Dysfunctional mesocorticolimbic circuitry in cluster headache

Background This study aimed to identify mesocorticolimbic functional abnormalities in cluster headache (CH) patients, disentangling the roles of chronification and affective symptoms. Methods Using the monetary incentive delay fMRI task to directly engage these pathways, we investigated functional a...

Full description

Saved in:
Bibliographic Details
Published inJournal of headache and pain Vol. 26; no. 1; pp. 121 - 16
Main Authors Ferraro, Stefania, Demichelis, Greta, Medina Carrion, Jean Paul, Liu, Dan, Becker, Benjamin, Maes, Michael, Fedeli, Davide, Ciullo, Giuseppe, Usai, Susanna, Grisoli, Marina, Chiapparini, Luisa, Cecchini Proietti, Alberto, Giani, Luca, Nigri, Anna, Leone, Massimo
Format Journal Article
LanguageEnglish
Published Milan Springer Milan 19.05.2025
Springer Nature B.V
BMC
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background This study aimed to identify mesocorticolimbic functional abnormalities in cluster headache (CH) patients, disentangling the roles of chronification and affective symptoms. Methods Using the monetary incentive delay fMRI task to directly engage these pathways, we investigated functional alterations in key regions of this network in chronic ( n  = 23) and episodic CH patients ( n  = 49) compared to a control group ( n  = 32). After processing the fMRI data, we extracted beta values from selected regions and for contrasts of interest and entered them into logistic regression models adjusted for potential confounders (such as depressive and anxiety symptoms and smoking habit) to test their association with the diagnoses (chronic CH and control subjects, episodic CH and control subjects). Results Results showed that chronic CH patients exhibited reduced ventral tegmental area (VTA) activity and a tendency towards significance ( p  = 0.056) for an increased medial prefrontal cortex (mPFC) responsiveness during reward anticipation, alongside a significant decrease in mPFC activity during reward outcomes. Episodic patients displayed abnormal mPFC activity across both reward phases, but coupled with intact VTA responses. Importantly, these functional abnormalities were not correlated to depressive and anxiety symptoms and smoking habits. Conclusions These findings suggest that chronic CH patients experience an imbalance in the VTA-mPFC pathway, while episodic patients may show early signs of this emerging dysfunction. Moreover, the observed reward processing alterations seem distinct from those associated with affective disorders, possibly highlighting unique mechanisms underlying the pathophysiology of CH.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:1129-2377
1129-2369
1129-2377
DOI:10.1186/s10194-025-02017-z