Evidence map›Paper›PMID 36768285›Full record

ArticleInternational journal of molecular sciences2023

Serum Levels of IFABP2 and Differences in

Oscar Zaragoza-García, Natividad Castro-Alarcón, Gloria Pérez-Rubio, Ramcés Falfán-Valencia, Olivia Briceño, José Eduardo Navarro-Zarza, Isela Parra-Rojas, Mario Tello, Iris Paola Guzmán-Guzmán

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

9 authors.

Oscar Zaragoza-GarcíaFaculty of Chemical-Biological Sciences, Autonomous University of Guerrero, Chilpancingo 39087, Mexico.ORCID 0000-0001-9006-2165
Natividad Castro-AlarcónFaculty of Chemical-Biological Sciences, Autonomous University of Guerrero, Chilpancingo 39087, Mexico.
Gloria Pérez-RubioHLA Laboratory, National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City 14080, Mexico.ORCID 0000-0002-6876-1012
Ramcés Falfán-ValenciaHLA Laboratory, National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City 14080, Mexico.ORCID 0000-0001-6877-8124
Olivia BriceñoInfectious Diseases Research Center, National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City 14080, Mexico.
José Eduardo Navarro-ZarzaDepartment of Medical Internal, General Hospital Raymundo Abarca Alarcón, Chilpancingo 39019, Mexico.
Isela Parra-RojasFaculty of Chemical-Biological Sciences, Autonomous University of Guerrero, Chilpancingo 39087, Mexico.
Mario TelloBacterial Metagenomics Laboratory, Faculty of Chemistry and Biology, University of Santiago of Chile, Santiago 8320000, Chile.ORCID 0000-0003-4573-6460
Iris Paola Guzmán-GuzmánFaculty of Chemical-Biological Sciences, Autonomous University of Guerrero, Chilpancingo 39087, Mexico.ORCID 0000-0003-1535-4226

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal dysbiosis is related to the physiopathology and clinical manifestation of rheumatoid arthritis (RA) and the response to pharmacologic treatment. The objectives of this study were (1) to analyze the effect of conventional synthetic disease modifying anti-rheumatic drugs (csDMARDs) on the abundance of gut microbiota's bacteria; (2) to evaluate the relationship between the differences in microbial abundance with the serum levels of intestinal fatty-acid binding protein 2 (IFABP2), cytokines, and the response phenotype to csDMARDs therapy in RA. A cross-sectional study was conducted on 23 women diagnosed with RA. The abundance of bacteria in gut microbiota was determined with qPCR. The ELISA technique determined serum levels of IFABP2, TNF-α, IL-10, and IL-17A. We found that the accumulated dose of methotrexate or prednisone is negatively associated with the abundance of

Indexed as

Antirheumatic AgentsArthritis, RheumatoidGastrointestinal MicrobiomeLactobacillusCell Membrane PermeabilityCross-Sectional StudiesFatty Acid-Binding ProteinsFemaleHumansInterleukin-17IntestinesPilot ProjectsPorphyromonas gingivalisTumor Necrosis Factor-alphaAntirheumatic AgentsFABP2 protein, humanFatty Acid-Binding ProteinsInterleukin-17Tumor Necrosis Factor-alphagut microbiotaintestinal fatty-acid binding protein 2intestinal permeabilitynon-responserheumatoid arthritistherapy

Identifiers

PMID36768285
PMCPMC9916456

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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 OpenQuestion graph.