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针对与阿什肯纳兹犹太血统相关疾病的基于种族的携带者筛查的缺点。

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

作者信息

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

机构信息

23andMe, Inc, Sunnyvale, CA.

出版信息

Genet Med Open. 2024 Jul 16;2:101869. doi: 10.1016/j.gimo.2024.101869. eCollection 2024.

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.

摘要

目的

携带者筛查可识别常染色体隐性和X连锁遗传病的生殖风险。目前,一些医学协会指南仍建议针对与阿什肯纳兹犹太(AJ)血统相关的疾病进行基于种族的携带者筛查。我们在一个种族和基因多样化的大型基因分型个体队列中评估了这些指南的实用性和局限性。

方法

我们对超过110,000名同意参与研究的参与者的自我报告种族和基因血统进行了特征分析,这些参与者被确定为与美国妇产科医师学会推荐的针对AJ血统个体进行筛查的15种常染色体隐性疾病相关的致病基因变异的杂合子。

结果

在720万研究参与者中,有116,517名研究参与者被确定为与所评估的15种疾病相关的致病基因变异的杂合子。根据美国妇产科医师学会基于种族的筛查指南,大多数(54.9%)杂合子未报告符合条件的种族。在与建议仅在AJ血统个体中筛查的1种或多种疾病相关基因的致病基因变异杂合子中,约一半(51.3%)的个体计算得出的AJ血统<20%。

结论

基于种族的携带者筛查导致杂合子漏检以及与历史上与AJ血统相关疾病的相关生殖风险漏检。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33bd/11613755/a01b9abea0fc/gr1.jpg

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