Considering severity in the design of reproductive genetic carrier screening programs: screening for severe conditions

Reproductive genetic carrier screening (RGCS) provides information about people's chance of having children with certain genetic conditions, to inform reproductive decision making. RGCS at population scale requires a robust and streamlined program that is purposively designed and formally implemented to ensure equity and consistency. There are many considerations in selecting conditions, genes and variants for inclusion in RGCS, with severity of the genetic condition a key criterion. However, the concept of severity is complex and often underspecified in available guidelines. Severity is often determined in relation to other contextual features and can be experienced differently by individuals who all have the same condition. While some genetic conditions are unambiguously considered severe, there are many factors that contribute to how severe a condition is perceived to be (and by whom), and perspectives will vary. In this paper, we analyse why severity is an important criterion when selecting conditions, genes or variants to be included in RGCS. We suggest that screening programs should be oriented more towards variants and genes associated with severe conditions. We discuss the importance of taking a practical approach to gene selection in a carrier screening program when presenting the offer at population scale.

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Publication Details

Journal
European Journal of Human Genetics
Published
2024-11-25
DOI
https://doi.org/10.1038/s41431-024-01738-0
Citations
4
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
1.68

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article

Considering severity in the design of reproductive genetic carrier screening programs: screening for severe conditions

Martin Bruce Delatycki, Nigel G. Laing, Edwin Philip Kirk, Lucinda Freeman et al.
4 citations
European Journal of Human Genetics
Cystic Fibrosis Research Advances
1.68
article

Considering severity in the design of reproductive genetic carrier screening programs: screening for severe conditions

Martin Bruce Delatycki, Nigel G. Laing, Edwin Philip Kirk, Lucinda Freeman, Alison D. Archibald, Lisa Dive, Ainsley J. Newson
article en
4 citations

Abstract

Reproductive genetic carrier screening (RGCS) provides information about people's chance of having children with certain genetic conditions, to inform reproductive decision making. RGCS at population scale requires a robust and streamlined program that is purposively designed and formally implemented to ensure equity and consistency. There are many considerations in selecting conditions, genes and variants for inclusion in RGCS, with severity of the genetic condition a key criterion. However, the concept of severity is complex and often underspecified in available guidelines. Severity is often determined in relation to other contextual features and can be experienced differently by individuals who all have the same condition. While some genetic conditions are unambiguously considered severe, there are many factors that contribute to how severe a condition is perceived to be (and by whom), and perspectives will vary. In this paper, we analyse why severity is an important criterion when selecting conditions, genes or variants to be included in RGCS. We suggest that screening programs should be oriented more towards variants and genes associated with severe conditions. We discuss the importance of taking a practical approach to gene selection in a carrier screening program when presenting the offer at population scale.

European Journal of Human GeneticsVol. 33(2)
University of Technology Sydney (AU), The University of Sydney (AU), New South Wales Department of Health (AU), The University of Western Australia (AU), Harry Perkins Institute of Medical Research (AU), Victorian Clinical Genetics Services (AU), Sydney Local Health District (AU), Sydney Children’s Hospitals Network (AU), Murdoch Children's Research Institute (AU)
Children’s Hospital of Wisconsin Research Institute, Murdoch Children's Research Institute, Australian Government, Department of Health and Aged Care, Australian Government
Reduced inequalities
Openalex Percentile: Top 14%
Cystic Fibrosis Research Advances
1.68
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