Evidence map›Paper›PMID 36756979›Full record

ArticleCephalalgia : an international journal of headache2023

Longitudinal differences in iron deposition in periaqueductal gray matter and anterior cingulate cortex are associated with response to erenumab in migraine.

Simona Nikolova, Catherine Daniela Chong, Gina M Dumkrieger, Jing Li, Teresa Wu, Todd J Schwedt

Open access · hybridAbstract read
In one paragraph

Article in Cephalalgia : an international journal of headache, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Evidence of Involvement of the Calcitonin Gene-Related Peptide in Restless Legs Syndrome.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  6. Article
  7. Application of Artificial Intelligence in the Headache Field.Current pain and headache reports · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. 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

6 authors at 3 institutions in 1 country.

Simona NikolovaDepartment of Neurology, Mayo Clinic, Phoenix, AZ, USA.
Catherine Daniela ChongDepartment of Neurology, Mayo Clinic, Phoenix, AZ, USA.ORCID 0000-0002-9035-8748
Gina M DumkriegerDepartment of Neurology, Mayo Clinic, Phoenix, AZ, USA.ORCID 0000-0001-9519-5370
Jing LiGeorgia Tech, School of Industrial and Systems Engineering, Georgia, USA.
Teresa WuASU-Mayo Center for Innovative Imaging, Tempe, AZ, USA.
Todd J SchwedtDepartment of Neurology, Mayo Clinic, Phoenix, AZ, USA.
Mayo Clinic Hospital · USAdvanced Imaging Research (United States) · USGeorgia Institute of Technology · US

Funding

Biomarker Signature to Predict the Persistence of Post-Traumatic HeadacheR61NS113315 · NINDS · MAYO CLINIC ARIZONA · PI CHONG, CATHERINE DANIELA · 2019 to 2019
$3.2M
Biomarker Signature to Predict the Persistence of Post-Traumatic HeadacheR33NS113315 · NINDS · MAYO CLINIC ARIZONA · PI CHONG, CATHERINE DANIELA · 2023 to 2024
$2.1M
NINDS NIH HHS R33 NS113315NINDS NIH HHS R61 NS113315
6 · The paper itself

Abstract

objectivesThe objective of this longitudinal study was to determine whether brain iron accumulation, measured using magnetic resonance imaging magnetic transverse relaxation rates (T2*), is associated with response to erenumab for the treatment of migraine.

methodsParticipants (n = 28) with migraine, diagnosed using international classification of headache disorders 3rd edition criteria, were eligible if they had six to 25 migraine days during a four-week headache diary run-in phase. Participants received two treatments with 140 mg erenumab, one immediately following the pre-treatment run-in phase and a second treatment four weeks later. T2* data were collected immediately following the pre-treatment phase, and at two weeks and eight weeks following the first erenumab treatment. Patients were classified as erenumab responders if their migraine-day frequency at five-to-eight weeks post-initial treatment was reduced by at least 50% compared to the pre-treatment run-in phase. A longitudinal Sandwich estimator approach was used to compare longitudinal group differences (responders vs non-responders) in T2* values, associated with iron accumulation. Group visit effects were calculated with a significance threshold of p = 0.005 and cluster forming threshold of 250 voxels. T2* values of 19 healthy controls were used for a reference. The average of each significant region was compared between groups and visits with Bonferroni corrections for multiple comparisons with significance defined as p < 0.05.

resultsPre- and post-treatment longitudinal imaging data were available from 28 participants with migraine for a total of 79 quantitative T2* images. Average subject age was 42 ± 13 years (25 female, three male). Of the 28 subjects studied, 53.6% were erenumab responders. Comparing longitudinal T2* between erenumab responders vs non-responders yielded two comparisons which survived the significance threshold of p < 0.05 after correction for multiple comparisons: the difference at eight weeks between the erenumab-responders and non-responders in the periaqueductal gray (mean ± standard error; responders 43 ± 1 ms vs non-responders 32.5 ± 1 ms, p = 0.002) and the anterior cingulate cortex (mean ± standard error; responders 50 ± 1 ms vs non-responders 40 ± 1 ms, p = 0.01).

conclusionsErenumab response is associated with higher T2* in the periaqueductal gray and anterior cingulate cortex, regions that participate in pain processing and modulation. T2* differences between erenumab responders vs non-responders, a measure of brain iron accumulation, are seen at eight weeks post-treatment. Less iron accumulation in the periaqueductal gray and anterior cingulate cortex might play a role in the therapeutic mechanisms of migraine reduction associated with erenumab.

Indexed as

Migraine DisordersPeriaqueductal GrayAdultAntibodies, Monoclonal, HumanizedFemaleGyrus CinguliHumansIronLongitudinal StudiesMaleMiddle AgedTreatment OutcomeAntibodies, Monoclonal, HumanizederenumabIroncalcitonin gene-related peptideerenumabironmagnetic resonance imagingMigraineT2*

Identifiers

PMID36756979
PMCPMC10316773
OpenAlexW4319656140

What OpenQuestion holds

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LicenceCC BY-NC
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.