Department of Medical Genetics, Affiliated Shenzhen Maternity & Child Healthcare Hospital, Southern Medical University, Shenzhen, Guangdong, China.
Shenzhen Center for Chronic Disease Control, Shenzhen, Guangdong, China.
Mol Genet Genomic Med. 2024 Jan;12(1):e2359. doi: 10.1002/mgg3.2359.
To determine the carrier frequency of, and evaluate a carrier screening program for, spinal muscular atrophy (SMA) in reproductive age women in Shenzhen area.
A staged screening procedure was used to perform carrier screening for SMA in 22,913 Chinese reproductive age women between 2019 and 2022 in Shenzhen area of China. First, the copy number of exon 7 in the SMN1 gene were detected in women of reproductive age using real-time quantitative polymerase chain reaction. If SMA carriers were detected, their spouses were then recommended to test. Prenatal diagnosis was carried out in couples who were both carriers.
A total of 389 women were found to be SMA carriers (1.70%, 95% CI: 1.53%-1.87%), indicating the carrier prevalence was approximately 1:59. Despite the proportion of nonpregnant women increased from 37.96% in 2019 to 58.18% in 2022 (p < 0.05) among the 22,913 reproductive age women, the recall rate of spouses was still not high (62.21%, 95% CI: 57.39%-67.03%). Eight partners were found to be SMA carriers and two fetuses were determined to have SMA with no copies of the SMN1 gene.
Although the acceptability and awareness of SMA carrier screening in Chinese population has increased in recent years, it still fails to reach the ideal expectation. Our experience may provide a basis for and facilitate the popularization of SMA carrier screening in Shenzhen area.
确定深圳地区生育年龄女性脊髓性肌萎缩症(SMA)的携带率,并评估其携带者筛查计划。
采用分阶段筛查程序,对 2019 年至 2022 年期间深圳地区 22913 名生育年龄的中国女性进行 SMA 携带者筛查。首先,采用实时定量聚合酶链反应检测生育年龄女性 SMN1 基因外显子 7 的拷贝数。如果发现 SMA 携带者,则建议其配偶进行检测。对双方均为携带者的夫妇进行产前诊断。
共发现 389 名女性为 SMA 携带者(1.70%,95%置信区间:1.53%-1.87%),表明携带者患病率约为 1:59。尽管在 22913 名生育年龄女性中,非妊娠女性的比例从 2019 年的 37.96%增加到 2022 年的 58.18%(p<0.05),但配偶的召回率仍不高(62.21%,95%置信区间:57.39%-67.03%)。发现 8 名伴侣为 SMA 携带者,2 名胎儿无 SMN1 基因拷贝,被诊断为 SMA。
尽管近年来中国人群对 SMA 携带者筛查的可接受性和意识有所提高,但仍未达到理想预期。我们的经验可为深圳地区 SMA 携带者筛查的推广提供依据和便利。