Document Type
Article
Publication Date
7-10-2024
Abstract
Sex chromosome aneuploidies (SCAs) collectively occur in 1 in 500 livebirths, and diagnoses in the neonatal period are increasing with advancements in prenatal and early genetic testing. Inevitably, SCA will be identified on either routine prenatal or newborn screening in the near future. Tetrasomy SCAs are rare, manifesting more significant phenotypes compared to trisomies. Prenatal cell-free DNA (cfDNA) screening has been demonstrated to have relatively poor positive predictive values (PPV) in SCAs, directing genetic counseling discussions towards false-positive likelihood rather than thoroughly addressing all possible outcomes and phenotypes, respectively. The eXtraordinarY Babies study is a natural history study of children prenatally identified with SCAs, and it developed a longitudinal data resource and common data elements with the Newborn Screening Translational Research Network (NBSTRN). A review of cfDNA and diagnostic reports from participants identified a higher than anticipated rate of discordance. The aims of this project are to (1) compare our findings to outcomes from a regional clinical cytogenetic laboratory and (2) describe discordant outcomes from both samples. Twenty-one (10%), and seven (8.3%) cases were found to be discordant between cfDNA (result or indication reported to lab) and diagnosis for the Babies Study and regional laboratory, respectively. Discordant results represented six distinct discordance categories when comparing cfDNA to diagnostic results, with the largest groups being Trisomy cfDNA vs. Tetrasomy diagnosis (66.7% of discordance in eXtraordinarY Babies study) and Mosaicism (57.1% in regional laboratory). Traditional genetic counseling for SCA-related cfDNA results is inadequate given a high degree of discordance that jeopardizes the accuracy of the information discussed and informed decision making following prenatal genetic counseling.
Recommended Citation
Howell, Susan; Davis, Shanlee M.; Carstens, Billie; Haag, Mary; Ross, Judith L.; and Tartaglia, Nicole R., "Discordant Prenatal Cell-Free DNA Screening vs. Diagnostic Results of Sex Chromosome Aneuploidies: Implications for Newborn Screening and Genetic Counseling" (2024). Department of Pediatrics Faculty Papers. Paper 162.
https://jdc.jefferson.edu/pedsfp/162
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
PubMed ID
39051404
Language
English
Included in
Diagnosis Commons, Genetic Phenomena Commons, Health Services Research Commons, Pediatrics Commons
Comments
This article is the author's final published version in International Journal of Neonatal Screening, Volume 10, Issue 3, September 2024, Article number 48.
The published version is available at https://doi.org/10.3390/ijns10030048.
Copyright © 2024 by the authors