Evidence map›Paper›PMID 30606146›Full record

ArticleBMC pediatrics2019

Ontogeny of alkaline phosphatase activity in infant intestines and breast milk.

Ye Yang, Emilee Rader, Michele Peters-Carr, Rebecca C Bent, Jennifer T Smilowitz, Karen Guillemin, Bethany Rader

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC pediatrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01817127 (Functional Deconstruction of Human Milk Oligosaccharides and Lipids), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 15% 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.

NCT01817127 active not recruitingnot on this map

Functional Deconstruction of Human Milk Oligosaccharides and Lipids

TypeobservationalSponsorUniversity of California, DavisRan2009 to 2028Enrolled395ConditionsHealthy, Gestational Diabetes Mellitus, Type 2 Diabetes Mellitus
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. A Framework for Evaluation of New Processing Technologies in Human Milk Banking.Comprehensive reviews in food science and food safety · 2025
    Review
  2. Article
  3. Article
  4. Review
  5. [Yerba mate as a safe polyphenolic source during human lactation].Revista medica del Instituto Mexicano del Seguro Social · 2022
    Article
  6. Review
  7. Observational
  8. Article
  9. Article
  10. Review
  11. Article
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 at 6 institutions in 1 country.

Ye YangInstitute of Molecular Biology, University of Oregon, Eugene, OR, USA.
Emilee RaderDepartment of Media and Information, Michigan State University, East Lansing, MI, USA.
Michele Peters-CarrPeaceHealth Nurse Midwifery Birth Center, Springfield, OR, USA.
Rebecca C BentNeonatal Intensive Care Unit, RiverBend Medical Center, Springfield, OR, USA.
Jennifer T SmilowitzFoods for Health Institute, University of California at Davis, Davis, CA, USA.
Karen GuilleminInstitute of Molecular Biology, University of Oregon, Eugene, OR, USA.
Bethany RaderDepartment of Microbiology, Southern Illinois University, Life Science II Room 131, 1125 Lincoln Drive, Carbondale, IL, 62901, USA. bethany.rader@siu.edu.ORCID 0000-0001-8709-7244
University of Oregon · USMichigan State University · USPeaceHealth St. John Medical Center · USSacred Heart Medical Center at RiverBend · USSouthern Illinois University Carbondale · USUniversity of California, Davis · US

Funding

Research Area IIIP50GM098911 · NIGMS · UNIVERSITY OF OREGON · PI CONERY, JOHN · 2012 to 2016
$9.8M
Necrotizing Enterocolitis: Prevention and PredictionR01HD059127 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEBRILLA, CARLITO B, MILLS, DAVID ANDREW · 2008 to 2012
$3.1M
Structures, Functions, & Genetic Diversity of Oligosaccharides in MilkR01HD061923 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEBRILLA, CARLITO B · 2009 to 2013
$1.6M
Molecular and genetic analysis of the hielcobacter pylori virulence Factor CagAR01DK075667 · NIDDK · UNIVERSITY OF OREGON · PI GUILLEMIN, KAREN J · 2007 to 2010
$1.1M
NICHD NIH HHS R01 HD059127NICHD NIH HHS R01 HD061923NIDDK NIH HHS R01 DK075667NIGMS NIH HHS P50 GM098911
6 · The paper itself

Abstract

backgroundNecrotizing enterocolitis (NEC) is a devastating disease of intestinal inflammation that primarily affects premature infants. A potential risk factor for necrotizing enterocolitis is exposure of the premature neonatal intestine to environmental bacteria and their proinflammatory products such as lipopolysaccharide. The metalloenzyme alkaline phosphatase (ALP) has been shown to reduce lipopolysaccharide-mediated inflammation. Additionally, premature rat pups have reduced alkaline phosphatase activity and expression as compared to full term pups. To explore the possibility that the human premature neonatal intestine has a paucity of alkaline phosphatase activity, we measured endogenously produced intestinal alkaline phosphatase activity in meconium as a function of gestational age. To test whether breast milk could serve as a source of exogenous alkaline phosphatase to the neonatal intestine through ingestion, we measured alkaline phosphatase activity in breast milk across a range of time points post-birth.

methodsAlkaline phosphatase activity was quantified in 122 meconium samples from infants of gestational ages ranging from 24 to 40 weeks and in 289 breast milk samples collected from 78 individual mothers between days 2-49 post-birth.

resultsWe observed a strong positive correlation between the meconium alkaline phosphatase activity and gestational age, with preterm infants having lower meconium alkaline phosphatase activities than early term or term infants. Breast milk alkaline phosphatase activity was highest in the first week post-birth, with peak alkaline phosphatase activity at day 2 post-birth, followed by relatively low alkaline phosphatase activity in weeks 2-7.

conclusionsOur results are consistent with the two major risk factors for necrotizing enterocolitis development, preterm birth and lack of breast milk feeding, both contributing to a paucity of alkaline phosphatase activity and impaired capacity to detoxify proinflammatory bacterial products such as lipopolysaccharide.

Indexed as

Alkaline PhosphataseEnterocolitis, NecrotizingGestational AgeHumansInfantInfant, NewbornIntestinesMilk, HumanAlkaline PhosphataseGestational ageLPS detoxificationMeconiumNecrotizing enterocolitis (NEC)

Identifiers

PMID30606146
PMCPMC6318838
OpenAlexW2947563452

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.