Evidence map›Paper›PMID 31711265›Full record

ArticlePrenatal diagnosis2020

Cell-free DNA fetal fraction in twin gestations in single-nucleotide polymorphism-based noninvasive prenatal screening.

Herman Hedriana, Kimberly Martin, Daniel Saltzman, Paul Billings, Zachary Demko, Peter Benn

Abstract read
In one paragraph

Article in Prenatal diagnosis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Article
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  4. Observational
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  6. Cell-free DNA test for fetal chromosomal abnormalities in multiple pregnancies.Acta obstetricia et gynecologica Scandinavica · 2024
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  7. Article
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  9. Cell-free DNA screening in twin pregnancies.Obstetrics & gynecology science · 2024
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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

6 authors.

Herman HedrianaDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of California Davis Health, Sacramento, CA.ORCID 0000-0002-8656-5461
Kimberly MartinNatera, Inc, San Carlos, CA.ORCID 0000-0003-4077-1814
Daniel SaltzmanIcahn School of Medicine at Mount Sinai, New York, NY.
Paul BillingsNatera, Inc, San Carlos, CA.
Zachary DemkoNatera, Inc, San Carlos, CA.ORCID 0000-0001-8796-2381
Peter BennDepartment of Genetics and Genome Sciences, UConn Health, Farmington, CT.ORCID 0000-0001-7917-6946

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe performance of noninvasive prenatal screening (NIPS) for fetal aneuploidy in twin pregnancies is dependent on the amount of placentally derived cell-free DNA, the "fetal fraction (FF)," present in maternal plasma. We report FF values in monozygotic (MZ) and dizygotic (DZ) pregnancies.

methodsWe reviewed FF in pregnancies at 10 to 20 completed weeks gestational age based on single-nucleotide polymorphism (SNP)-based NIPS where zygosity was routinely established in twin pregnancies. The cohort included 121 446 (96.3%) singleton, 1454 (1.2%) MZ, and 3161 (2.5%) DZ pregnancies. For DZ twins, individual FFs were measured.

resultsCombined FF for DZ and MZ fetuses were 35% and 26% greater than singletons, respectively. The individual FF contributions from each fetus in DZ twins were, on average, 32% less than singletons. FF in DZ twin pairs were moderately correlated (Pearson correlation coefficient.66). When a threshold of 2.8% FF was applied to define uninterpretable results, 1.7% (2102/121 446) of singletons, 0.8% (11/1454) of MZ pairs, and 5.6% (178/3161) of DZ pairs were uninterpretable.

conclusionFor optimal aneuploidy NIPS in twin pregnancies, zygosity should be established and in DZ twins FF for both fetuses should be determined to identify those cases where results can be reliably interpreted.

Indexed as

AneuploidyTwins, DizygoticTwins, MonozygoticAdultCell-Free Nucleic AcidsFemaleHumansNoninvasive Prenatal TestingPregnancyPregnancy, TwinCell-Free Nucleic Acids

Identifiers

PMID31711265
PMCPMC7027570

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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.