Prenatal Cell-free DNA Screening in Pregnancies With Diverse Genetic Risk Profiles Utilizing Targeted and Whole-exome Sequencing

Overview

This multicenter study aims to recruit a minimum of 1,600 pregnant women, encompassing individuals with varying levels of genetic risk. The study particularly focuses on cases with increased fetal nuchal translucency (NT ≥3.5 mm), additional ultrasound markers, and/or fetal structural anomalies. Peripheral blood samples of eligible participants will be collected for two state-of-the-art cfDNA tests based on coordinative allele-aware target enrichment sequencing (COATE-seq): (1) a targeted panel to screen for frequent chromosomal aneuploidies, microdeletions/duplications, and dominant single-gene conditions, and (2) comprehensive whole-exome cfDNA sequencing for aneuploidies, microdeletions/duplications, monogenic variants (both dominant and recessive variants), uniparental disomy, and hydatidiform moles. The results of both cfDNA tests will be compared with those from invasive or postnatal diagnostic testing. Pregnancy outcome will be followed up to six weeks postpartum. The primary goal is to determine the clinical validity of targeted and whole exome cfDNA analyses, assessed through sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) relative to diagnostic standards. Secondary goal is to assess efficacy across diverse genetic risk populations by analyzing detection rates of pathogenic variants associated with fetal indications. The clinical utility of cfDNA screening will also be evaluated by its impact on clinical management decisions, including follow-up diagnostic procedures or prenatal/perinatal interventions.

This prospective, multicenter clinical study is designed to evaluate the clinical validity and utility of a novel non-invasive prenatal screening platform, COATE-seq (Coordinative Allele-Aware Target Enrichment Sequencing). The study assesses the performance of cfDNA-based testing that integrates both targeted panel and whole-exome sequencing (WES) approaches to detect a broad range of fetal genetic abnormalities-including aneuploidies, microdeletions, monogenic pathogenic variants, uniparental disomy (UPD), and hydatidiform moles from a single maternal blood sample. The overarching aim is to establish the diagnostic accuracy, clinical effectiveness, and real-world impact of this comprehensive assay in routine prenatal care settings. The primary objective is to evaluate test performance through standard metrics including sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV), benchmarked against confirmatory diagnostic results. The secondary objectives focus on comparing detection rates across genetic risk subgroups (e.g., structural anomalies on ultrasound), quantifying the incremental yield of WES over targeted panels, and assessing clinical impact on management decisions. These endpoints are particularly relevant in an era of expanding therapeutic options for genetic conditions where early, non-invasive detection may significantly influence prenatal or perinatal interventions. Participants will be pregnant women between 9+0 and 25+6 weeks of gestation with singleton pregnancies who meet the following inclusion criteria: Age 18 years or older; Willingness to provide informed consent and participate in all study procedures; Presence of fetal findings on ultrasound meeting one of the following: Increased nuchal translucency (NT ≥3.5 mm), with or without additional markers; Structural anomalies detected on prenatal imaging; Agreement to undergo at least one molecular diagnostic test (prenatal or postnatal), and possible follow-up testing in family members. Exclusion criteria include: Gestational age outside of 9+0 to 25+6 weeks; Age under 18 years; Presence of a known familial pathogenic variant fully explaining the fetal ultrasound findings; Maternal conditions that may confound cfDNA analysis, such as active malignancy, recent allogeneic blood transfusion, organ transplantation, or cell-based therapy within the past year. The initial visit includes informed consent, demographic and clinical history collection, fetal ultrasound evaluation, and sample collection for cfDNA analysis and diagnostic testing (if available). The cfDNA assay incorporates targeted and exome-based sequencing of fetal DNA fragments isolated from maternal plasma. The second visit is an interim follow-up for review of diagnostic results and patient counseling. The final visit involves pregnancy outcome documentation via chart review or direct follow-up, capturing live birth, miscarriage, stillbirth, or elective termination, and any available postnatal phenotype confirmation. The COATE-seq assay uses hybrid-capture-based NGS to detect chromosomal aneuploidies (e.g., T21, T18, T13), pathogenic microdeletions (e.g., 22q11.2 deletion syndrome), and a curated panel of 56 monogenic conditions selected through the SEPH framework prioritizing severe, early-onset, prevalent, and analytically detectable disorders. The complementary WES component targets \~19,000 genes to broaden detection beyond predefined panels and support exploratory analysis of novel or rare variants. Variant interpretation adheres to ACMG guidelines, and only pathogenic or likely pathogenic variants associated with serious outcomes are reported. All cfDNA results are compared against one or more reference diagnostic methods, including karyotyping, chromosomal microarray (CMA), targeted gene panels, WES, and whole-genome sequencing. In selected cases, UPD is confirmed via methylation-specific testing or STR profiling. Performance metrics will be calculated on subjects with completed cfDNA and diagnostic data, and efficacy analyses will examine detection rates by condition type and risk strata. Quality assurance measures are built into all stages of the protocol, from sample collection and transport to bioinformatic analysis and reporting. This study complies with Good Clinical Practice (GCP) and all relevant ethical regulations. Institutional Review Board (IRB) approval is required at each participating site, and informed consent is obtained prior to any study procedures. Confidentiality of subject data is strictly maintained, and adverse events including complications from invasive diagnostic procedures. The study's findings will be disseminated via scientific publications and presentations, contributing to the evidence base for expanded cfDNA screening in prenatal care.