Evidence map›Paper›PMID 23558011›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2013

Preterm human milk contains a large pool of latent TGF-β, which can be activated by exogenous neuraminidase.

Kopperuncholan Namachivayam, Cynthia L Blanco, Brandy L Frost, Aaron A Reeves, Ramasamy Jagadeeswaran, Krishnan MohanKumar, Azif Safarulla, Partha Mandal, Steven A Garzon, J Usha Raj and 1 more

Abstract readComparative Study
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

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  14. Transforming growth factor-β2 is sequestered in preterm human milk by chondroitin sulfate proteoglycans.American journal of physiology. Gastrointestinal and liver physiology · 2015
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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

11 authors at 3 institutions in 1 country.

Kopperuncholan NamachivayamDivision of Neonatology, Department of Pediatrics, University of Illinois at Chicago, Chicago, IL, USA.
Cynthia L Blanco
Brandy L Frost
Aaron A Reeves
Ramasamy Jagadeeswaran
Krishnan MohanKumar
Azif Safarulla
Partha Mandal
Steven A Garzon
J Usha Raj
Akhil Maheshwari
University of Illinois Chicago · USThe University of Texas Health Science Center at San Antonio · USUniversity of Chicago · US

Funding

INSTITUTE FOR INTEGRATION OF MEDICINE & SCIENCE: A PARTNERSHIP TO IMPROVE HEALTHUL1RR025767 · NCRR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A · 2008 to 2011
$23.8M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
Role of Transforming Growth Factor-beta in Neonatal Necrotizing EnterocolitisR01HD059142 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MAHESHWARI, AKHIL · 2009 to 2013
$1.7M
NCATS NIH HHS UL1 TR001120NCRR NIH HHS UL1 RR-025767NICHD NIH HHS R01 HD-059142NICHD NIH HHS R01 HD059142
6 · The paper itself

Abstract

Human milk contains substantial amounts of transforming growth factor (TGF)-β, particularly the isoform TGF-β2. We previously showed in preclinical models that enterally administered TGF-β2 can protect against necrotizing enterocolitis (NEC), an inflammatory bowel necrosis of premature infants. In this study we hypothesized that premature infants remain at higher risk of NEC than full-term infants, even when they receive their own mother's milk, because preterm human milk contains less bioactive TGF-β than full-term milk. Our objective was to compare TGF-β bioactivity in preterm vs. full-term milk and identify factors that activate milk-borne TGF-β. Mothers who delivered between 23 0/7 and 31 6/7 wk or at ≥37 wk of gestation provided milk samples at serial time points. TGF-β bioactivity and NF-κB signaling were measured using specific reporter cells and in murine intestinal tissue explants. TGF-β1, TGF-β2, TGF-β3, and various TGF-β activators were measured by real-time PCR, enzyme immunoassays, or established enzymatic activity assays. Preterm human milk showed minimal TGF-β bioactivity in the native state but contained a large pool of latent TGF-β. TGF-β2 was the predominant isoform of TGF-β in preterm milk. Using a combination of several in vitro and ex vivo models, we show that neuraminidase is a key regulator of TGF-β bioactivity in human milk. Finally, we show that addition of bacterial neuraminidase to preterm human milk increased TGF-β bioactivity. Preterm milk contains large quantities of TGF-β, but most of it is in an inactive state. Addition of neuraminidase can increase TGF-β bioactivity in preterm milk and enhance its anti-inflammatory effects.

Indexed as

AnimalsFemaleGene ExpressionHumansLactationMiceMilk, HumanNeuraminidaseNF-kappa BPremature BirthProtein IsoformsTerm BirthTime FactorsTransforming Growth Factor betaNeuraminidaseNF-kappa BProtein IsoformsTransforming Growth Factor betabreast milkinflammationnecrotizing enterocolitissialidasetransforming growth factor-β

Identifiers

PMID23558011
PMCPMC3680715
OpenAlexW2162784922

What OpenQuestion holds

Textmetadata
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.