Evidence map›Paper›PMID 38542814›Full record

ArticleNutrients2024

Effects of NPY-2 Receptor Antagonists, Semaglutide, PYY

Simon Kloock, Niklas Haerting, Gloria Herzog, Marie Oertel, Niklas Geiger, Andreas Geier, Vasco Sequeira, Alexander Nickel, Michael Kohlhaas, Martin Fassnacht and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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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 2 institutions in 1 country.

Simon KloockDepartment of Internal Medicine, Division of Endocrinology and Diabetes, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.
Niklas HaertingDepartment of Internal Medicine, Division of Endocrinology and Diabetes, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.
Gloria HerzogInstitute of Pathology, University of Wuerzburg, 97070 Wuerzburg, Germany.
Marie OertelDepartment of Internal Medicine, Division of Endocrinology and Diabetes, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.
Niklas GeigerDepartment of Internal Medicine, Division of Endocrinology and Diabetes, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.ORCID 0009-0004-2163-8422
Andreas GeierDepartment of Internal Medicine, Division of Hepatology, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.
Vasco SequeiraComprehensive Heart Failure Center, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.ORCID 0000-0002-9192-7674
Alexander NickelComprehensive Heart Failure Center, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.
Michael KohlhaasComprehensive Heart Failure Center, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.
Martin FassnachtDepartment of Internal Medicine, Division of Endocrinology and Diabetes, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.ORCID 0000-0001-6170-6398
Ulrich DischingerDepartment of Internal Medicine, Division of Endocrinology and Diabetes, University Hospital Wuerzburg, University of Wuerzburg, 97080 Wuerzburg, Germany.
Universitätsklinikum Würzburg · DEUniversity of Würzburg · DE

Funding

IZKF Würzburg Z-3BC/01
6 · The paper itself

Abstract

(1) Background: Modulators of the Neuropeptide Y (NPY) system are involved in energy metabolism, but the effect of NPY receptor antagonists on metabolic-dysfunction-associated steatotic liver disease (MASLD), a common obesity-related comorbidity, are largely unknown. In this study, we report on the effects of antagonists of the NPY-2 receptor (Y2R) in comparison with empagliflozin and semaglutide, substances that are known to be beneficial in MASLD. (2) Methods: Diet-induced obese (DIO) male Wistar rats were randomized into the following treatment groups: empagliflozin, semaglutide ± PYY

Indexed as

BenzamidesBenzhydryl CompoundsFatty LiverGlucagon-Like PeptidesGlucosidesPiperazinesReceptors, Neuropeptide YAnimalsDietInflammationMaleObesityRatsRats, WistarSemaglutideWeight LossBenzamidesBenzhydryl CompoundsempagliflozinGlucagon-Like PeptidesGlucosidesJNJ-31020028PiperazinesReceptors, Neuropeptide YSemaglutidediabetesDIO ratsMASHMASLDneuropeptide YobesityPYYsemaglutide

Identifiers

PMID38542814
PMCPMC10974407
OpenAlexW4393043612

What OpenQuestion holds

Texttitle and abstract
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 OpenQuestion graph.