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Long-term evolution of white and gray matter structural properties in migraine
Álvaro Planchuelo-Gómez1, Carmen Martín-Martín1, Ángel L Guerrero2,3
1Image Processing Laboratory, Universidad de Valladolid, Valladolid, Spain.
Headache
|May 9, 2025
Summary
Migraine brain structure changes over time, differing by clinical course. Stable diagnoses showed maladaptation in pain regions, while improved chronic migraine patients had distinct white matter changes.
Area of Science:
- Neuroimaging
- Neurology
- Migraine Research
Background:
- Previous studies identified gray matter (GM) and white matter (WM) differences between chronic migraine (CM) and episodic migraine (EM).
- Specific GM changes in CM include increased cortical thickness and reduced surface area in various brain regions.
- WM alterations in CM involve widespread reduced diffusivity in key white matter tracts.
Purpose of the Study:
- To investigate longitudinal brain structural changes in migraine patients.
- To correlate these changes with distinct clinical diagnoses and temporal disease progression.
- To understand the evolution of GM and WM differences over an extended period.
Main Methods:
- Longitudinal cohort study using brain MRI (T1- and diffusion-weighted) at two timepoints.
- Analysis of three WM descriptors and four GM morphometry parameters.
- Generalized linear mixed models used to analyze longitudinal changes in stable EM (31), stable CM (24), and improved CM to EM (24) groups.
Main Results:
- Stable EM patients showed longitudinal cortical thickness increases in parietal and temporal regions.
- Stable CM and EM patients exhibited longitudinal cortical thickness decreases in the posterior cingulate gyrus.
- Stable EM patients demonstrated a longitudinal increase in fractional anisotropy in the cerebral peduncle.
Conclusions:
- Clinical evolution in migraine is associated with distinct patterns of structural brain changes.
- Migraine patients who improved from CM to EM showed no significant GM changes.
- Longitudinally stable migraine patients displayed maladaptation in pain processing regions and adaptation in other areas.

