在需要辅助生殖技术的种群中评估单源性疾病的载体频率
Xiuhua Xu1,2, Sijie He3, Gang Li4
1Department of Reproductive Medicine, Hebei Key Laboratory of Infertility and Genetics, Hebei Clinical Research Center for Birth Defects, Hebei Medical Key Discipline of Reproductive Medicine, Hebei Collaborative Innovation Center of Integrated Traditional and Western Medicine On Reproductive Disease, The Second Hospital of Hebei Medical University, Shijiazhuang, 050000, China.
BMC medical genomics
|August 19, 2024
概括
扩展载体查 (ECS) 显示,在接受辅助生殖的汉族人群中,严重的单一性衰退性疾病的载体率为44.74%. 这突出了ECS.
科学领域:
- 医学遗传学 医学遗传学
- 生殖医学 生殖医学
- 人口健康 人口健康
背景情况:
- 单源性衰退性疾病在生殖计划中构成重大风险.
- 扩展载体查 (ECS) 提供了一种全面的方法来识别遗传疾病的载体.
研究的目的:
- 确定155种严重的单一性衰退性疾病的载体频率和致病变异谱.
- 评估ECS在接受辅助生殖技术的汉族人口中的实用性.
主要方法:
- 使用ECS的155基因小组.
- 采用了下一代测序技术.
- 分析了来自河北省114个人 (97对夫妇) 的数据.
主要成果:
- 鉴定出致病基因携带率为44.74%.
- GJB2和MMACHC是最常见的基因,每个基因携带率为5.26%.
- 检测到55种变异,其中c.235delC是最常见的 (3.51%的载体率).
结论:
- 在评估生殖风险和预防先天性异常方面,ECS至关重要.
- 研究结果支持使用ECS来指导生育决策,并减少单一性疾病的发生率.
- 植入前遗传检测 (PGT) 和其他策略可以减轻夫妇共享突变时的风险.
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