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医学外显子组测序的临床应用:中国接受辅助生殖技术患者的扩展携带者筛查

Clinical Utility of Medical Exome Sequencing: Expanded Carrier Screening for Patients Seeking Assisted Reproductive Technology in China.

作者信息

Tong Keya, He Wenbin, He Yao, Li Xiurong, Hu Liang, Hu Hao, Lu Guangxiu, Lin Ge, Dong Chang, Zhang Victor Wei, Du Juan, Liu Dongyun

机构信息

Center for Reproductive Medicine, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.

Chongqing Key Laboratory of Human Embryo Engineering, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.

出版信息

Front Genet. 2022 Aug 22;13:943058. doi: 10.3389/fgene.2022.943058. eCollection 2022.

Abstract

Expanded carrier screening (ECS) is an effective method to identify at-risk couples (ARCs) and avoid birth defects. This study aimed to reveal the carrier spectrum in the Chinese population and to delineate an expanded carrier gene panel suitable in China. Medical exome sequencing (MES), including 4,158 disease-causing genes, was offered to couples at two reproductive centers. It was initially used as a diagnostic yield for potential patients and then used for ECS. Clinical information and ECS results were retrospectively collected. A total of 2,234 couples, representing 4,468 individuals, underwent MES. In total, 254 individuals showed genetic disease symptoms, and 56 of them were diagnosed with genetic diseases by MES. Overall, 94.5% of them were carriers of at least one disease-causing variant. The most prevalent genes were for autosomal recessive disorders and for X-linked diseases. The ARC rate was 9.80%, and couples were inclined to undergo preimplantation genetic testing when diseases were classified as "profound" or "severe." This study provided insight to establish a suitable ECS gene panel for the Chinese population. Disease severity significantly influenced reproductive decision-making. The results highlighted the importance of conducting ECS for couples before undergoing assisted reproductive technology.

摘要

扩展携带者筛查(ECS)是识别高危夫妇(ARCs)和避免出生缺陷的有效方法。本研究旨在揭示中国人群中的携带者谱,并划定适合中国的扩展携带者基因panel。两个生殖中心为夫妇提供了包含4158个致病基因的医学外显子测序(MES)。它最初用作潜在患者的诊断产出,然后用于ECS。回顾性收集临床信息和ECS结果。共有2234对夫妇(代表4468人)接受了MES。总共254人表现出遗传疾病症状,其中56人通过MES被诊断患有遗传疾病。总体而言,其中94.5%是至少一种致病变异的携带者。最常见的基因是常染色体隐性疾病相关基因和X连锁疾病相关基因。高危夫妇率为9.80%,当疾病被分类为“严重”或“极严重”时,夫妇倾向于接受植入前基因检测。本研究为建立适合中国人群的ECS基因panel提供了见解。疾病严重程度显著影响生殖决策。结果强调了在夫妇接受辅助生殖技术之前进行ECS的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1583/9441495/278d5ba3d5ee/fgene-13-943058-g001.jpg

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