Evidence map›Paper›PMID 31567972›Full record

ArticleMedicine2019

Serum cytokine, chemokine, and growth factor profiles and their modulation in inflammatory bowel disease.

Margarita L Martinez-Fierro, Idalia Garza-Veloz, Maria R Rocha-Pizaña, Edith Cardenas-Vargas, Miguel A Cid-Baez, Fabiola Trejo-Vazquez, Virginia Flores-Morales, Gabriela A Villela-Ramirez, Ivan Delgado-Enciso, Iram P Rodriguez-Sanchez and 1 more

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

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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 4 institutions in 1 country.

Margarita L Martinez-FierroMolecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS.
Idalia Garza-VelozMolecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS.
Maria R Rocha-PizañaTecnologico de Monterrey, Escuela de Ingenieria y Ciencias, Puebla.
Edith Cardenas-VargasMolecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS.
Miguel A Cid-BaezMolecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS.
Fabiola Trejo-VazquezMolecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS.
Virginia Flores-MoralesLaboratorio de Sintesis Asimetrica y Bioenergetica (LSAyB), Ingenieria Quimica, Universidad Autonoma de Zacatecas, Zacatecas.
Gabriela A Villela-RamirezMolecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS.
Ivan Delgado-EncisoSchool of Medicine, University of Colima, and Cancerology State Institute, Colima State Health Services, Colima.
Iram P Rodriguez-SanchezLaboratorio de Fisiologia Molecular y Estructural, Facultad de Ciencias Biologicas, Universidad Autonoma de Nuevo Leon, Monterrey Nuevo Leon, Mexico.
Yolanda Ortiz-CastroMolecular Medicine Laboratory, Unidad Academica de Medicina Humana y CS.
Universidad Autónoma de Zacatecas "Francisco García Salinas" · MXInstitute for Social Security and Services for State Workers · MXTecnológico de Monterrey · MXUniversidad de Colima · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ulcerative colitis (UC) and Crohn disease (CD) are the most common forms of inflammatory bowel disease (IBD). Because these subtypes of IBD are characterized by periods of activity and remission, an understanding of the modulation of biochemical markers with the clinical features of IBD or its treatment, may be useful for determining the correct treatment protocol.This study aimed to evaluate the serum levels of 27 protein biomarkers to determine their association with IBD, correlation with clinical findings of disease, and modulation according to the pharmacologic therapy.A case-control study was carried out in Zacatecas, Mexico. The 27 protein profiles of serum from 53 participants (23 UC, 11 CD, and 19 controls) were evaluated using the Pro Human Cytokine 27-Plex immunoassay (Bio-Rad).Considering the controls as a reference, the group with IBD endoscopic activity showed higher serum levels of granulocyte colony-stimulating factor (G-CSF), interleukin 1 receptor antagonist (IL-1Ra), and platelet-derived growth factor BB (PDGF-BB) (P < .05). Interferon-induced protein 10 (IP-10) was associated with extraintestinal symptoms of disease (P = .041). Both PDGF-BB and interleukin 6 (IL-6) showed the strongest correlations with clinical features of IBD. Levels of IL-6, IL-7, and monocyte chemoattractant protein 1 were higher with 5-aminosalicylic acid (5-ASA) + Azathioprine therapy than controls (P < .05). Combined therapy with 5-ASA + Adalimumab led to the strongest changes in marker modulation: IL-4, IL-5, IL-15, and PDGF-BB, were upregulated (P < .05).Elevated serum levels of G-CSF, IL-1Ra, and PDGF-BB were associated with IBD endoscopic activity, and of IP-10 with extraintestinal manifestations of IBD. Combined therapy of 5-ASA + Adalimumab produced significant upregulation of IL-4, IL-5, IL-15, and PDGF-BB. This information may be useful for deciding on the course of pharmacologic therapy for patients with IBD and for generating new therapy alternatives to improve the outcome of patients with IBD.

Indexed as

AdalimumabAdultAgedAnti-Inflammatory AgentsAzathioprineBecaplerminBiomarkersCase-Control StudiesChemokine CXCL10ChemokinesCytokinesFemaleGranulocyte Colony-Stimulating FactorHumansInflammatory Bowel DiseasesIntercellular Signaling Peptides and ProteinsAdalimumabAnti-Inflammatory AgentsAzathioprineBecaplerminBiomarkersChemokine CXCL10ChemokinesCXCL10 protein, humanCytokinesGranulocyte Colony-Stimulating FactorIntercellular Signaling Peptides and ProteinsInterleukin-6MesalamineReceptors, Interleukin-1

Identifiers

PMID31567972
PMCPMC6756690
OpenAlexW2978901884

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.