Evidence map›Paper›PMID 40789651›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2025

Cyclic infusion mitigates liver dysfunction associated with continuous total parenteral nutrition in a novel murine model.

Nathaniel B Willis, Tahliyah S Mims, Karen Antunes, Hubert Peng, Mei-I Yen, Chi-Liang Eric Yen, Joseph F Pierre

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

Nathaniel B WillisDepartment of Nutritional Sciences, College of Agriculture and Life Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States.ORCID 0000-0003-1401-8204
Tahliyah S MimsDepartment of Nutritional Sciences, College of Agriculture and Life Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States.
Karen AntunesDepartment of Nutritional Sciences, College of Agriculture and Life Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States.
Hubert PengDepartment of Nutritional Sciences, College of Agriculture and Life Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States.ORCID 0000-0003-4881-1331
Mei-I YenDepartment of Nutritional Sciences, College of Agriculture and Life Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States.
Chi-Liang Eric YenDepartment of Nutritional Sciences, College of Agriculture and Life Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States.ORCID 0000-0002-7408-7503
Joseph F PierreDepartment of Nutritional Sciences, College of Agriculture and Life Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States.ORCID 0000-0002-4248-1290

Funding

TRAINING IN NUTRITIONT32DK007665 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI GUY E GROBLEWSKI, Chi- Liang Eric Yen · 1993 to 2026
$9.2M
Determining the contribution of microbial-derived metabolites to protective immunity in obesity-driven cancer risk.U01CA272541 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI Liza Makowski-Hayes, Joseph F PIERRE · 2022 to 2026
$5.1M
Exploring the role, regulation, and antimicrobial function of Paneth cell peptides PYY and NPY in maintaining gut microbial commensalism and innate immune defenseR01DK113788 · NIDDK · UNIVERSITY OF CHICAGO · PI EUGENE B CHANG, Joseph F PIERRE · 2017 to 2026
$4.6M
Role of microbial-modulated bile acid receptor signaling in breast cancerR01CA253329 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI Katherine Loree Cook, Liza Makowski-Hayes · 2020 to 2026
$3.0M
Small Animal Metabolic Phenotyping FacilityS10OD028739 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI YEN, CHI- LIANG ERIC · 2020 to 2020
$685k
HHS | National Institutes of Health (NIH) CA253329HHS | National Institutes of Health (NIH) CA272541HHS | National Institutes of Health (NIH) DK007665HHS | National Institutes of Health (NIH) OD028739NCI NIH HHS R01 CA253329NCI NIH HHS U01 CA272541NIDDK NIH HHS R01 DK113788NIDDK NIH HHS T32 DK007665NIH HHS S10 OD028739
6 · The paper itself

Abstract

Parenteral nutrition (PN) is a lifesaving intervention for patients unable to feed enterally but is often associated with parenteral nutrition-associated liver disease (PNALD), also called intestinal failure-associated liver disease (IFALD). This disease is characterized by steatosis, cholestasis, and elevated liver stress markers. Continuous PN induces hepatic injury through mechanisms including insulin resistance, lipotoxicity, systemic inflammation, and oxidative stress. Infusion cycling is known to ameliorate clinical markers of liver injury, but metabolic underpinnings have not been thoroughly investigated. Therefore, we modeled PN-induced liver injury in mice to investigate how differential infusion patterns impacted hepatic metabolism. Intermittent infusions protected against increased circulating alanine aminotransferase levels and improved histopathology to more closely resemble chow controls. Transcriptomic analyses revealed 804 differentially expressed genes between PN groups, highlighting pathways related to peroxisome proliferator-activated receptor signaling, fatty acid metabolism, and peroxisomes. Relative to the continuous group, intermittent PN infusion specifically downregulated

Indexed as

LiverLiver DiseasesParenteral Nutrition, TotalAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLOxidative Stresslipid oxidationperoxisomePNALDrespiratory exchange rate

Identifiers

PMID40789651
PMCPMC12456138

What OpenQuestion holds

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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.