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Results of upper cervical palpation test in migraine patients are not explained by pain sensitization

Our take

In migraine patients, does the upper cervical palpation test (UPT) measure pain sensitization or neck-related disability?

UPT subgroups in migraine patients were not explained by central sensitization, allodynia, pressure or mechanical pain thresholds, or neck disability scores. The test likely measures an independent construct, probably upper cervical musculoskeletal dysfunction at C1 and C2.

DescriptiveRead paper
Primary study42 ParticipantsLimited evidence

Key points

  1. UPT subgroups (no pain, local pain, referred pain) showed no statistically significant differences in central sensitization (CSI), allodynia (ASC-12), or pain threshold measures (all p > 0.05)
  2. 83% of migraine patients perceived local or referred neck pain during the UPT, consistent with prior studies
  3. Neck disability (NDI) was explained 43.6% by CSI and neck pain intensity, suggesting NDI in migraine populations reflects sensitization more than musculoskeletal dysfunction
  4. CSI was explained 49.4% by allodynia (ASC-12) and NDI, and the UPT did not significantly contribute (p = 0.056)
  5. The CSI may overestimate central sensitization in migraine patients because roughly one-third of its items describe typical migraine symptoms such as headache, nausea, and light sensitivity

How it was conducted

Design
Cross-sectional observational study with exploratory regression analysis; pre-registered on OSF
Participants
42 adults with episodic migraine (ICHD-3 criteria), at least 2 headache days per month, assessed pain-free and medication-free on the day of testing
UPT subgroups
No pain (n = 7), local pain (n = 17), referred pain (n = 18) based on sustained palpation at C1 and C2 transverse processes
Outcome measures
NDI (neck disability), CSI (central sensitization), ASC-12 (allodynia), mechanical pain threshold (MPT) and pressure pain threshold (PPT) at neck, trigeminal V1, and arm
Statistical approach
Kruskal-Wallis and chi-square for group differences; multinomial logistic regression for UPT subgroup prediction; multilinear regression for NDI and CSI as dependent variables

What they found

  • No significant differences across UPT subgroups for CSI (p = 0.167), NDI (p = 0.456), or ASC-12 (p = 0.759)
  • No significant differences across UPT subgroups for any MPT or PPT site (all p > 0.05, range p = 0.396 to 0.984)
  • Multinomial logistic regression model predicting UPT group was not significant (X2 = 10.540, df = 8, p = 0.229)
  • NDI was explained 43.6% by CSI (p < 0.001) and neck pain intensity (p = 0.032): model F = 16.870, p < 0.001, R2 adjusted = 0.436
  • CSI was explained 49.4% by ASC-12 (p = 0.006) and NDI (p < 0.001): model F = 14.328, p < 0.001, R2 adjusted = 0.494
  • 83% of patients perceived local or referred pain on UPT; 43% perceived referred pain to the head

Limitations

  • Very small subgroup sizes (no pain n = 7), limiting statistical power to detect real differences
  • Migraine cycle phase was not controlled - sensitization measures may differ between ictal, interictal, and postictal states
  • Only C1 and C2 were palpated; mid and lower cervical segments were not assessed, so the source of reported neck disability remains unclear
  • No imaging was performed to confirm upper cervical pathology identified by the UPT

Why it matters

For patients
Patients with migraine who experience neck pain during a cervical examination may have a mechanical upper cervical issue rather than simply heightened pain sensitivity, which could mean targeted physiotherapy is appropriate.
For clinicians
The NDI and CSI have limited utility for explaining UPT subgroup findings in migraine; clinicians should not assume a positive UPT is driven by central sensitization alone, and further investigation of C1-C2 musculoskeletal dysfunction is warranted.
For readers
This study challenges two common explanations for neck pain sensitivity in migraine and suggests the UPT captures a distinct, likely structural, cervical construct that needs validation in larger studies.

Source

doi:10.1038/s41598-025-03344-6

Read the original paper
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