Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA: A survey study

Steffensen, Ellen Hollands, Skakkebæk, Anne, Gadsbøll, Kasper, Petersen, Olav Bjørn, Westover, Thomas, Strange, Heather ORCID: https://orcid.org/0000-0002-5758-8445, The NIPT‐SCA‐map Study Group and Vogel, Ida 2023. Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA: A survey study. Prenatal Diagnosis 43 (2) , pp. 144-155. 10.1002/pd.6322

[thumbnail of pd.6322.pdf] PDF - Published Version
Available under License Creative Commons Attribution Non-commercial.

Download (1MB)

Abstract

Objective: To examine the extent to which sex chromosomes are included in current noninvasive prenatal testing (NIPT) and the reporting practices with respect to fetal chromosomal sex and sex chromosome aberrations (SCAs), in addition to an update on the general implementation of NIPT. Method: A questionnaire addressing the research objectives was distributed by email to fetal medicine and clinical genetics experts in Asia, Australia, Europe and the USA. Results: Guidelines on NIPT are available in the majority of the included countries. Not all existing guidelines address reporting of fetal chromosomal sex and SCAs. In most settings, NIPT frequently includes sex chromosomes (five Australian states, China, Hong Kong, Israel, Singapore, Thailand, USA and 23 of 31 European countries). This occurs most often by default or when parents wish to know fetal sex. In most settings, a potential SCA is reported by stating the risk hereof as “low” or “high” and/or by naming the SCA. Less than 50% of all pregnant women receive NIPT according to respondents from three Australian states, China, Israel, Singapore, Thailand and 24 of 31 European countries. However, this percentage, the genomic coverage of NIPT and its application as primary or secondary screening vary by setting. Conclusion: In most of the studied countries/states, NIPT commonly includes sex chromosomes. The reporting practices concerning fetal chromosomal sex and SCAs are diverse and most commonly not addressed by guidelines. In general, NIPT is variably implemented across countries/states.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
Additional Information: License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by-nc/4.0/
Publisher: Wiley
ISSN: 0197-3851
Date of First Compliant Deposit: 9 February 2023
Date of Acceptance: 17 January 2023
Last Modified: 25 May 2023 12:14
URI: https://orca.cardiff.ac.uk/id/eprint/156600

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics