Evidence map›Paper›PMID 36361779›Full record

SynthesisInternational journal of molecular sciences2022

miRNA-Mediated Epigenetic Regulation of Treatment Response in RA Patients-A Systematic Review.

Arkaitz Mucientes, Jose Manuel Lisbona, Natalia Mena-Vázquez, Patricia Ruiz-Limón, Sara Manrique-Arija, Antonio Fernández-Nebro

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. 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

6 authors at 2 institutions in 1 country.

Arkaitz MucientesInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina-IBIMA Plataforma Bionand, 29010 Málaga, Spain.ORCID 0000-0002-7431-7225
Jose Manuel LisbonaInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina-IBIMA Plataforma Bionand, 29010 Málaga, Spain.ORCID 0000-0002-9125-2208
Natalia Mena-VázquezInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina-IBIMA Plataforma Bionand, 29010 Málaga, Spain.ORCID 0000-0001-6173-2051
Patricia Ruiz-LimónInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina-IBIMA Plataforma Bionand, 29010 Málaga, Spain.ORCID 0000-0003-3820-428X
Sara Manrique-ArijaInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina-IBIMA Plataforma Bionand, 29010 Málaga, Spain.ORCID 0000-0003-2284-7846
Antonio Fernández-NebroInstituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina-IBIMA Plataforma Bionand, 29010 Málaga, Spain.ORCID 0000-0002-2962-9844
Hospital Regional Universitario de Málaga · ESInstituto de Salud Carlos III · ES

Funding

Instituto de Salud Carlos III FIS Grant PI22/01207Instituto de Salud Carlos III RICORS RD21/0002/0037Instituto de Salud Carlos III Sara Borrel CD19-00216
6 · The paper itself

Abstract

This study aimed to evaluate the role of microRNAs (miRNA) as biomarkers of treatment response in rheumatoid arthritis (RA) patients through a systematic review of the literature. The MEDLINE and Embase databases were searched for studies including RA-diagnosed patients treated with disease-modifying antirheumatic drugs (DMARDs) that identify miRNAs as response predictors. Review inclusion criteria were met by 10 studies. The main outcome of the study was the response to treatment, defined according to EULAR criteria. A total of 839 RA patients and 67 healthy donors were included in the selected studies. RA patients presented seropositivity for the rheumatoid factor of 74.7% and anti-citrullinated C-peptide antibodies of 63.6%. After revision, 15 miRNAs were described as treatment response biomarkers for methotrexate, anti-tumour necrosis factor (TNF), and rituximab. Among treatments, methotrexate presented the highest number of predictor miRNAs: miR-16, miR-22, miR-132, miR-146a and miR-155. The most polyvalent miRNAs were miR-146a, predicting response to methotrexate and anti-TNF, and miR-125b, which predicts response to infliximab and rituximab. Our data support the role of miRNAs as biomarkers of treatment response in RA and point to DMARDs modifying the miRNAs expression. Nevertheless, further studies are needed since a meta-analysis that allows definitive conclusions is not possible due to the lack of studies in this field.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidMicroRNAsBiomarkersEpigenesis, GeneticHumansMethotrexateRituximabTreatment OutcomeTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAntirheumatic AgentsBiomarkersMethotrexateMicroRNAsRituximabTumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitorsbiomarkerdisease-modifying antirheumatic drugmicroRNArheumatoid arthritissystemic reviewtreatment

Identifiers

PMID36361779
PMCPMC9657910
OpenAlexW4307358087

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.