Brain network topology and future development of freezing of gait in Parkinson’s disease: a longitudinal study

• Published in: Journal of neurology Vol. 269; no. 5; pp. 2503 - 2512
• Main Authors: Li, Nannan, Lei, Du, Peng, Jiaxin, Suo, Xueling, Li, Junying, Duan, Liren, Chen, Chaolan, Gong, Qiyong, Peng, Rong
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.05.2022; Springer Nature B.V
• Subjects: Brain - diagnostic imaging; Brain architecture; Cerebellum; Comparative analysis; Cortex (frontal); Frontal gyrus; Functional morphology; Gait; Gait Disorders, Neurologic - complications; Gait Disorders, Neurologic - etiology; Humans; Latency; Longitudinal Studies; Magnetic Resonance Imaging; Medicine; Medicine & Public Health; Movement disorders; Neurodegenerative diseases; Neurology; Neuroradiology; Neurosciences; Occipital lobe; Original Communication; Parkinson Disease - complications; Parkinson Disease - diagnostic imaging; Parkinson's disease; Visual cortex; Freezing of gait; Graph theory; Magnetic resonance imaging; Brain networks; Parkinson’s disease
• ISSN: 0340-5354; 1432-1459; 1432-1459
• DOI: 10.1007/s00415-021-10817-x

Background Freezing of gait (FOG) is a common disabling gait disturbance in Parkinson’s disease (PD). The objectives of this study were to explore alterations in the topological organization of whole-brain functional networks in patients with PD who will develop FOG. Methods We recruited 20 patients with PD who developed FOG (PD-FOGt) during a 5-year follow-up period, 20 patients with PD who did not developed FOG (PD-FOGn) within the follow-up period, and 20 healthy control subjects. Using graph theory approaches, we performed a comparative analysis of the topological organization of whole-brain functional networks among the groups, and further explored their potential relationships with latency to develop FOG. Results At baseline, the global topological properties of functional brain networks in PD-FOGt and PD-FOGn showed no abnormalities. Additionally, regarding regional topological properties, compared with PD-FOGn patients, PD-FOGt patients exhibited decreased nodal centrality in the left middle frontal gyrus (MFG). Although there were no significant differences compared with PD-FOGn patients, the PD-FOGt group exhibited the lowest nodal centrality values in the frontal cortex (left gyrus rectus), and visual cortex (bilateral inferior occipital gyrus and left fusiform gyrus), and the highest nodal centrality values in the cerebellum (vermis_6) among the three groups. However, no relationship was found between the nodal centrality in above brain regions and latency to develop FOG. Conclusion This study demonstrates the disrupted regional topological organization might contribute to the future development of FOG in PD patients, especially associated with damage to the left MFG.