Customizing carrier screening in the Chinese population: Insights from a 334-gene panel.

IF 2.7 2区 医学 Q2 GENETICS & HEREDITY Prenatal Diagnosis Pub Date : 2024-10-01 Epub Date: 2024-07-18 DOI:10.1002/pd.6635
Sha Liu, Shuang Huang, Victor Wei Zhang, Liyuan Cao, Haipeng Liu, Xiang Wei, Yuan Luo, Yue Li, Lin Zhou, Fuping Li, Qian Zhu, Hongqian Liu
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Abstract

Objective: This study aimed to evaluate the yield and applicability of expanded carrier screening and propose carrier rate screening thresholds suitable for the Chinese population by comparing the current screening panel with the American College of Medical Genetics and Genomics recommended panel of 113 genes.

Methods: Using targeted next-generation sequencing, a customized panel with 334 genes was performed on 2168 individuals without clinical phenotypes for expanded carrier screening purpose. Variant interpretation followed the American College of Medical Genetics and Genomics guidelines. Carrier rates were calculated for each identified variant and each gene. At-risk couple rates were also assessed. The yield of expanded carrier screening was evaluated through calculating cumulative carrier rate.

Results: Overall, 65.87% of the individuals were found to be carriers of at least 1 disease causing variants. The overall at-risk couple rate was 11.76%, of which the GJB2:c.109G > A related at-risk couple rate was 5.78%. The cumulative carrier rate of 334-panel was 65.53%. When screened genes with gene carrier rate ≥1/1000, the expanded carrier screening can cover over 90% of the cumulative carrier rate and at-risk couples. A total of 86 genes overlapped with American College of Medical Genetics and Genomics Tier-3 genes and were attributed to the cumulative carrier rate of 47.33%.

Conclusion: Expanded carrier screening using the 334-gene panel showed high screening efficiency. A threshold of gene carrier rate ≥1/1000 is recommended for selecting carrier screening genes in the Chinese Han population. This study highlights the importance of customizing screening panels based on the ACMG Tier-3 genes in conjunction with population-specific carrier frequencies to improve the accuracy and effectiveness of expanded carrier screening.

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在中国人群中定制携带者筛查:来自 334 个基因面板的启示。
目的:本研究旨在评估扩大携带者筛查的收益和适用性,并通过比较目前的筛查面板和美国医学遗传学和基因组学学院推荐的113个基因面板,提出适合中国人群的携带率筛查阈值:方法:利用有针对性的新一代测序技术,对2168名无临床表型的个体进行了包含334个基因的定制面板,以达到扩大携带者筛查的目的。变异解释遵循美国医学遗传学和基因组学学院指南。计算了每个已确定变异和每个基因的携带率。同时还评估了高危夫妇率。通过计算累计携带者率来评估扩大携带者筛查的收益:结果:总体而言,65.87% 的个体被发现是至少一种致病变异的携带者。总体高危夫妇率为 11.76%,其中 GJB2:c.109G > A 相关高危夫妇率为 5.78%。334 个面板的累计携带率为 65.53%。当筛查基因携带率≥1/1000时,扩大携带者筛查可覆盖90%以上的累计携带率和高危夫妇。共有 86 个基因与美国医学遗传学和基因组学学会三级基因重叠,累计携带率为 47.33%:结论:使用334个基因面板进行扩大的携带者筛查显示出很高的筛查效率。建议在中国汉族人群中选择基因携带者筛查基因时,阈值为基因携带率≥1/1000。本研究强调了根据 ACMG Tier-3 基因并结合特定人群的携带者频率定制筛查面板对提高扩大携带者筛查的准确性和有效性的重要性。
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来源期刊
Prenatal Diagnosis
Prenatal Diagnosis 医学-妇产科学
CiteScore
5.80
自引率
13.30%
发文量
204
审稿时长
2 months
期刊介绍: Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling
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