Evidence map›Paper›PMID 32379222›Full record

ArticlePain2020

Brain gray matter abnormalities in osteoarthritis pain: a cross-sectional evaluation.

Joana Barroso, Andrew D Vigotsky, Paulo Branco, Ana Mafalda Reis, Thomas J Schnitzer, Vasco Galhardo, A Vania Apkarian

Open access · greenAbstract read
In one paragraph

Article in Pain, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it, 52 citations in OpenAlex.

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  18. Association ofNeurology · 2023
    Article
  19. Article
  20. Pain in Huntington's disease and its potential mechanisms.Frontiers in aging neuroscience · 2023
    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

7 authors at 2 institutions in 2 countries.

Joana BarrosoDepartamento de Biomedicina, Faculdade de Medicina, Instituto de Investigação e Inovação em Saúde-i3S, Universidade do Porto, Porto, Portugal.
Andrew D VigotskyDepartments of Biomedical Engineering and Statistics, Northwestern University, Evanston, IL, United States.
Paulo BrancoPhysiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
Ana Mafalda ReisUnilabs Boavista, Porto, Portugal.
Thomas J SchnitzerDepartments of Physical Medicine and Rehabilitation and.
Vasco GalhardoDepartamento de Biomedicina, Faculdade de Medicina, Instituto de Investigação e Inovação em Saúde-i3S, Universidade do Porto, Porto, Portugal.
A Vania ApkarianDepartments of Physical Medicine and Rehabilitation and.
Northwestern University · USi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PT

Funding

Rodent Behavior CoreP50DA044121 · NIDA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI APKARIAN, APKAR VANIA · 2018 to 2022
$9.0M
Brain Pathophysiology of Osteoarthritis PainR01AR074274 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI APKARIAN, APKAR VANIA · 2019 to 2023
$3.6M
NIAMS NIH HHS R01 AR074274NIDA NIH HHS P50 DA044121
6 · The paper itself

Abstract

abstractThe interaction between osteoarthritis (OA) pain and brain properties remains minimally understood, although anatomical and functional neuroimaging studies suggest that OA, similar to other chronic pain conditions, may impact as well as partly be determined by brain properties. Here, we studied brain gray matter (GM) properties in OA patients scheduled to undergo total joint replacement surgery. We tested the hypothesis that brain regional GM volume is distinct between hip OA (HOA) and knee OA (KOA) patients, relative to healthy controls and moreover, that these properties are related to OA pain. Voxel-based morphometry group contrasts showed lower anterior cingulate GM volume only in HOA. When we reoriented the brains (flipped) to examine the hemisphere contralateral to OA pain, precentral GM volume was lower in KOA and HOA, and 5 additional brain regions showed distortions between groups. These GM changes, however, did not reflect clinical parameters. Next, we subdivided the brain into larger regions, approximating Brodmann areas, and performed univariable and machine learning-based multivariable contrasts. The univariable analyses approximated voxel-based morphometry results. Our multivariable model distinguished between KOA and controls, was validated in a KOA hold-out sample, and generalized to HOA. The multivariable model in KOA, but not HOA, was related to neuropathic OA pain. These results were mapped into term space (using Neurosynth), providing a meta-analytic summary of brain anatomical distortions in OA. Our results indicate more subtle cortical anatomical differences in OA than previously reported and also emphasize the interaction between OA pain, namely its neuropathic component, and OA brain anatomy.

Indexed as

Chronic PainGray MatterBrainCross-Sectional StudiesHumansMagnetic Resonance Imaging

Identifiers

PMID32379222
PMCPMC7745790
OpenAlexW3021899581

What OpenQuestion holds

Textmetadata
LicenceTDM
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.