Evidence map›Paper›PMID 36833338›Full record

SynthesisGenes2023

Transient Receptor Potential Ankyrin 1 (TRPA1) Methylation and Chronic Pain: A Systematic Review.

Fulvio Celsi, Francesca Peri, Julia Cavasin, Luisa Zupin, Giorgio Cozzi, Egidio Barbi, Sergio Crovella

Open access · goldAbstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. The role of TRPA1 in lung cancer.Translational lung cancer research · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Article
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

7 authors at 3 institutions in 2 countries.

Fulvio CelsiInstitute for Maternal and Child Health-IRCCS Burlo Garofolo, 34137 Trieste, Italy.ORCID 0000-0002-9760-8463
Francesca PeriDepartment of Medicine, Surgery, and Health Sciences, University of Trieste, 34127 Trieste, Italy.
Julia CavasinDepartment of Medicine, Surgery, and Health Sciences, University of Trieste, 34127 Trieste, Italy.
Luisa ZupinInstitute for Maternal and Child Health-IRCCS Burlo Garofolo, 34137 Trieste, Italy.ORCID 0000-0001-5886-9129
Giorgio CozziInstitute for Maternal and Child Health-IRCCS Burlo Garofolo, 34137 Trieste, Italy.ORCID 0000-0002-6427-1366
Egidio BarbiInstitute for Maternal and Child Health-IRCCS Burlo Garofolo, 34137 Trieste, Italy.
Sergio CrovellaBiological Science Program, Department of Biological and Environmental Sciences, College of Arts and Sciences, Qatar University, Doha 2713, Qatar.ORCID 0000-0001-8493-1168
IRCCS Materno Infantile Burlo Garofolo · ITUniversity of Trieste · ITQatar University · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveChronic pain represents a major global health issue in terms of psycho-physiological, therapeutic, and economic burden, not limited to adults but also to the pediatric age. Despite its great impact, its molecular mechanisms have still not been completely unraveled. Focusing on the impact of epigenetics in the pain complex trait, we assessed the association between chronic pain and the methylation pattern of TRPA1, a key gene related to pain sensitivity.

methodsWe conducted a systematic review retrieving articles from three different databases. After deduplication, 431 items were subjected to manual screening, and then 61 articles were selected and screened again. Of these, only six were maintained for meta-analysis and analyzed using specific R packages.

resultsSix articles were divided into two groups (group 1: comparison of mean methylation levels between healthy subjects and patients with chronic pain; group 2: correlation between mean methylation levels and pain sensation). A non-significant mean difference was obtained from the analysis of group 1 with a value of 3.97 (95% C.I. -7.79; 15.73). Analysis of group 2 showed a high level of variability between studies (correlation = 0.35, 95% C.I. -0.12; 0.82) due to their heterogeneity (I

conclusionsDespite the high variability observed in the different studies analyzed, our results suggest that hypermethylation and increased pain sensitivity could be connected, possibly due to the variation of TRPA1 expression.

Indexed as

Chronic PainTRPA1 Cation ChannelAdultAnkyrinsChildDNA MethylationEpigenesis, GeneticHumansAnkyrinsTRPA1 Cation ChannelTRPA1 protein, humanmethylationpainTRPA1

Identifiers

PMID36833338
PMCPMC9957263
OpenAlexW4319317000

What OpenQuestion 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 OpenQuestion graph.