Evidence map›Paper›PMID 41329681›Full record

ArticlePloS one2025

Targeted fetal NGS panel reveals genetic conditions in sonographically normal fetuses: Insights from a large cohort study.

Han-Ying Chen, Yi-Ting Wang, Jessica Kang, Yi-Yun Tai, Ti-Jia Yuan, Shin-Yu Lin, Shi-Ming Lin, Chien-Nan Lee, Tsang-Ming Ko

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Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Han-Ying ChenProgram for Precision Health and Intelligent Medicine, Graduate School of Advanced Technology, National Taiwan University, Taipei, Taiwan.ORCID https://orcid.org/0000-0001-9358-9210
Yi-Ting WangInstitute of Molecular Medicine Genetic Counseling Program, College of Medicine, National Taiwan University, Taipei, Taiwan.
Jessica KangDepartment of Obstetrics and Gynecology, National Taiwan University Hospital, Taipei, Taiwan.
Yi-Yun TaiProgram for Precision Health and Intelligent Medicine, Graduate School of Advanced Technology, National Taiwan University, Taipei, Taiwan.
Ti-Jia YuanDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Shin-Yu LinDepartment of Obstetrics and Gynecology, National Taiwan University Hospital, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-0753-2793
Shi-Ming LinProgram for Precision Health and Intelligent Medicine, Graduate School of Advanced Technology, National Taiwan University, Taipei, Taiwan.
Chien-Nan LeeDepartment of Obstetrics and Gynecology, National Taiwan University Hospital, Taipei, Taiwan.
Tsang-Ming KoGenephile Bioscience Laboratory, Ko's Obstetrics and Gynecology, Taipei, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prenatal genetic testing plays a crucial role in prenatal diagnosis and is traditionally performed when abnormalities are detected on fetal ultrasound. With the widespread availability of next-generation sequencing (NGS), genetic screening is increasingly being applied to fetuses with normal ultrasound findings. This study aimed to evaluate the diagnostic yield and outcomes of NGS panel testing in a large cohort of pregnant women with sonographically normal fetuses. A retrospective analysis was conducted on 1,820 sonographically normal fetuses that underwent fetal NGS-targeted panel testing based on parental requests between June 2021 and June 2023. Among the 1,820 cases analyzed, no pathogenic mutations were identified in 833 (45.8%), 893 (49.1%) had an abnormal carrier status, and 94 (5.2%) exhibited pathogenic conditions, including 25 autosomal dominant, 29 autosomal recessive, 39 X-linked (35 hemizygous glucose-6-phosphate dehydrogenase [G6PD] cases), and one mitochondrial disorder. The most common autosomal recessive mutation was a homozygous pathogenic variant of GJB2 (19 cases). Furthermore, 48 patients carried heterozygous G6PD mutations, and 344 patients were identified as carriers of GJB2 variants. Other notable findings included 15 cases of familial hypercholesterolemia, five cases of Noonan syndrome, and two cases of osteogenesis imperfecta. The rare disorders identified were Wilson's disease, cystic fibrosis, Cockayne syndrome, and ototoxic hearing loss, all of which were observed in a single case. A fetal NGS-targeted panel yielded critical findings in 5.16% of sonographically normal fetuses, emphasizing its potential use in prenatal diagnosis. Effective screening requires careful variant selection and detailed pre- and post-test genetic counseling to ensure the clinical relevance and informed decision-making of parents.

Indexed as

FetusGenetic TestingHigh-Throughput Nucleotide SequencingPrenatal DiagnosisUltrasonography, PrenatalAdultCohort StudiesConnexin 26FemaleHumansMutationPregnancyRetrospective StudiesConnexin 26GJB2 protein, human

Identifiers

PMID41329681
PMCPMC12671786

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