Noninvasive prenatal diagnosis (NIPD) of non-syndromic hearing loss (NSHL) for singleton and twin pregnancies in the first trimester.

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2025-01-27 DOI:10.1186/s13023-025-03558-x
Huanyun Li, Shaojun Li, Zhenhua Zhao, Lingrong Kong, Xinyu Fu, Jingqi Zhu, Jun Feng, Weiqin Tang, Di Wu, Xiangdong Kong
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Abstract

Background: Noninvasive prenatal diagnosis (NIPD) has been proven feasible for non-syndromic hearing loss (NSHL) in singleton pregnancies. However, previous research is limited to the second trimester and the application in twin pregnancies is blank. Here we provide a novel algorithmic approach to assess singleton and twin pregnancies in the first trimester.

Methods: A 324.614 kb capture panel was designed to selectively enrich target regions. Parental haplotypes were constructed by target sequencing of blood samples from the parents and the proband. Then single nucleotide polymorphisms (SNP) within target regions were classified into four and six categories in singleton and twin pregnancy, respectively. Combining relative haplotype dosage change (RHDO) and the Bayes factor (BF), fetal fraction (FF) and fetal genotype were deduced in singleton and twin pregnancies. The pregnant women's NIPD results were validated by invasive prenatal diagnosis and Sanger sequencing.

Results: Sixteen women with singleton pregnancies and one woman with a twin pregnancy were recruited. Among the 16 singleton pregnancies, NIPD was successfully applied in 15 families and the coincidence rate with invasive prenatal diagnosis was 100% (15/15). Only one family NIPD result is "no call" because the imbalance distribution of SNP sites makes it difficult to estimate recombination events. Most (13/15) of pregnant women were diagnosed in the first trimester and the earliest gestation week was the 7th week. The twin pregnancy was a dichorionic diamniotic twin (DCDA). NIPD confirmed one fetus is affected, and another is a carrier with c.299_300delAT of GJB2 gene.

Conclusion: This study represents the pioneering evidence in the field, demonstrating the feasibility of NIPD for NSHL in twin pregnancies. Moreover, it provides a novel and advanced diagnostic approach for families at high risk of NSHL during pregnancy, offering earlier detection, enhanced safety, and improved accuracy.

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无创产前诊断(NIPD)的非综合征性听力损失(NSHL)的单胎和双胎妊娠在前三个月。
背景:无创产前诊断(NIPD)已被证明对单胎妊娠的非综合征性听力损失(NSHL)是可行的。然而,先前的研究仅限于妊娠中期,在双胎妊娠中的应用是空白的。在这里,我们提供了一种新的算法方法来评估单胎和双胎妊娠在前三个月。方法:设计一个324.614 kb的捕获面板,选择性地富集靶区。通过对父母和先证者的血液样本进行目标测序,构建亲本单倍型。将单胎妊娠和双胎妊娠的靶区单核苷酸多态性(SNP)分别分为4类和6类。结合相对单倍型剂量变化(RHDO)和贝叶斯因子(BF),推导出单胎和双胎妊娠的胎儿分数(FF)和胎儿基因型。通过有创产前诊断和Sanger测序验证孕妇NIPD结果。结果:16名单胎妊娠妇女和1名双胎妊娠妇女被招募。在16例单胎妊娠中,有15个家庭成功应用NIPD,与有创产前诊断符合率为100%(15/15)。只有一个家族的NIPD结果是“无效的”,因为SNP位点的不平衡分布使得难以估计重组事件。大多数(13/15)孕妇在妊娠早期被诊断,最早妊娠周为第7周。双绒毛膜双羊膜双胞胎(DCDA)。NIPD确认一名胎儿受到影响,另一名胎儿携带GJB2基因c.299_300delAT。结论:本研究代表了该领域的开创性证据,证明了NIPD治疗双胎妊娠NSHL的可行性。此外,它为妊娠期NSHL高风险家庭提供了一种新颖先进的诊断方法,提供了更早的检测,增强了安全性,提高了准确性。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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