Li Mengmeng, Hao Na, Chang Jiazhen, Yin Kaili, Yang Xueting, Wang Yaru, Dai Yi, Jiang Yulin
Department of Obstetrics, Peking Union Medical College Hospital, National Clinical Research Center for Obstetric & Gynecologic Diseases, Chinese Academy of Medical Science and Peking Union Medical College, No.1 Shuaifuyuan, Dongcheng District, Beijing, 100730, China.
Ecobono (Beijing) Biotech Co., Ltd, Beijing, China.
Orphanet J Rare Dis. 2025 Feb 11;20(1):67. doi: 10.1186/s13023-025-03591-w.
Facioscapulohumeral muscular dystrophy (FSHD) is the second most common form of muscular dystrophy, which is characterized by a reduction in the number of D4Z4 repeats on chromosome 4q35. Prenatal diagnosis of FSHD has been challenging due to the large quantity and high-quality DNA required for Southern blot (SB) analysis. Optical genome mapping (OGM) technology has shown promise in identifying repeat contraction disorders and presents a potential tool for the prenatal diagnosis of FSHD.
In this retrospective cohort study, we investigated the distribution of D4Z4 repeats in 100 unrelated healthy individuals from the Chinese Han population using peripheral blood samples and DLS labelling method. Additionally, prenatal diagnosis using OGM was performed in 12 FSHD families at Peking Union Medical College Hospital between January 2021 and December 2023. The prenatal samples included 2 amniotic cell cultures and 10 chorionic villus samples (CVS), with 9 labeled using DLS and 4 using NLRS method.
Among the 100 healthy controls, the distribution of D4Z4 repeats varied, with 3 individuals having borderline 10 repeat counts on 4qA, and the most frequent count being 14 units. One individual with mosaicism was also identified. In the cohort of 12 FSHD families,14 prenatal diagnoses were performed. Of these 14 cases, 4 fetuses tested positive for 4qA contraction, with repeat counts ranging from 2 to 4. In both families that underwent two rounds of prenatal diagnosis, the first diagnosis indicated the presence of FSHD, leading to pregnancy termination, while the second diagnosis confirmed the presence of healthy fetuses. The overall positive rate was 28.57%.
Our findings demonstrate that OGM is an accurate and effective method for the prenatal diagnosis of FSHD. The application of OGM in prenatal settings could offer significant benefits to families affected by FSHD with reproductive concerns.
面肩肱型肌营养不良症(FSHD)是第二常见的肌营养不良症形式,其特征是4号染色体长臂35区(4q35)上的D4Z4重复序列数量减少。由于Southern印迹(SB)分析需要大量高质量的DNA,FSHD的产前诊断一直具有挑战性。光学基因组图谱(OGM)技术在识别重复序列收缩障碍方面显示出前景,并为FSHD的产前诊断提供了一种潜在工具。
在这项回顾性队列研究中,我们使用外周血样本和DLS标记方法,调查了100名来自中国汉族人群的无亲缘关系健康个体中D4Z4重复序列的分布。此外,2021年1月至2023年12月期间,在北京协和医院对12个FSHD家庭进行了使用OGM的产前诊断。产前样本包括2份羊水细胞培养物和10份绒毛取样样本(CVS),其中9份使用DLS标记,4份使用NLRS方法标记。
在100名健康对照中,D4Z4重复序列的分布各不相同,3名个体在4qA上的重复计数处于临界值10,最常见的计数为14个单位。还鉴定出1名嵌合体个体。在12个FSHD家庭队列中,进行了14次产前诊断。在这14例病例中,4例胎儿4qA收缩检测呈阳性,重复计数范围为2至4。在接受两轮产前诊断的两个家庭中,首次诊断表明存在FSHD,导致终止妊娠,而第二次诊断证实胎儿健康。总体阳性率为28.57%。
我们的研究结果表明,OGM是FSHD产前诊断的一种准确有效的方法。OGM在产前环境中的应用可为受FSHD影响且有生殖担忧的家庭带来显著益处。