorders: Is there room to grow?

Authors:  Sarah Capelouto; Melanie Evans; Jennifer Shannon; Katelyn Jetelina; Orhan Bukulmez; Bruce Carr
Journal:  F S Rep       Date:  2021-03-11
  8 in total

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