Challenges for the implementation of next generation sequencing-based expanded carrier screening: Lessons learned from the ciliopathies
Vintschger E, Kraemer D, Joset P, Horn A, Rauch A, Sticht H, Bachmann-Gagescu R (2022)
Publication Type: Journal article
Publication year: 2022
Journal
DOI: 10.1038/s41431-022-01267-8
Abstract
Next generation sequencing (NGS) can detect carrier status for rare recessive disorders, informing couples about their reproductive risk. The recent ACMG recommendations support offering NGS-based carrier screening (NGS-CS) in an ethnic and population-neutral manner for all genes that have a carrier frequency > 1/200 (based on GnomAD). To evaluate current challenges for NGS-CS, we focused on the ciliopathies, a well-studied group of rare recessive disorders. We analyzed 118 ciliopathy genes by whole exome sequencing in similar to 400 healthy local individuals and similar to 1000 individuals from the UK1958-birth cohort. We found 20% of healthy individuals (1% of couples) to be carriers of reportable variants in a ciliopathy gene, while 50% (4% of couples) carry variants of uncertain significance (VUS). This large proportion of VUS is partly explained by the limited utility of the ACMG/AMP variant-interpretation criteria in healthy individuals, where phenotypic match or segregation criteria cannot be used. Most missense variants are thus classified as VUS and not reported, which reduces the negative predictive value of the screening test. We show how gene-specific variation patterns and structural protein information can help prioritize variants most likely to be disease-causing, for (future) functional assays. Even when considering only strictly pathogenic variants, the observed carrier frequency is substantially higher than expected based on estimated disease prevalence, challenging the 1/200 carrier frequency cut-off proposed for choice of genes to screen. Given the challenges linked to variant interpretation in healthy individuals and the uncertainties about true carrier frequencies, genetic counseling must clearly disclose these limitations of NGS-CS.
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Switzerland (CH)How to cite
APA:
Vintschger, E., Kraemer, D., Joset, P., Horn, A., Rauch, A., Sticht, H., & Bachmann-Gagescu, R. (2022). Challenges for the implementation of next generation sequencing-based expanded carrier screening: Lessons learned from the ciliopathies. European Journal of Human Genetics. https://doi.org/10.1038/s41431-022-01267-8
MLA:
Vintschger, Ella, et al. "Challenges for the implementation of next generation sequencing-based expanded carrier screening: Lessons learned from the ciliopathies." European Journal of Human Genetics (2022).
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