Hao Chanjuan, Hu Xuyun, Guo Ruolan, Qi Zhan, Jin Feng, Zhang Xiaofen, Xie Limin, Liu Haihong, Liu Yuanhu, Ni Xin, Li Wei
Beijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute; MOE Key Laboratory of Major Diseases in Children; Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Henan Key Laboratory of Inherited Metabolic Diseases, Pediatric Research Institute of Zhengzhou Children's Hospital, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, Henan, China.
Eur J Hum Genet. 2025 Apr;33(4):468-475. doi: 10.1038/s41431-024-01711-x. Epub 2024 Oct 23.
Hearing loss is a common congenital condition. Concurrent newborn hearing and limited genetic screening has been implemented in China for the last decade. However, the role of gene sequencing screening has not been evaluated. In this study, we enrolled 7501 newborns (52.7% male, 47.3% female) in our Newborn Screening with Targeted Sequencing (NESTS) program, and 90 common deafness genes were sequenced for them. Hearing status assessments were conducted via telephone from February 2021 to August 2022, for children aged 3 to 48 months. Of the universal newborn hearing screening, 126 (1.7%) newborns did not pass. Targeted sequencing identified 150 genetically positive newborns (2.0%), with 25 exhibiting dual-positive results in both screening. Following diagnostic audiometry revealed 18 hearing loss newborns and half of them had abnormal results in both screening. The positive predictive value for universal newborn hearing screening alone was merely 14.3% (18/126). However, when combined with targeted sequencing, this rate increased to 36.0% (9/25). Furthermore, limited genetic screening identified 316 carriers of hot-spot variants, but none exhibited biallelic variants. All 15 hot-spot carriers who failed physical screening demonstrated normal hearing during follow-up. In this cohort study of 7501 Newborns, Combining targeted sequencing with universal newborn hearing screening demonstrated technical feasibility and clinical utility of identifying individuals with hearing loss, especially when coupled with genetic counseling and closed-loop management. It is suggested to use this integrated method as an improved strategy instead of the current limited genetic screening program in some regions of China.
听力损失是一种常见的先天性疾病。在过去十年中,中国已实施了新生儿听力同步和有限的基因筛查。然而,基因测序筛查的作用尚未得到评估。在本研究中,我们将7501名新生儿(52.7%为男性,47.3%为女性)纳入我们的靶向测序新生儿筛查(NESTS)项目,并对他们进行了90个常见耳聋基因的测序。在2021年2月至2022年8月期间,通过电话对3至48个月大的儿童进行了听力状况评估。在普遍的新生儿听力筛查中,有126名(1.7%)新生儿未通过。靶向测序确定了150名基因检测呈阳性的新生儿(2.0%),其中25名在两项筛查中均呈双阳性结果。后续诊断性听力测试发现18名听力损失新生儿,其中一半在两项筛查中结果均异常。仅普遍新生儿听力筛查的阳性预测值仅为14.3%(18/126)。然而,当与靶向测序相结合时,这一比例增至36.0%(9/25)。此外,有限的基因筛查确定了316名热点变异携带者,但没有发现双等位基因变异。所有15名未通过体格筛查的热点变异携带者在随访期间听力均正常。在这项对7501名新生儿的队列研究中,将靶向测序与普遍新生儿听力筛查相结合证明了识别听力损失个体的技术可行性和临床实用性,特别是在结合遗传咨询和闭环管理时。建议在中国一些地区使用这种综合方法作为一种改进策略,以取代当前有限的基因筛查项目。