Evidence map›Paper›PMID 38327680›Full record

ArticleFrontiers in cellular and infection microbiology2023

Clinical characterization of a hypersensitivity mixed bacterial and fungal dermatitis in a translational model of porcine NASH.

Philipp Felgendreff, Josephine M Lawrence, Seyed M Hosseiniasl, Julie F Jacobs, Bruce P Amiot, Lisa Felgendreff, Anna Minshew, Ahmer Sultan, Boyukkhanim Ahmadzada, Michael C Rahe and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2023. 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, top 99% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

11 authors at 4 institutions in 2 countries.

Philipp Felgendreff *Department of Surgery, Mayo Clinic, Rochester, MN, United States.
Josephine M Lawrence *Department of Comparative Medicine, Mayo Clinic, Rochester, MN, United States.
Seyed M HosseiniaslDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Julie F JacobsDepartment of Comparative Medicine, Mayo Clinic, Rochester, MN, United States.
Bruce P AmiotDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Lisa FelgendreffCenter for Empirical Research in Economics and Behavioral Sciences, Media and Communication Science, University of Erfurt, Erfurt, Germany.
Anna MinshewDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Ahmer SultanDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Boyukkhanim AhmadzadaDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Michael C RaheVeterinary Diagnostic and Production Animal Medicine, Iowa State University, Ames, IA, United States.
Scott L NybergDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Mayo Clinic in Arizona · USIowa State University · USMedizinische Hochschule Hannover · DEUniversity of Erfurt · DE

Funding

Immunodeficient FAH-/- PigsR01DK106667 · NIDDK · MAYO CLINIC ROCHESTER · PI NYBERG, SCOTT L · 2015 to 2019
$2.1M
NIDDK NIH HHS R01 DK106667
6 · The paper itself

Abstract

Introduction: The development of animal models of chronic liver disease via diet modification is a promising avenue for translational research but can lead to unexpected side effects that impact model adoption. While these side effects are well characterized in rodent models of nonalcoholic steatohepatitis (NASH), limited knowledge of these effects exists for novel porcine models of NASH. To close this gap, the present study investigates the side effects of diet-based NASH induction in pigs, with a systematic analysis of the pathologic mechanisms underlying dermatitis development and evaluation of treatment approaches. Method: Twelve pigs (10 large domestic pigs, 2 Goettingen minipigs) were fed a methionine- and choline-deficient, high-fat diet for 8 weeks to induce NASH. A retrospective review of each animal's clinical record was performed to identify the side effects of the diet. Following the identification of diet-associated dermatitis, severity was judged by using a novel gradation system that characterized the individual lesions and body regions resulting in a cumulative evaluation. In addition to this clinical assessment, the etiology of the dermatitis was investigated via histopathologic and microbiologic testing. Furthermore, the success of prophylactic and therapeutic treatment approaches was evaluated by considering dermatitis development and clinical course. Results: All study animals demonstrated unexpected side effects of the methionine- and choline-deficient, high fat diet. In addition to marked dermatitis, study pigs showed impaired weight gain and developed steatorrhea and anemia. Based on the skin gradation system, five animals developed severe dermatitis, four animals moderate dermatitis, and three animals mild diet-associated dermatitis. Histological and microbiological evaluation of the affected skin showed signs of a hypersensitivity reaction with secondary infection by bacteria and fungi. The analysis showed that preemptive bathing extended the lesion-free duration by nearly 20 days. Furthermore, bathing in combination with a targeted antibiotic treatment represented a helpful treatment approach for diet-associated dermatitis. Conclusion: The provision of a methionine- and choline-deficient, high fat diet represents an effective approach for inducing NASH liver disease in pigs but predisposes study animals to multiple side effects. These side effects are universal to animals on study but can be adequately managed and do not represent a significant limitation of this model.

Indexed as

DermatitisNon-alcoholic Fatty Liver DiseaseAnimalsBacteriaCholineDietDiet, High-FatDisease Models, AnimalLiverMethionineMiceMice, Inbred C57BLRacemethionineRodentiaSwineSwine, MiniatureCholineMethionineRacemethioninedermatitislarge animal modelmicrobiomeNASHskin evaluation system

Identifiers

PMID38327680
PMCPMC10847572
OpenAlexW4391172311

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.