Evidence map›Paper›PMID 34723679›Full record

ArticleScience progress2021

A multivariate modeling method for the prediction of low fetal fraction before noninvasive prenatal testing.

Liang Hu, Yuanyuan Pei, Xiaojin Luo, Lijuan Wen, Hui Xiao, Jinxing Liu, Liping Wu, Gaochi Li, Fengxiang Wei

Open access · diamondAbstract read
In one paragraph

Article in Science progress, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact, top 82% of its field
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. PAPPA's role in female reproduction.Reproduction (Cambridge, England) · 2025
    Review
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

9 authors at 3 institutions in 1 country.

Liang HuCentral Laboratory, Longgang District Maternity & Child Healthcare Hospital of Shenzhen City, Shenzhen, China.
Yuanyuan PeiCentral Laboratory, Longgang District Maternity & Child Healthcare Hospital of Shenzhen City, Shenzhen, China.
Xiaojin LuoCentral Laboratory, Longgang District Maternity & Child Healthcare Hospital of Shenzhen City, Shenzhen, China.
Lijuan WenCentral Laboratory, Longgang District Maternity & Child Healthcare Hospital of Shenzhen City, Shenzhen, China.
Hui XiaoDepartment of Pathology, Shenzhen Longgang People's Hospital, Shenzhen, China.
Jinxing LiuCentral Laboratory, Longgang District Maternity & Child Healthcare Hospital of Shenzhen City, Shenzhen, China.
Liping WuPrenatal Diagnosis Center, Longgang District Maternity & Child Healthcare Hospital of Shenzhen City, Shenzhen, China.
Gaochi LiCentral Laboratory, Longgang District Maternity & Child Healthcare Hospital of Shenzhen City, Shenzhen, China.
Fengxiang WeiCentral Laboratory, Longgang District Maternity & Child Healthcare Hospital of Shenzhen City, Shenzhen, China.ORCID 0000-0001-7559-2504
Shenzhen Maternity and Child Healthcare Hospital · CNLonggang Central Hospital · CNZunyi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate factors associated with fetal fraction and to develop a new predictive method for low fetal fraction before noninvasive prenatal testing.

methodsThe study was a retrospective cohort analysis based on the results of noninvasive prenatal testing, complete blood count, thyroxin test, and Down's syndrome screening during the first or second trimester in 14,043 pregnant women. Random forests algorithm was applied to predict the low fetal fraction status (fetal fraction < 4%) through individual information and laboratory records. The performance of the model was evaluated and compared to predictions using maternal weight.

resultsOf 14,043 cases, maternal weight, red blood cell, hemoglobin, and free T3 were significantly negatively correlated with fetal fraction while gestation age, free T4, pregnancy-associated plasma protein-A, alpha-fetoprotein, unconjugated estriol, and β-human chorionic gonadotropin were significantly positively correlated with fetal fraction. Compared to predictions using maternal weight as an isolated parameter, the model had a higher area under the curve of receiver operating characteristic and overall accuracy.

conclusionsThe comprehensive predictive method based on combined multiple factors was more effective than a single-factor model in low fetal fraction status prediction. This method can provide more pretest quality control for noninvasive prenatal testing.

Indexed as

Down SyndromeNoninvasive Prenatal TestingChorionic Gonadotropin, beta Subunit, HumanFemaleHumansPregnancyPregnancy-Associated Plasma Protein-ARetrospective StudiesChorionic Gonadotropin, beta Subunit, HumanPregnancy-Associated Plasma Protein-AFetal fractionnoninvasive prenatal testingprediction modelprenatal screeningrandom forests

Identifiers

PMID34723679
PMCPMC10358597
OpenAlexW3208551941

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.