Patients with chronic migraine without history of medication overuse are characterized by a peculiar white matter fiber bundle profile.


Journal

The journal of headache and pain
ISSN: 1129-2377
Titre abrégé: J Headache Pain
Pays: England
ID NLM: 100940562

Informations de publication

Date de publication:
18 Jul 2020
Historique:
received: 05 06 2020
accepted: 13 07 2020
entrez: 20 7 2020
pubmed: 20 7 2020
medline: 3 11 2020
Statut: epublish

Résumé

We investigated intracerebral fiber bundles using a tract-based spatial statistics (TBSS) analysis of diffusion tensor imaging (DTI) data to verify microstructural integrity in patients with episodic (MO) and chronic migraine (CM). We performed DTI in 19 patients with MO within interictal periods, 18 patients with CM without any history of drug abuse, and 18 healthy controls (HCs) using a 3 T magnetic resonance imaging scanner. We calculated diffusion metrics, including fractional anisotropy (FA), axial diffusion (AD), radial diffusion (RD), and mean diffusion (MD). TBSS revealed no significant differences in the FA, MD, RD, and AD maps between the MO and HC groups. In comparison to the HC group, the CM group exhibited widespread increased RD (bilateral superior [SCR] and posterior corona radiata [PCR], bilateral genu of the corpus callosum [CC], bilateral posterior limb of internal capsule [IC], bilateral superior longitudinal fasciculus [LF]) and MD values (tracts of the right SCR and PCR, right superior LF, and right splenium of the CC). In comparison to the MO group, the CM group showed decreased FA (bilateral SCR and PCR, bilateral body of CC, right superior LF, right forceps minor) and increased MD values (bilateral SCR and right PCR, right body of CC, right superior LF, right splenium of CC, and right posterior limb of IC). Our results suggest that chronic migraine can be associated with the widespread disruption of normal white matter integrity in the brain.

Sections du résumé

BACKGROUND BACKGROUND
We investigated intracerebral fiber bundles using a tract-based spatial statistics (TBSS) analysis of diffusion tensor imaging (DTI) data to verify microstructural integrity in patients with episodic (MO) and chronic migraine (CM).
METHODS METHODS
We performed DTI in 19 patients with MO within interictal periods, 18 patients with CM without any history of drug abuse, and 18 healthy controls (HCs) using a 3 T magnetic resonance imaging scanner. We calculated diffusion metrics, including fractional anisotropy (FA), axial diffusion (AD), radial diffusion (RD), and mean diffusion (MD).
RESULTS RESULTS
TBSS revealed no significant differences in the FA, MD, RD, and AD maps between the MO and HC groups. In comparison to the HC group, the CM group exhibited widespread increased RD (bilateral superior [SCR] and posterior corona radiata [PCR], bilateral genu of the corpus callosum [CC], bilateral posterior limb of internal capsule [IC], bilateral superior longitudinal fasciculus [LF]) and MD values (tracts of the right SCR and PCR, right superior LF, and right splenium of the CC). In comparison to the MO group, the CM group showed decreased FA (bilateral SCR and PCR, bilateral body of CC, right superior LF, right forceps minor) and increased MD values (bilateral SCR and right PCR, right body of CC, right superior LF, right splenium of CC, and right posterior limb of IC).
CONCLUSION CONCLUSIONS
Our results suggest that chronic migraine can be associated with the widespread disruption of normal white matter integrity in the brain.

Identifiants

pubmed: 32682393
doi: 10.1186/s10194-020-01159-6
pii: 10.1186/s10194-020-01159-6
pmc: PMC7368770
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

92

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Auteurs

Gianluca Coppola (G)

Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome Polo Pontino, Latina, Italy.

Antonio Di Renzo (A)

IRCCS - Fondazione Bietti, Research Unit of Neurophysiology of Vision and Neuro-Ophthalmology, Via Livenza 3, 00198, Rome, Italy.

Emanuele Tinelli (E)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Barbara Petolicchio (B)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Cherubino Di Lorenzo (C)

Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome Polo Pontino, Latina, Italy.

Vincenzo Parisi (V)

IRCCS - Fondazione Bietti, Research Unit of Neurophysiology of Vision and Neuro-Ophthalmology, Via Livenza 3, 00198, Rome, Italy. vincenzo.parisi@fondazionebietti.it.

Mariano Serrao (M)

Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome Polo Pontino, Latina, Italy.

Valentina Calistri (V)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Stefano Tardioli (S)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Gaia Cartocci (G)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Francesca Caramia (F)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Vittorio Di Piero (V)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Francesco Pierelli (F)

Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome Polo Pontino, Latina, Italy.
IRCCS - Neuromed, Pozzilli, IS, Italy.

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Classifications MeSH