Genetic rare disease prevention and control: Family-based screening and reproductive interventions in Changsha
Year: 2025
Type: article
Abstract: Rare diseases pose a significant public health challenge, particularly in underserved regions such as China, where genomic diagnostic services and post-diagnosis management remain limited. This study assessed the effectiveness of a rare disease screening program in Changsha, China, which enrolled 85,391 couples between January 2022 and June 2023. Among these participants were 1,414 suspected high-risk couples undergoing genetic testing, with 562 found to be at high risk of having a child with a rare disease, yielding a positive rate of 39.75%. Reproductive interventions were implemented for 319 families, successfully preventing rare disease-affected births in 141 cases. Diagnostic findings informed reproductive decision-making in 25.09% of cases and altered fertility plans in 32.74%. Machine learning analysis further revealed that participation in a parent-offspring trio and a positive family history significantly increased diagnostic likelihood, while singleton recruitment and a negative history were associated with lower diagnostic success. This pilot program highlights the value of integrating genetic diagnostics with reproductive interventions, offering a replicable model for rare disease prevention and management.
Authors: Ge Lin, Jun He, Yuankun Wang, Xiangyan Liu, Juan Du, Qianjun Zhang, Shihao Zhou, Lanping Hu, Jing He, Xiurong Li, Hao Hu, Liang Hu, Changgao Zhong, Wen-Bin He, Chan Peng, Zhen Xu, Jingjing Zhang, Yan Shu, Xuan Song, Wenqian Zhang, Guangxiu Lu, Zhiming Ou, Yue-Qiu Tan, Jiyang Liu
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,300
OpenAlex ID: W4413274428
