Evidence map›Paper›PMID 39208873›Full record

ArticleAmerican journal of perinatology2025

The Effect of Self-Reported Race on Noninvasive Prenatal Screening Test Characteristics.

Anjali N Mitra, Aleksei Dingel, Teodora Kolarova, Hayley J MacKinnon, Ronit Katz, Christina M Lockwood, Raj Shree

Abstract read
In one paragraph

Article in American journal of perinatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

7 authors.

Anjali N MitraDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington.ORCID 0000-0003-1787-8170
Aleksei DingelSchool of Medicine, University of Washington, Seattle, Washington.
Teodora KolarovaDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington.
Hayley J MacKinnonDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington.
Ronit KatzDepartment of Obstetrics and Gynecology, University of Washington, Seattle, Washington.
Christina M LockwoodDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington.
Raj ShreeDivision of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington.

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
NRSA Training CoreTL1TR002318 · NCATS · UNIVERSITY OF WASHINGTON · PI Megan Moore · 2017 to 2026
$8.4M
Cardiovascular disease, preeclampsia, and microchimerismK08HL150169 · NHLBI · UNIVERSITY OF WASHINGTON · PI SHREE, RAJ · 2020 to 2024
$816k
NCATS NIH HHS TL1 TR002318NCATS NIH HHS UL1 TR002319NHLBI NIH HHS K08 HL150169
6 · The paper itself

Abstract

objectiveLow fetal fraction (FF) on cell-free DNA (cfDNA)-based noninvasive prenatal screening (NIPS) is a common etiology for indeterminate results. As maternal Black race is implicated as a risk factor for low FF and more indeterminate results, we sought to evaluate this association. STUDY

designThis was a single-institution, retrospective cohort study of cfDNA-based NIPS performed between May 2017 and May 2022 with complete clinical data abstraction. We compared FF, indeterminate rates, and total cfDNA concentration among self-reported Black, White, and Other groups from NIPS results from 2017 to 2022 with full clinical data abstraction. Using linear regression and interaction testing, we evaluated associations between self-reported race, FF, indeterminate rate, and total cfDNA concentration.

resultsIn total, 1,591 participants met the inclusion criteria; 70.8% (

conclusionIn our population, maternal self-identified race, particularly Black race, does not affect FF. Biological plausibility for race-based differences on clinical tests requires ongoing thoughtful consideration. KEY POINTS: · NIPS is widely used to screen for fetal aneuploidy.. · FF is an important test metric, and low FF is associated with adverse outcomes, like aneuploidy.. · In existing studies, Black race is implicated as a risk factor for lower FF.. · Our study found no differences in FF between groups by self-reported race.. · Biological plausibility for race-based differences on clinical tests requires ongoing consideration..

Indexed as

Cell-Free Nucleic AcidsNoninvasive Prenatal TestingSelf ReportAdultBlack or African AmericanFemaleHumansPregnancyRetrospective StudiesWhiteCell-Free Nucleic Acids

Identifiers

PMID39208873
PMCPMC12404153

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Registered trials

None linked

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.