Evidence map›Paper›PMID 32000405›Full record

ArticleMedicine2020

Adiponectin receptor 1 gene is potentially associated with severity of postoperative pain but not cancer pain.

Jun Ninagawa, Masahiko Sumitani, Daisuke Nishizawa, Makoto Nagashima, Kazuhito Mietani, Hiroaki Abe, Reo Inoue, Jun Hozumi, Rikuhei Tsuchida, Kazutaka Ikeda and 1 more

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Interleukin-22 receptor 1-mediated stimulation of T-type CaCell communication and signaling : CCS · 2024
    Article
  3. 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

11 authors at 4 institutions in 2 countries.

Jun NinagawaDepartment of Anesthesiology and Pain Relief Center, The University of Tokyo Hospital.
Masahiko SumitaniDepartment of Pain and Palliative Medicine, The University of Tokyo Hospital.
Daisuke NishizawaAddictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo.
Makoto NagashimaDepartment of Surgery, Toho University Medical Center, Sakura Hospital, Chiba, Japan.
Kazuhito MietaniDepartment of Anesthesiology and Pain Relief Center, The University of Tokyo Hospital.
Hiroaki AbeDepartment of Pain and Palliative Medicine, The University of Tokyo Hospital.
Reo InoueDepartment of Anesthesiology and Pain Relief Center, The University of Tokyo Hospital.
Jun HozumiDepartment of Pain and Palliative Medicine, The University of Tokyo Hospital.
Rikuhei TsuchidaDepartment of Anesthesiology and Pain Relief Center, The University of Tokyo Hospital.
Kazutaka IkedaAddictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo.
Yoshitsugu YamadaDepartment of Anesthesiology and Pain Relief Center, The University of Tokyo Hospital.
Pain and Headache Center · USUniversity of Tokyo Hospital · JPNational Center For Child Health and Development · JPToho University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adiponectin is an adipose tissue-derived cytokine that exerts its antiinflammatory effects by binding to 2 adiponectin receptors, adiponectin receptor 1 (ADIPOR1) and adiponectin receptor 2 (ADIPOR2). However, the role of these adiponectin receptors on inflammatory pain remains unclear. We investigated the association between single nucleotide polymorphisms (SNPs) of these genes and inflammatory pain, such as postoperative pain and cancer pain.We analyzed 17 SNPs of the ADIPOR1 gene and 27 SNPs of the ADIPOR2 gene in 56 adult patients with postlaparotomy pain. We compared these genotypes with pain intensity and opioid consumption, adjusting for multiple testing. We analyzed the genotypes of 88 patients with cancer pain and examined the association of the relevant SNP(s) with pain intensity and opioid consumption.One variant of the ADIPOR1 gene (rs12045862) showed significant association with postoperative pain intensity; patients with minor allele homozygote (n = 7) demonstrated significantly worse pain intensity than that of combined patient group exhibiting major allele homozygote or the heterozygote (n = 49; Mann-Whitney test, P < .00002), although their opioid consumptions were comparable. Cancer pain intensity between minor allele homozygote patients (n = 7) and other 2 genotype patients (n = 81) were comparable.The rs12045862 SNP of the ADIPOR1 gene was associated with postoperative pain but not cancer pain. This might result from functional alteration of the ADIPOR1 signalling pathways, which influence the inflammatory process. ADIPOR1 may be a novel potential target for developing analgesics of postoperative pain.

Indexed as

Polymorphism, Single NucleotideAnalgesics, OpioidCancer PainColorectal NeoplasmsFemaleGenetic Association StudiesHumansInflammationLaparotomyMaleMiddle AgedPain MeasurementPostoperative PainReceptors, AdiponectinADIPOR1 protein, humanADIPOR2 protein, humanAnalgesics, OpioidReceptors, Adiponectin

Identifiers

PMID32000405
PMCPMC7004707
OpenAlexW3003631547

What OpenQuestion holds

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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.