Evidence map›Paper›PMID 42060676›Full record

ArticlePloS one2026

A digestive cartridge reduces intestinal injury in a murine model of necrotizing enterocolitis.

Sarah Z Wang, Djanira Fernandes, Savas T Tsikis, Thomas I Hirsch, Amy Pan, Mikayla Quigley, Valeria Ruiz, Scott C Fligor, Carter R Petty, Greta Loring and 3 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Sarah Z WangDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.
Djanira FernandesDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.
Savas T TsikisDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.
Thomas I HirschDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.
Amy PanDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.
Mikayla QuigleyDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.
Valeria RuizDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.ORCID https://orcid.org/0000-0002-4578-7017
Scott C FligorDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.
Carter R PettyBiostatistics and Research Design Center, Boston Children's Hospital, Boston, Massachusetts, United States of America.
Greta LoringAlcresta Therapeutics, Waltham, Boston, Massachusetts, United States of America.
Stephen DaviaAlcresta Therapeutics, Waltham, Boston, Massachusetts, United States of America.
Juhye KangDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.
Mark PuderDepartment of Surgery, Vascular Biology Program, Boston Children's Hospital, Boston, Massachusetts, United States of America.ORCID https://orcid.org/0000-0002-7941-2926

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFormula feeding is associated with necrotizing enterocolitis (NEC), a life-threatening gastrointestinal illness affecting premature infants. The presence of undigested fat in enteral formula may mediate NEC severity. The immobilized lipase cartridge (ILC) is an FDA-cleared digestive device that hydrolyzes triglyceride fat in formula into readily absorbable free fatty acids and monoglycerides. We hypothesized that use of a new ILC prototype designed to support increased feeding frequency in infants will reduce NEC mortality and disease severity in a murine model.

methodsNEC was induced in C57BL/6J mice from post-natal day 4-6 via oral gavage of lipopolysaccharide-containing formula 4x/day and hypoxia (5% O2) exposure 2x/day. Littermates were randomized to one of five groups: dam-fed (normal controls), ILC-digested formula, placebo-processed formula, NEC + ILC-digested formula, NEC+placebo-processed formula. Weights and mortality were measured daily. Mice were euthanized on P7 for assessment of NEC severity.

resultsNormal controls had better survival rates than formula-fed and NEC mice. The NEC + ILC group exhibited lower clinical and histologic severity scores compared to the NEC+placebo group on masked evaluation.

conclusionThe administration of formula pre-digested by the ILC improved clinical sickness, gut appearance, and histologic severity of NEC compared to placebo. These findings support further investigation of the ILC as a non-invasive, preventive therapy for NEC in humans.

Indexed as

Enterocolitis, NecrotizingIntestinesLipaseAnimalsAnimals, NewbornDisease Models, AnimalFemaleHumansMiceMice, Inbred C57BLLipase

Identifiers

PMID42060676
PMCPMC13132229

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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.