# Clinical application of fetal Nuchal Translucency combined with noninvasive prenatal testing in screening chromosome abnormalities

**Authors:** Guangzhen Fu, Shuang Hu

PMC · DOI: 10.1371/journal.pone.0344739 · PLOS One · 2026-03-16

## TL;DR

This study shows that combining fetal nuchal translucency with noninvasive prenatal testing improves the detection of chromosomal abnormalities in early pregnancy.

## Contribution

The study demonstrates the clinical value of combining NT and NIPT for improved screening of fetal chromosomal abnormalities.

## Key findings

- Enlarged NT was significantly associated with a higher detection rate of chromosomal abnormalities.
- Most low-risk NIPT cases with enlarged NT resulted in healthy live births.
- The combination of NT and NIPT provides high predictive value for chromosomal abnormalities.

## Abstract

To explore the clinical application of fetal nuchal translucency (NT) combined with noninvasive prenatal testing (NIPT) in screening for fetal chromosomal diseases.

A retrospective analysis was performed on NIPT results, prenatal diagnoses, and pregnancy outcomes of early pregnant women with enlarged NT at our center from 01/07/2018 to 01/01/2021. To ensure data integrity and minimize extraction bias, phased data access was adopted: the first batch of data was extracted from 01/07/2019 (start of Phase 1) to 20/07/2019 (end of Phase 1), covering participants examined from 01/07/2018 to 30/06/2019; the second batch was extracted from 01/02/2020 (start of Phase 2) to 20/02/2020 (end of Phase 2), including participants examined from 01/07/2019 to 01/01/2020. Chi-square tests were used to compare the incidence of fetal chromosomal abnormalities between the enlarged NT and normal NT groups, as well as among the subgroups of enlarged NT.

Out of 48,130 women screened by NIPT, 774 had enlarged NT (≥2.5 mm); among these, 85 were classified as high-risk, and 72 underwent invasive diagnosis, resulting in 64 positive cases (including 42 cases of trisomy 21, among others). The thickening of NT was correlated with a higher detection rate of abnormalities, which was statistically significant. Among the 689 cases of enlarged NT with low-risk NIPT results, 20 were lost to follow-up, 5 terminated their pregnancies, while the others had healthy live births.

Early pregnancy NT combined with NIPT demonstrates a high predictive value for fetal chromosomal abnormalities and holds significant importance for clinical pregnancy guidance.

## Full-text entities

- **Diseases:** Chromosome (MESH:D025063), trisomies (MESH:D014314), Fetal chromosomal abnormalities (MESH:D005315), Chromosomal abnormalities (MESH:D002869), 21/18/13-trisomy (MESH:D000073839), Down syndrome (MESH:D004314), congenitally abnormal (MESH:D000013), congenital structural abnormalities (MESH:D020914), NT thickening (MESH:D013585), congenital heart defects (MESH:D006330), 18 trisomies (MESH:D000073842), enlarged NT (MESH:D006332), developmental disorders (MESH:D002658), NT (MESH:D053589), birth defects (MESH:D000014), abortion (MESH:D000026), aneuploidies (MESH:D000782), miscarriage (MESH:D000022), sex chromosome abnormalities (MESH:D012729)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12991258/full.md

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Source: https://tomesphere.com/paper/PMC12991258