Evidence map›Paper›PMID 41408640›Full record

ArticleJournal of translational medicine2025

Preliminary evaluation of oxyntomodulin as a biomarker for metabolic risk stratification in adults with obesity.

Mateusz Zwierz, Angelika Buczyńska, Maria Kościuszko, Katarzyna Sobieska, Agnieszka Adamska, Katarzyna Siewko, Adam Jacek Krętowski, Anna Popławska-Kita

Abstract read
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

8 authors.

Mateusz ZwierzDepartment of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Bialystok, 15-276, Poland. zwierzmateusz@wp.pl.ORCID 0009-0006-3806-9849
Angelika BuczyńskaClinical Research Centre, Medical University of Bialystok, Bialystok, 15-276, Poland.
Maria KościuszkoDepartment of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Bialystok, 15-276, Poland.
Katarzyna SobieskaDepartment of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Bialystok, 15-276, Poland.
Agnieszka AdamskaDepartment of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Bialystok, 15-276, Poland.
Katarzyna SiewkoDepartment of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Bialystok, 15-276, Poland.
Adam Jacek Krętowski *Department of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Bialystok, 15-276, Poland.
Anna Popławska-Kita *Department of Endocrinology, Diabetology and Internal Medicine, Medical University of Bialystok, Bialystok, 15-276, Poland.

Funding

Uniwersytet Medyczny w Bialymstoku Uniwersytet Medyczny w Bialymstoku
6 · The paper itself

Abstract

backgroundOxyntomodulin (OXM), secreted by enteroendocrine L-cells, regulates energy and glucose homeostasis and is a dual agonist of glucagon-like peptide-1 (GLP-1) and glucagon receptors (GCGRs), with anorexigenic, insulinotropic, and energy expenditure-enhancing effects. While synthetic analogues of OXM are under investigation as potential anti-obesity therapies, the physiological role and clinical significance of endogenous OXM in human obesity remain incompletely elucidated. This study aimed to evaluate fasting OXM levels and assess their association with anthropometric and biochemical parameters in individuals with varying degrees of excess weight.

methodsThe cross-sectional study included overweight (O1, n = 88) and obese (O2, n = 134) individuals, as well as a healthy control group (CG, n = 39). Body composition was assessed using dual-energy X-ray absorptiometry (DXA) and bioelectrical impedance analysis (BIA). Biochemical and hormonal analyses encompassed glucose-insulin homeostasis and lipid profile, with a focus on fasting OXM concentration. Insulin resistance (IR) and β-cell function were evaluated using validated indices.

resultsFasting OXM levels were significantly elevated in the O2 compared to both the O1 and CG (p < 0.0001). OXM positively correlated with several anthropometric parameters, including visceral adipose tissue (VAT) mass and volume in O2. Logistic regression showed that higher OXM was significantly associated with the risk of obesity. Additionally, an increase in the risk of IR and related metabolic complications was observed with an increase in OXM levels, mainly in advanced stages of weight gain.

conclusionsThese findings provide preliminary evidence that OXM constitutes a potential biomarker of visceral adiposity and early metabolic dysregulation, serving as a measurable indicator of IR in obesity.

Indexed as

BiomarkersObesityOxyntomodulinAdultBody CompositionCase-Control StudiesCross-Sectional StudiesFemaleHumansInsulin ResistanceMaleMiddle AgedRisk AssessmentRisk FactorsBiomarkersOxyntomodulinIncretin hormonesInsulin resistanceMetabolic biomarkersObesityOxyntomodulinVisceral adipose tissue

Identifiers

PMID41408640
PMCPMC12709701

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.