Evidence map›Paper›PMID 39669632›Full record

ArticleGenetics in medicine open2024

Shortcomings of ethnicity-based carrier screening for conditions associated with Ashkenazi Jewish ancestry.

Hannah Llorin, Ruth Tennen, Sarah Laskey, Jianan Zhan, Stacey Detweiler, Noura S Abul-Husn

Abstract read
In one paragraph

Article in Genetics in medicine open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hannah Llorin23andMe, Inc, Sunnyvale, CA.
Ruth Tennen23andMe, Inc, Sunnyvale, CA.
Sarah Laskey23andMe, Inc, Sunnyvale, CA.
Jianan Zhan23andMe, Inc, Sunnyvale, CA.
Stacey Detweiler23andMe, Inc, Sunnyvale, CA.
Noura S Abul-Husn23andMe, Inc, Sunnyvale, CA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Carrier screening identifies reproductive risk for autosomal recessive and X-linked genetic conditions. Currently, some medical society guidelines continue to recommend ethnicity-based carrier screening for conditions associated with Ashkenazi Jewish (AJ) ancestry. We assessed the utility and limitations of these guidelines in a large, ethnically and genetically diverse cohort of genotyped individuals. Methods: We characterized the self-reported ethnicity and genetic ancestry of over 110,000 consenting research participants identified as heterozygous for pathogenic variants associated with 15 autosomal recessive conditions recommended by the American College of Obstetricians and Gynecologists for screening in individuals of AJ descent. Results: Out of 7.2 million research participants, 116,517 research participants were identified as heterozygous for pathogenic variants associated with 15 conditions evaluated. The majority (54.9%) of heterozygotes did not report qualifying ethnicity under American College of Obstetricians and Gynecologists ethnicity-based screening guidelines. Approximately half (51.3%) of all individuals heterozygous for pathogenic variants in genes associated with 1 or more conditions recommended to be screened exclusively in individuals of AJ descent had <20% computed AJ ancestry. Conclusion: Ethnicity-based carrier screening leads to the under detection of heterozygotes and associated reproductive risk for conditions historically associated with AJ ancestry.

Indexed as

Carrier screeningEthnicityGenetic ancestryPan-ethnic screeningRecessive disease

Identifiers

PMID39669632
PMCPMC11613755

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