Suppr超能文献

[对3097名中国健康育龄个体进行216种疾病的扩展携带者筛查]

[Expanded carrier screening for 216 diseases in a cohort of 3 097 healthy Chinese individuals of childbearing age].

作者信息

Hao N, Yin K L, Zhang H Z, Qi Q W, Zhou X Y, Lyu Y, Jiang Y L

机构信息

Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, National Clinical Research Center for Obstetric and Gynecologic Diseases, Beijing 100730, China.

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2024 Oct 25;59(10):764-770. doi: 10.3760/cma.j.cn112141-20240617-00340.

Abstract

To determine the carrier frequency and hot-spot variants of a custom-designed expanded carrier screening (ECS) panel with 216 diseases (216-ECS panel) within a Chinese population of childbearing age. Whole-exome sequencing data from a cohort of 3 097 unrelated healthy individuals (including 1 424 couples) from Peking Union Medical College Hospital between January 2013 and December 2023 were analyzed. Totally 220 genes which inherited in a recessive manner of 216-ECS panel were included in the analysis. The analysis included variant carrier rate, gene carrier rate, cumulative carrier rate, at-risk couple rates, and variant spectrum. (1) Pathogenic variants were identified in 1 472 (47.53%, 1 472/3 097) individuals, with an average of 0.65 pathogenic variants per individual. The rate of at-risk couples was 3.93% (56/1 424). (2) A total of 180 genes were identified, with 16 genes exhibiting a gene carrier rate of ≥1% and 33 genes having a rate of ≥0.5%, most of which were associated with inherited metabolic diseases. Noteworthy genes with higher gene carrier rates and high-frequency variants included : c.235del, : c.728G>A, : c.2333G>T, : c.919-2A>G, : c.1901T>C, : c.2890C>T, : c.1472C>G, : c.2802T>G, : c.852_855del, : c.761C>T and c.752C>T. This study offers a focused analysis of carrier frequencies and hot-spot variants of 216 diseases of the ECS panel constructed by our laboratory among the Chinese population, laying a foundation for the development of ECS programs tailored to the Chinese population.

摘要

确定定制设计的包含216种疾病的扩展携带者筛查(ECS) panel(216-ECS panel)在中国育龄人群中的携带频率和热点变异。分析了2013年1月至2023年12月期间北京协和医院3097名无亲缘关系的健康个体(包括1424对夫妇)队列的全外显子测序数据。分析纳入了216-ECS panel中以隐性方式遗传的总共220个基因。分析包括变异携带者率、基因携带者率、累积携带者率、高危夫妇率和变异谱。(1)在1472名个体(47.53%,1472/3097)中鉴定出致病性变异,个体平均携带0.65个致病性变异。高危夫妇率为3.93%(56/1424)。(2)共鉴定出180个基因,其中16个基因的基因携带者率≥1%,33个基因的基因携带者率≥0.5%,其中大多数与遗传性代谢疾病相关。基因携带者率较高且高频变异的值得关注的基因包括:c.235del、c.728G>A,、c.2333G>T、c.919-2A>G、c.1901T>C、c.2890C>T、c.1472C>G、c.2802T>G、c.852_855del、c.761C>T和c.752C>T。本研究对我们实验室构建的ECS panel的216种疾病在中国人群中的携带频率和热点变异进行了重点分析,为制定适合中国人群的ECS计划奠定了基础。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验