Impaired glymphatic function and advanced brain age gap in chronic migraine: a multimodal MRI study.
Authors
Affiliations (8)
Affiliations (8)
- Department of Neurology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, 325027, China.
- Wenzhou Key Laboratory of Neurogenetics, Wenzhou, Zhejiang, 325027, China.
- Department of Radiology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, 325027, China.
- Wenzhou Key Laboratory of Structural and Functional Imaging, Wenzhou, Zhejiang, 325027, China.
- Department of Radiology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, 325027, China. [email protected].
- Wenzhou Key Laboratory of Structural and Functional Imaging, Wenzhou, Zhejiang, 325027, China. [email protected].
- Department of Neurology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, 325027, China. [email protected].
- Wenzhou Key Laboratory of Neurogenetics, Wenzhou, Zhejiang, 325027, China. [email protected].
Abstract
This study investigated whether the coupling between cortical blood-oxygen-level-dependent (BOLD) signals and cerebrospinal fluid (CSF) flow, a physiologically motivated but indirect proxy related to glymphatic-associated dynamics, moderates the relationship between migraine disability (MIDAS) and brain age gap (BAG). Patients with episodic migraine (EM), chronic migraine (CM), and healthy controls were recruited. BAG was estimated using a deep learning-based framework, and glymphatic-related hemodynamic-CSF dynamics were assessed using BOLD-CSF coupling. A moderation model, adjusted for sleep quality (PSQI) and biological covariates using HC3 robust standard errors, evaluated the statistical moderating role of BOLD-CSF coupling on the MIDAS-BAG association. A network-specific pattern of altered BOLD-CSF coupling was identified, with higher-order network abnormalities observed specifically in CM (p = 0.037). CM patients exhibited a significantly greater BAG than EM patients and healthy controls (p = 0.007). BOLD-CSF coupling significantly moderated the association between MIDAS and BAG (interaction β = -0.104, p = 0.035; Wald test p = 0.036). In individuals with relatively stronger coupling, MIDAS was more strongly associated with BAG (β = 0.066, p < 0.001), whereas this association was attenuated in those with weaker coupling (β = 0.035, p = 0.005). Altered higher-order network BOLD-CSF coupling may represent a relevant imaging feature of migraine chronification. BOLD-CSF coupling was associated with interindividual differences in the relationship between migraine-related disability and BAG, independent of sleep quality. These findings support the potential relevance of glymphatic-related physiological processes in chronic migraine.