Evidence map›Paper›PMID 42751469›Full record

ArticleGeburtshilfe und Frauenheilkunde2026

Maternal Malignancies Identified Through Non-invasive Prenatal Testing: A Systematic Review and Meta-Analysis.

Eduardo Teixeira, Gustavo Yano Callado, Daryane Rezzuto, Carolina Josué Vilella Waideman Puga, Henrique Provinciatto, Antonio Braga, Gabriele Tonni, Edward Araujo Júnior

Abstract read
In one paragraph

Article in Geburtshilfe und Frauenheilkunde, 2026. 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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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Eduardo TeixeiraDepartment of MedicineUniversity of Vassouras (Univassouras)VassourasRJBrazil.ORCID 0000-0002-3004-1087
Gustavo Yano CalladoFaculdade Israelita de Ciências da Saúde Albert EinsteinHospital Israelita Albert EinsteinSão PauloSPBrazil.ORCID 0000-0001-6694-6569
Daryane RezzutoDepartment of MedicineAmazonas State University (UEA)ManausAMBrazil.ORCID 0009-0001-5827-9927
Carolina Josué Vilella Waideman PugaDepartment of MedicineThe City University of São Paulo (UNICID)São PauloSPBrazil.ORCID 0009-0001-9744-7268
Henrique ProvinciattoDepartment of MedicineBarão de Maua University CenterRibeirão PretoSPBrazil.ORCID 0009-0007-6376-0305
Antonio BragaDepartment of MedicineUniversity of Vassouras (Univassouras)VassourasRJBrazil.ORCID 0000-0002-2942-6182
Gabriele TonniPrenatal Diagnostic Center, Department of Obstetrics and NeonatologyIstituto di Ricovero e Cura a Carattere Scientifico (IRCCS), AUSL Reggio EmiliaReggio EmiliaItaly.ORCID 0000-0002-2620-7486
Edward Araujo JúniorDepartment of ObstetricsPaulista School of Medicine - Federal University of São Paulo (EPM-UNIFESP)São PauloSPBrazil.ORCID 0000-0002-6145-2532

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Non-invasive prenatal testing (NIPT) may incidentally reveal chromosomal abnormalities of maternal origin. Although specific chromosomal aberrations have been associated with maternal malignancy, reported risks vary widely. This meta-analysis aimed to quantify the magnitude and consistency of these associations. Methods: A systematic review and meta-analysis of observational studies reporting maternal malignancy among pregnant individuals with abnormal NIPT results was conducted. Odds ratios (ORs) with 95% confidence intervals (CIs) were pooled using a random-effects model. Risk of bias was assessed using the ROBINS-I tool. Results: Six studies met the inclusion criteria. Multiple chromosomal aberrations (MCA), although representing a minority of abnormal NIPT findings, accounted for a substantial proportion of confirmed maternal malignancies. MCA were strongly associated with cancer (OR 239.98; 95% CI 80.16-718.44; I Conclusion: Multiple chromosomal aberrations and complex gain-loss patterns on NIPT were strongly associated with maternal malignancy. These findings support the use of structured diagnostic pathways and targeted clinical evaluation when high-risk genomic patterns are identified.

Indexed as

cell-free DNAchromosomal aberrationscopy-number variationgenome-wide NIPTmaternal malignancynon-invasive prenatal testingprenatal screening

Identifiers

PMID42751469
PMCPMC13581417

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.