Evidence map›Paper›PMID 40949120›Full record

ArticleFrontiers in pharmacology2025

Opposing profiles of Netrin-1 and adiponectin in metabolic inflammation and insulin resistance.

María Guadalupe Ramos-Zavala, Jesús Jonathan García-Galindo, Alberto Beltrán-Ramírez, Luis Ricardo Balleza-Alejandri, Emiliano Peña-Durán, Alfredo Huerta-Huerta, Edy David Rubio-Arellano, Luis Daniel López-Murillo, Sara Pascoe-Gonzalez, Tannia Isabel Campos-Bayardo and 1 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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.

María Guadalupe Ramos-ZavalaDepartamento de Fisiología, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Mexico.
Jesús Jonathan García-GalindoDepartamento de Fisiología, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Mexico.
Alberto Beltrán-RamírezDepartamento de Fisiología, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Mexico.
Luis Ricardo Balleza-AlejandriHospital Médica de la Ciudad, Guadalajara, Mexico.
Emiliano Peña-DuránLicenciatura en Médico Cirujano y Partero, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Mexico.
Alfredo Huerta-HuertaHospital Médica de la Ciudad, Guadalajara, Mexico.
Edy David Rubio-ArellanoDepartamento de Fisiología, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Mexico.
Luis Daniel López-MurilloDepartamento de Fisiología, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Mexico.
Sara Pascoe-GonzalezInstitute of Experimental and Clinical Therapeutics (INTEC), Health Science University Center, Universidad de Guadalajara, Guadalajara, Mexico.
Tannia Isabel Campos-BayardoDepartamento de Fisiología, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Mexico.
Daniel Osmar Suárez-RicoDepartamento de Fisiología, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Obesity-driven low-grade inflammation contributes to insulin resistance (IR) and metabolic dysfunction. Beyond its axon-guidance role, Netrin-1 promotes macrophage retention in inflamed adipose tissue, whereas adiponectin exerts anti-inflammatory, insulin-sensitizing effects. We aimed to compare serum Netrin-1, interleukin-6 (IL-6), high-sensitivity C-reactive protein (hs-CRP), and adiponectin across metabolic profiles and assess their associations with systemic inflammation. Methods: We conducted an analytical cross-sectional study in adults (n = 60): metabolically healthy controls (C, n = 20), preclinical obesity (PO; HOMA-IR < 2.5, n = 20), and clinical obesity with insulin resistance (CO; HOMA-IR>2.5, n = 20). Anthropometrics, fasting glucose/insulin, lipid profile, and serum biomarkers were obtained; group differences and correlations were analyzed (non-parametric tests where appropriate). Results: Between-group testing showed higher Netrin-1 in CO versus controls (Kruskal-Wallis p = 0.013; C < CO), with no significant difference versus PO. IL-6 was elevated in both PO and CO versus controls (Kruskal-Wallis p < 0.001). hs-CRP peaked in PO versus both C and CO (Kruskal-Wallis p < 0.001). Adiponectin was lower in CO and inversely correlated with hs-CRP (r = -0.22) and IL-6 (r = -0.53, p < 0.001). Discussion: Circulating Netrin-1 and adiponectin display opposing profiles aligned with pro- versus anti-inflammatory signaling in metabolic dysfunction. These findings support the Netrin-1/adiponectin axis as an immunometabolic marker set in early IR states. The cross-sectional design limits causal inference; longitudinal studies integrating tissue-level measurements are warranted.

Indexed as

adiponectinHs-CRPIL-6inflammationinsulin resistancemacrophagesnetrin-1obesity

Identifiers

PMID40949120
PMCPMC12423091

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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.