Evidence map›Paper›PMID 40035629›Full record

ArticlePain2025

Evidence for peripheral neuroinflammation after acute whiplash.

Colette Ridehalgh, Joel Fundaun, Stephen Bremner, Mara Cercignani, Soraya Koushesh, Rupert Young, Alex Novak, Jane Greening, Annina B Schmid, Andrew Dilley

Abstract read
In one paragraph

Article in Pain, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

10 authors.

Colette RidehalghDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Trafford Centre, University of Sussex, Falmer, Brighton, United Kingdom.
Joel FundaunNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
Stephen BremnerDepartment of Primary Care and Public Health, Brighton and Sussex Medical School, Brighton, United Kingdom.
Mara CercignaniCardiff University Brain Research Imaging Centre, Cardiff University, Cardiff, United Kingdom.
Soraya KousheshNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
Rupert YoungSchool of Engineering and Informatics, University of Sussex, Brighton, United Kingdom.
Alex NovakEmergency Medicine Research Oxford (EMROx), Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
Jane GreeningDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Trafford Centre, University of Sussex, Falmer, Brighton, United Kingdom.
Annina B SchmidNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
Andrew DilleyDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Trafford Centre, University of Sussex, Falmer, Brighton, United Kingdom.

Funding

Versus Arthritis 22465Wellcome Trust
6 · The paper itself

Abstract

abstractWhiplash injury is associated with high socioeconomic costs and poor prognosis. Most people are classified as having whiplash-associated disorder grade II (WADII), with neck complaints and musculoskeletal signs, in the absence of frank neurological signs. However, evidence suggests that there is a subgroup with underlying nerve involvement in WADII, such as peripheral neuroinflammation. This study aimed to investigate the presence of neuroinflammation in acute WADII using T2-weighted magnetic resonance imaging of the brachial plexus, dorsal root ganglia and median nerve, and clinical surrogates of neuroinflammation: heightened nerve mechanosensitivity (HNM), raised serum inflammatory mediators, and somatosensory hyperalgesia. One hundred twenty-two WADII participants within 4 weeks of whiplash and 43 healthy controls (HCs) were recruited. Magnetic resonance imaging T2 signal ratio was increased in the C5 root of the brachial plexus and the C5-C8 dorsal root ganglia in WADII participants compared with HCs but not in the distal median nerve trunk. Fifty-five percent of WADII participants had signs of HNM. Inflammatory mediators were also raised compared with HCs, and 47% of WADII participants had somatosensory changes on quantitative sensory testing. In those WADII individuals with HNM, there was hyperalgesia to cold and pressure and an increased proportion of neuropathic pain. Many people with WADII had multiple indicators of neuroinflammation. Overall, our results present a complex phenotypic profile for acute WADII and provide evidence suggestive of peripheral neuroinflammation in a subgroup of individuals. The results suggest that there is a need to reconsider the management of people with WADII.

Indexed as

Neuroinflammatory DiseasesWhiplash InjuriesAdultBrachial PlexusFemaleGanglia, SpinalHumansHyperalgesiaMagnetic Resonance ImagingMaleMedian NerveMiddle AgedYoung AdultHeightened nerve mechanosensitivityMagnetic resonance imagingNeuritisNeuroinflammationNeuropathic painQuantitative sensory testingWhiplashWhiplash associated disorder

Identifiers

PMID40035629
PMCPMC12444895

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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.