Evidence map›Paper›PMID 25592233›Full record

Trial reportJournal of translational medicine2015

The number of circulating monocytes as biomarkers of the clinical response to methotrexate in untreated patients with rheumatoid arthritis.

Luis Chara, Ana Sánchez-Atrio, Ana Pérez, Eduardo Cuende, Fernando Albarrán, Ana Turrión, Julio Chevarria, Angel Asunsolo del Barco, Miguel A Sánchez, Jorge Monserrat and 5 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Journal of translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.0field-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

33 citing papers in PubMed, 59 citations in OpenAlex.

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  17. Review
  18. Review
  19. Rheumatoid arthritis CD14Clinical & translational immunology · 2021
    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

15 authors at 3 institutions in 2 countries.

Luis CharaDepartment of Medicine, University of Alcalá, Carretera Madrid-Barcelona km 33.600, 28871, Alcalá de Henares, Madrid, Spain. lucho_chara@yahoo.com.
Ana Sánchez-AtrioImmune System Diseases-Rheumatology and Oncology Service, University Hospital "Príncipe de Asturias", Alcalá de Henares, Madrid, Spain. aisatrio@gmail.com.
Ana PérezImmune System Diseases-Rheumatology and Oncology Service, University Hospital "Príncipe de Asturias", Alcalá de Henares, Madrid, Spain. aperezalcala@yahoo.es.
Eduardo CuendeImmune System Diseases-Rheumatology and Oncology Service, University Hospital "Príncipe de Asturias", Alcalá de Henares, Madrid, Spain. ecuende@gmail.com.
Fernando AlbarránImmune System Diseases-Rheumatology and Oncology Service, University Hospital "Príncipe de Asturias", Alcalá de Henares, Madrid, Spain. fernando.albarran@uah.es.
Ana TurriónImmune System Diseases-Rheumatology and Oncology Service, University Hospital "Príncipe de Asturias", Alcalá de Henares, Madrid, Spain. anaturrion@hotmail.com.
Julio ChevarriaImmune System Diseases-Rheumatology and Oncology Service, University Hospital "Príncipe de Asturias", Alcalá de Henares, Madrid, Spain. juliochevarria@yahoo.com.
Angel Asunsolo del BarcoDepartment of Health and Medical Social Sciences, University of Alcalá, Madrid, Spain. angel.asunsolo@uah.es.
Miguel A SánchezDepartment of Medicine, University of Alcalá, Carretera Madrid-Barcelona km 33.600, 28871, Alcalá de Henares, Madrid, Spain. smimasl@hotmail.com.
Jorge MonserratDepartment of Medicine, University of Alcalá, Carretera Madrid-Barcelona km 33.600, 28871, Alcalá de Henares, Madrid, Spain. jorge.monserrat@uah.es.
Alfredo PrietoDepartment of Medicine, University of Alcalá, Carretera Madrid-Barcelona km 33.600, 28871, Alcalá de Henares, Madrid, Spain. alfredo.prieto@uah.es.
Antonio de la HeraDepartment of Medicine, University of Alcalá, Carretera Madrid-Barcelona km 33.600, 28871, Alcalá de Henares, Madrid, Spain. antonio.delahera@uah.es.
Ignacio SanzDivision of Allergy, Immunology and Rheumatology, Department of Medicine, Emory University, Atlanta, GA, USA. ignacio.sanz@emory.edu.
David DiazDepartment of Medicine, University of Alcalá, Carretera Madrid-Barcelona km 33.600, 28871, Alcalá de Henares, Madrid, Spain. david.diaz@uah.es.
Melchor Alvarez-MonDepartment of Medicine, University of Alcalá, Carretera Madrid-Barcelona km 33.600, 28871, Alcalá de Henares, Madrid, Spain. mademons@gmail.com.
Hospital Universitario Príncipe de Asturias · ESUniversidad de Alcalá · ESEmory University · US

Funding

Regulation of B cell Responses in SLE and Other Autoimmune DiseasesU19AI110483 · NIAID · EMORY UNIVERSITY · PI JEREMY M. BOSS · 2014 to 2026
$76.6M
Translational Research Project Effector and Regulatory B cells in SLEU19AI056390 · NIAID · UNIVERSITY OF ROCHESTER · PI LOONEY, RICHARD JOHN · 2003 to 2013
$8.9M
A Model System for the Study of Human B-cell ToleranceR37AI049660 · NIAID · UNIVERSITY OF ROCHESTER · PI SANZ, IGNACIO E. · 2010 to 2019
$3.7M
NIAID NIH HHS R37 AI049660NIAID NIH HHS U19 AI056390NIAID NIH HHS U19 AI110483
6 · The paper itself

Abstract

backgroundThe aim of this work was to analyze the number and distribution of circulating monocytes, and of their CD14(+high)CD16(-), CD14(+high)CD16(+) and CD14(+low)CD16(+) subset cells, in treatment-naive patients with rheumatoid arthritis (RA), and to determine their value in predicting the clinical response to methotrexate (MTX) treatment.

methodsThis prospective work investigated the number of circulating monocytes, and the numbers of CD14(+high)CD16(-), CD14(+high)CD16(+) and CD14(+low)CD16(+) subset cells, in 52 untreated patients with RA before MTX treatment, and at 3 and 6 months into treatment, using flow cytometry.

resultsThe absolute number of circulating monocytes, and the numbers of CD14(+high)CD16(-), CD14(+high)CD16(+) and CD14(+low)CD16(+) subset cells, were significantly higher in MTX non-responders than in responders and healthy controls before starting and throughout treatment. Responders showed normal numbers of monocytes, and of their subset cells, over the study period. The pre-treatment absolute number of circulating monocytes, and the numbers of CD14(+high)CD16(-) and CD14(+high)CD16(+) subset cells, were found to be predictive of the clinical response to MTX, with a sensitivity and specificity of >70% and >88%, respectively.

conclusionsTreatment-naive patients with RA showed an anomalous distribution of circulating monocyte subsets, and an anomalous number of cells in each subset. A higher pre-treatment number of circulating monocytes, and higher numbers of CD14(+high)CD16(-) and CD14(+high)CD16(+) subset cells, predict a reduced clinical response to MTX in untreated patients with RA.

Indexed as

Cell MovementAntigens, CDArthritis, RheumatoidBiomarkersCase-Control StudiesCell CountCX3C Chemokine Receptor 1DemographyFemaleHumansMaleMethotrexateMiddle AgedMonocytesReceptors, ChemokineROC CurveAntigens, CDBiomarkersCX3C Chemokine Receptor 1CX3CR1 protein, humanMethotrexateReceptors, Chemokine

Identifiers

PMID25592233
PMCPMC4310181
OpenAlexW2130509386

What OpenQuestion holds

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LicenceCC BY
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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.