Back

First-Trimester Non-Invasive Prediction of Preterm Birth Using Cell-Free DNA Fragmentomics

Pham, M.-D. N.; Phan, M.-T. T.; Tran, N.-T.; Vo, T.-S.; Le, H.-T.; Nguyen, T.-H. T.; Nguyen, Q.-H. V.; Ha, M.-T. T.; Le, T. M.; Hoang, D.-T. T.; Huynh, K.-T. N.; Nguyen, N. V.; Nguyen, C. C.; Bui, T. C.; Nguyen, X. T.; Le, S. V.; Tran, V. D.; Nguyen, M.-N. B.; Nguyen, T. V.; Nguyen, T.-A. T.; Hoang, B. P.; Nguyen, T. V.; Nguyen, T.-A. T.; Nguyen, T. T.; Duong, T. D.; Pham, C. H.; Luong, K.-O. T.; Dao, C. N.; Hoang, K. V.; Huynh, T.-T. T.; Nguyen, K. M.; Tran, S.-T. T.; Tran, H. T.; Nguyen, S. C.; Tran, T. D.; Nguyen, P. T. L.; Pham, T. V.; Pham, K. C.; Thai, M. D.; Do, T.-T. T.; Dao, H. T.; Va

2026-07-11 genomics
10.64898/2026.07.07.736241 bioRxiv
Show abstract

ObjectiveTo develop and validate a cell-free DNA (cfDNA) fragmentomic classifier for the early prediction of spontaneous preterm birth (PTB) using routine first-trimester non-invasive prenatal testing (NIPT) data. MethodsA nested case-control study was conducted within a prospective multicenter Vietnamese cohort comprising 286 pregnancies, including 82 spontaneous PTB cases and 204 term controls. Maternal plasma cfDNA collected during routine first-trimester NIPT (median gestational age, 12 weeks) was sequenced to a depth of approximately 20 million reads per sample. Five fragmentomic feature categories including copy number alterations, end-motif composition, nucleosome distance, fragment length, and joint fragment-lengthxend-motif were evaluated for PTB prediction. Machine learning classifiers were developed in a training cohort (n = 228, 65 PTB vs 163TB) and tested in a validation cohort (n = 58, 17 PTB vs 41 TB). ResultsAmong the five fragmentomic feature classes evaluated, 4-mer end-motif (EM) profiles exhibited the most pronounced differences between PTB and term control samples. Consistent with these findings, the EM-based classifier demonstrated the highest discriminative performance in the validation cohort, achieving an AUC of 0.970 (95% CI, 0.912-1.000). At a specificity >90%, the model achieved a sensitivity of 94% (95% CI, 78-100%). ConclusionThese findings demonstrate that cfDNA EM signatures derived from routine first-trimester NIPT can accurately identify pregnancies at risk of spontaneous preterm birth, without additional blood collection or sequencing, thereby extending the clinical utility of existing prenatal screening infrastructure. KEY POINTSO_ST_ABSWhat is already known about this topic?C_ST_ABSO_LICurrent first-trimester prediction strategies based on maternal characteristics, cervical length, and biochemical markers have limited predictive accuracy, particularly in nulliparous women. C_LIO_LIExisting cfDNA-based approaches have shown only modest performance or require additional assays, limiting clinical applicability. C_LI What does this study add?O_LIExisting NIPT sequencing data can be repurposed (without additional blood sampling or sequencing) for accurate prediction of spontaneous preterm birth (AUC=0.970). C_LIO_LIA classifier employing 4-mer end-motif (EM) profiles achieved an AUC of 0.970. At a specificity >90%, the model achieved a sensitivity of 94%. C_LI

Matching journals

The top 14 journals account for 50% of the predicted probability mass.

1
PLOS ONE
5266 papers in training set
Top 14%
13.2%
2
Scientific Reports
3612 papers in training set
Top 8%
7.7%
3
BMC Medical Genomics
50 papers in training set
Top 0.1%
5.5%
4
BioData Mining
22 papers in training set
Top 0.1%
3.4%
5
BMC Genomics
406 papers in training set
Top 2%
3.3%
6
Genetics in Medicine
78 papers in training set
Top 0.5%
2.5%
7
Journal of Clinical Medicine
97 papers in training set
Top 2%
2.1%
8
Nature Communications
5641 papers in training set
Top 42%
2.1%
9
Placenta
22 papers in training set
Top 0.2%
1.8%
10
Genes
144 papers in training set
Top 2%
1.8%
11
BMC Pregnancy and Childbirth
21 papers in training set
Top 0.4%
1.8%
12
Diagnostics
50 papers in training set
Top 1%
1.8%
13
Human Molecular Genetics
141 papers in training set
Top 1%
1.8%
14
Frontiers in Genetics
230 papers in training set
Top 3%
1.6%
50% of probability mass above
15
The Pharmacogenomics Journal
11 papers in training set
Top 0.1%
1.6%
16
Wellcome Open Research
67 papers in training set
Top 0.8%
1.5%
17
Journal of Clinical Virology
63 papers in training set
Top 0.5%
1.4%
18
Clinical Infectious Diseases
235 papers in training set
Top 2%
1.2%
19
GigaScience
212 papers in training set
Top 3%
1.2%
20
eBioMedicine
183 papers in training set
Top 4%
1.2%
21
PLOS Global Public Health
344 papers in training set
Top 6%
1.2%
22
Communications Medicine
113 papers in training set
Top 3%
1.2%
23
Journal of the American Heart Association
140 papers in training set
Top 3%
1.1%
24
The Journal of Nutrition
25 papers in training set
Top 0.4%
1.1%
25
JAMA Network Open
130 papers in training set
Top 3%
1.0%
26
European Journal of Human Genetics
58 papers in training set
Top 1.0%
1.0%
27
International Journal of Epidemiology
88 papers in training set
Top 2%
1.0%
28
Open Forum Infectious Diseases
142 papers in training set
Top 3%
0.9%
29
Frontiers in Pediatrics
32 papers in training set
Top 0.9%
0.9%
30
BioMed Research International
28 papers in training set
Top 2%
0.6%