Evidence map›Paper›PMID 40501484›Full record

ArticleNeurobiology of pain (Cambridge, Mass.)

Patient phenotyping for molecular profiling of neck and low back pain - Study protocol.

Michele Curatolo, Cathryn Payne, Abby P Chiu, Nguyen T Tran, Natalie Yap, Christoph P Hofstetter, Joseph B Lesnak, Asta Arendt-Tranholm, Theodore J Price, Jeffrey G Jarvik and 1 more

Abstract read
In one paragraph

Article in Neurobiology of pain (Cambridge, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Michele CuratoloDepartment of Anesthesiology and Pain Medicine, University of Washington, Seattle WA, USA.
Cathryn PayneDepartment of Neurological Surgery, University of Washington, Seattle WA, USA.
Abby P ChiuDepartment of Anesthesiology and Pain Medicine, University of Washington, Seattle WA, USA.
Nguyen T TranDepartment of Neurological Surgery, University of Washington, Seattle WA, USA.
Natalie YapDepartment of Neurological Surgery, University of Washington, Seattle WA, USA.
Christoph P HofstetterDepartment of Neurological Surgery, University of Washington, Seattle WA, USA.
Joseph B LesnakCenter for Advanced Pain Studies, Department of Neuroscience, University of Texas at Dallas, Richardson, TX, USA.
Asta Arendt-TranholmCenter for Advanced Pain Studies, Department of Neuroscience, University of Texas at Dallas, Richardson, TX, USA.
Theodore J PriceCenter for Advanced Pain Studies, Department of Neuroscience, University of Texas at Dallas, Richardson, TX, USA.
Jeffrey G JarvikDepartment of Radiology, University of Washington, Seattle WA, USA.
Judith A TurnerDepartment of Psychiatry & Behavioral Sciences, University of Washington, Seattle WA, USA.

Funding

UW Core Center for Clinical Research of Musculoskeletal ConditionsP30AR072572 · NIAMS · UNIVERSITY OF WASHINGTON · PI JEFFREY G JARVIK, Pradeep Suri · 2017 to 2026
$8.3M
Identifying novel therapeutic targets for chronic neck pain: RNA-sequencing in human painful atlanto-axial arthropathyR01AR078192 · NIAMS · UNIVERSITY OF WASHINGTON · PI Michele Curatolo, Christoph Paul Hofstetter · 2021 to 2026
$3.6M
NIAMS NIH HHS P30 AR072572NIAMS NIH HHS R01 AR078192
6 · The paper itself

Abstract

Background: Chronic neck and low back pain are highly prevalent, leading causes of disability, and associated with long-term opioid use. The development of effective therapeutics is hampered by the limited understanding of the molecular mechanisms underlying these conditions. The Human Nociceptor and Spinal Cord Molecular Signature Center is a consortium within the NIH PRECISION Human Pain Network. The Center aims to fundamentally advance the understanding of the molecular neurobiology and neuroimmunology underlying human neck and low back pain, thereby enabling the discovery of therapeutic targets. We are pursuing this aim by applying bulk, single cell and spatial transcriptomics to tissues recovered from patients with neck and low back pain undergoing C1-2 and lumbar arthrodesis. The C2 dorsal root ganglion, facet joints, muscles, fascia, and intervertebral discs are harvested; control tissues are obtained from organ donors. A critical advantage of human research is the study of molecular neurobiological mechanisms in the context of the phenotypic complexity of chronic pain. The aim of this article is to summarize the rationale and methods used in our project to phenotype patients. Methods: Phenotyping domains include pain-related characteristics such as pain intensity, duration, and location; physical function; psychosocial function; neuropathic components assessed by self-report and quantitative sensory testing; somatosensory functions such as mechanical pain sensitivity and temporal summation; and radiological findings. Conclusion: We anticipate that comprehensive phenotyping will greatly facilitate the identification of phenotype-specific transcriptional signatures associated with chronic neck and low back pain, revealing new neurobiological and/or neuro-immunological mechanisms of painful diseases.

Indexed as

Low back painNeck painPhenotypingRNA-sequencing

Identifiers

PMID40501484
PMCPMC12152350

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.