Evidence map›Paper›PMID 27836286›Full record

ArticleThe Journal of pediatrics2017

Acylcarnitine Profiles Reflect Metabolic Vulnerability for Necrotizing Enterocolitis in Newborns Born Premature.

Karl G Sylvester, Zachary J Kastenberg, R Larry Moss, Gregory M Enns, Tina M Cowan, Gary M Shaw, David K Stevenson, Tiffany J Sinclair, Curt Scharfe, Kelli K Ryckman and 1 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

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  13. State-of-the-art review and update ofFrontiers in pediatrics · 2023
    Review
  14. Metabolic differences among newborns born to mothers with a history of leukemia or lymphoma.The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Karl G SylvesterDepartment of Surgery, Stanford University School of Medicine, Stanford, CA; Center for Fetal and Maternal Health, Lucile Packard Children's Hospital, Stanford, CA. Electronic address: Sylvester@Stanford.edu.
Zachary J KastenbergDepartment of Surgery, Stanford University School of Medicine, Stanford, CA; Center for Health Policy/Center for Primary Care and Outcomes Research, Stanford University/Stanford University School of Medicine, Stanford, CA.
R Larry MossPediatric Surgery, Nationwide Children's Hospital, Ohio State University School of Medicine, Columbus, OH.
Gregory M EnnsDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA.
Tina M CowanDepartment of Pathology, Stanford University School of Medicine, Stanford, CA.
Gary M ShawDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA.
David K StevensonDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA.
Tiffany J SinclairDepartment of Surgery, Stanford University School of Medicine, Stanford, CA.
Curt ScharfeStanford Genome Technology Center, Stanford University, Palo Alto, CA.
Kelli K RyckmanDepartments of Epidemiology and Pediatrics, College of Public Health and Carver College of Medicine, University of Iowa, Iowa, IA.
Laura L Jelliffe-PawlowskiDepartment of Epidemiology and Biostatistics, Division of Preventive Medicine and Public Health, University of California San Francisco School of Medicine, San Francisco, CA.
Stanford University · USNationwide Children's Hospital · USUniversity of California, San Francisco · USUniversity of Iowa · US

Funding

Stanford Center for Clinical and Translational Education and Research (SCCTER)UL1UL1RR025744 · NCRR · STANFORD UNIVERSITY · PI GREENBERG, HARRY BERNARD · 2008 to 2011
$22.4M
Training Program in Health Services ResearchT32HS000028 · AHRQ · STANFORD UNIVERSITY · PI OWENS, DOUGLAS K · 1986 to 2012
$1.6M
Qualifying Studies of Biomarkers for Neonatal DiseaseU01FD004194 · FDA · STANFORD UNIVERSITY · PI SYLVESTER, KARL G · 2011 to 2013
$915k
Technology development for rapid detection and diagnosis of metabolic disordersR01HD081355 · NICHD · YALE UNIVERSITY · PI SCHARFE, CURT · 2014 to 2016
$866k
Integrated Genomic and Metabolomic Profiles in Newborn InfantsR00HD065786 · NICHD · UNIVERSITY OF IOWA · PI RYCKMAN, KELLI K. · 2013 to 2015
$734k
AHRQ HHS T32 HS000028FDA HHS U01 FD004194NCRR NIH HHS UL1 RR025744NICHD NIH HHS R00 HD065786NICHD NIH HHS R01 HD081355
6 · The paper itself

Abstract

objectiveTo evaluate the association between newborn acylcarnitine profiles and the subsequent development of necrotizing enterocolitis (NEC) with the use of routinely collected newborn screening data in infants born preterm. STUDY

designA retrospective cohort study was conducted with the use of discharge records for infants born preterm admitted to neonatal intensive care units in California from 2005 to 2009 who had linked state newborn screening results. A model-development cohort of 94 110 preterm births from 2005 to 2008 was used to develop a risk-stratification model that was then applied to a validation cohort of 22 992 births from 2009.

resultsFourteen acylcarnitine levels and acylcarnitine ratios were associated with increased risk of developing NEC. Each log unit increase in C5 and free carnitine /(C16 + 18:1) was associated with a 78% and a 76% increased risk for developing NEC, respectively (OR 1.78, 95% CI 1.53-2.02, and OR 1.76, 95% CI 1.51-2.06). Six acylcarnitine levels, along with birth weight and total parenteral nutrition, identified 89.8% of newborns with NEC in the model-development cohort (area under the curve 0.898, 95% CI 0.889-0.907) and 90.8% of the newborns with NEC in the validation cohort (area under the curve 0.908, 95% CI 0.901-0.930).

conclusionsAbnormal fatty acid metabolism was associated with prematurity and the development of NEC. Metabolic profiling through newborn screening may serve as an objective biologic surrogate of risk for the development of disease and thus facilitate disease-prevention strategies.

Indexed as

Infant, PrematureBiomarkersCaliforniaCarnitineCohort StudiesConfidence IntervalsEnterocolitis, NecrotizingFemaleFollow-Up StudiesGestational AgeHumansIncidenceInfant, NewbornIntensive Care Units, NeonatalMaleMultivariate AnalysisacylcarnitineBiomarkersCarnitinefatty acidsmetabolismnewborn screenprematurity

Identifiers

PMID27836286
PMCPMC5538349
OpenAlexW2551474347

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.