Evidence map›Paper›PMID 26645954›Full record

ArticleAmerican journal of obstetrics and gynecology2016

Predicting gestational age using neonatal metabolic markers.

Kelli K Ryckman, Stanton L Berberich, John M Dagle

Open access · hybridAbstract read
In one paragraph

Article in American journal of obstetrics and gynecology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

38 citing papers in PubMed, 62 citations in OpenAlex.

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  12. Targeted newborn metabolomics: prediction of gestational age from cord blood.Journal of perinatology : official journal of the California Perinatal Association · 2022
    Article
  13. Gestational Age, Newborn Metabolic Markers and Academic Achievement.International journal of environmental research and public health · 2022
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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

3 authors at 1 institution in 1 country.

Kelli K RyckmanDepartment of Epidemiology, University of Iowa, Iowa City, IA; Department of Pediatrics, University of Iowa, Iowa City, IA. Electronic address: kelli-ryckman@uiowa.edu.
Stanton L BerberichState Hygienic Laboratory at the University of Iowa, Coralville, IA.
John M DagleDepartment of Pediatrics, University of Iowa, Iowa City, IA.
University of Iowa · US

Funding

Integrated Genomic and Metabolomic Profiles in Newborn InfantsR00HD065786 · NICHD · UNIVERSITY OF IOWA · PI RYCKMAN, KELLI K. · 2013 to 2015
$734k
NICHD NIH HHS R00 HD-065786NICHD NIH HHS R00 HD065786
6 · The paper itself

Abstract

backgroundAccurate gestational age estimation is extremely important for clinical care decisions of the newborn as well as for perinatal health research. Although prenatal ultrasound dating is one of the most accurate methods for estimating gestational age, it is not feasible in all settings. Identifying novel and accurate methods for gestational age estimation at birth is important, particularly for surveillance of preterm birth rates in areas without routine ultrasound dating.

objectiveWe hypothesized that metabolic and endocrine markers captured by routine newborn screening could improve gestational age estimation in the absence of prenatal ultrasound technology. STUDY

designThis is a retrospective analysis of 230,013 newborn metabolic screening records collected by the Iowa Newborn Screening Program between 2004 and 2009. The data were randomly split into a model-building dataset (n = 153,342) and a model-testing dataset (n = 76,671). We performed multiple linear regression modeling with gestational age, in weeks, as the outcome measure. We examined 44 metabolites, including biomarkers of amino acid and fatty acid metabolism, thyroid-stimulating hormone, and 17-hydroxyprogesterone. The coefficient of determination (R(2)) and the root-mean-square error were used to evaluate models in the model-building dataset that were then tested in the model-testing dataset.

resultsThe newborn metabolic regression model consisted of 88 parameters, including the intercept, 37 metabolite measures, 29 squared metabolite measures, and 21 cubed metabolite measures. This model explained 52.8% of the variation in gestational age in the model-testing dataset. Gestational age was predicted within 1 week for 78% of the individuals and within 2 weeks of gestation for 95% of the individuals. This model yielded an area under the curve of 0.899 (95% confidence interval 0.895-0.903) in differentiating those born preterm (<37 weeks) from those born term (≥37 weeks). In the subset of infants born small-for-gestational age, the average difference between gestational ages predicted by the newborn metabolic model and the recorded gestational age was 1.5 weeks. In contrast, the average difference between gestational ages predicted by the model including only newborn weight and the recorded gestational age was 1.9 weeks. The estimated prevalence of preterm birth <37 weeks' gestation in the subset of infants that were small for gestational age was 18.79% when the model including only newborn weight was used, over twice that of the actual prevalence of 9.20%. The newborn metabolic model underestimated the preterm birth prevalence at 6.94% but was closer to the prevalence based on the recorded gestational age than the model including only newborn weight.

conclusionsThe newborn metabolic profile, as derived from routine newborn screening markers, is an accurate method for estimating gestational age. In small-for-gestational age neonates, the newborn metabolic model predicts gestational age to a better degree than newborn weight alone. Newborn metabolic screening is a potentially effective method for population surveillance of preterm birth in the absence of prenatal ultrasound measurements or newborn weight.

Indexed as

Gestational AgeNeonatal Screening17-alpha-HydroxyprogesteroneAmino AcidsBiomarkersBirth WeightCarnitineFatty AcidsFemaleHumansInfant, NewbornLogistic ModelsMalePregnancyRetrospective StudiesThyrotropin17-alpha-HydroxyprogesteroneacylcarnitineAmino AcidsBiomarkersCarnitineFatty AcidsThyrotropinUTP-Hexose-1-Phosphate Uridylyltransferasefetal growthneonatal metabolismpreterm birth

Identifiers

PMID26645954
PMCPMC4808601
OpenAlexW2185989068

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.