TY - JOUR
T1 - Psychiatric phenotype in neurodevelopmental myoclonus-dystonia is underpinned by abnormality of cerebellar modulation on the cerebral cortex
AU - Tarrano, Clément
AU - Galléa, Cécile
AU - Delorme, Cécile
AU - McGovern, Eavan M
AU - Atkinson-Clement, Cyril
AU - Brochard, Vanessa
AU - Thobois, Stéphane
AU - Tranchant, Christine
AU - Grabli, David
AU - Degos, Bertrand
AU - Corvol, Jean Christophe
AU - Pedespan, Jean-Michel
AU - Krystkowiak, Pierre
AU - Houeto, Jean-Luc
AU - Degardin, Adrian
AU - Defebvre, Luc
AU - Beranger, Benoit
AU - Martino, Davide
AU - Apartis, Emmanuelle
AU - Vidailhet, Marie
AU - Roze, Emmanuel
AU - Worbe, Yulia
N1 - © 2024. The Author(s).
PY - 2024/9/27
Y1 - 2024/9/27
N2 - Psychiatric symptoms are common in neurodevelopmental movement disorders, including some types of dystonia. However, research has mainly focused on motor manifestations and underlying circuits. Myoclonus-dystonia is a rare and homogeneous neurodevelopmental condition serving as an illustrative paradigm of childhood-onset dystonias, associated with psychiatric symptoms. Here, we assessed the prevalence of psychiatric disorders and the severity of depressive symptoms in patients with myoclonus-dystonia and healthy volunteers (HV). Using resting-state functional neuroimaging, we compared the effective connectivity within and among non-motor and motor brain networks between patients and HV. We further explored the hierarchical organization of these networks and examined the relationship between their connectivity and the depressive symptoms. Comparing 19 patients to 25 HV, we found a higher prevalence of anxiety disorders and more depressive symptoms in the patient group. Patients exhibited abnormal modulation of the cerebellum on the cerebral cortex in the sensorimotor, dorsal attention, salience, and default mode networks. Moreover, the salience network activity was directed by the cerebellum in patients and was related to depressive symptoms. Altogether, our findings highlight the role of the cerebellar drive on both motor and non-motor cortical areas in this disorder, suggesting cerebellar involvement in the complex phenotype of such neurodevelopmental movement disorders.
AB - Psychiatric symptoms are common in neurodevelopmental movement disorders, including some types of dystonia. However, research has mainly focused on motor manifestations and underlying circuits. Myoclonus-dystonia is a rare and homogeneous neurodevelopmental condition serving as an illustrative paradigm of childhood-onset dystonias, associated with psychiatric symptoms. Here, we assessed the prevalence of psychiatric disorders and the severity of depressive symptoms in patients with myoclonus-dystonia and healthy volunteers (HV). Using resting-state functional neuroimaging, we compared the effective connectivity within and among non-motor and motor brain networks between patients and HV. We further explored the hierarchical organization of these networks and examined the relationship between their connectivity and the depressive symptoms. Comparing 19 patients to 25 HV, we found a higher prevalence of anxiety disorders and more depressive symptoms in the patient group. Patients exhibited abnormal modulation of the cerebellum on the cerebral cortex in the sensorimotor, dorsal attention, salience, and default mode networks. Moreover, the salience network activity was directed by the cerebellum in patients and was related to depressive symptoms. Altogether, our findings highlight the role of the cerebellar drive on both motor and non-motor cortical areas in this disorder, suggesting cerebellar involvement in the complex phenotype of such neurodevelopmental movement disorders.
KW - Humans
KW - Male
KW - Female
KW - Cerebellum/physiopathology
KW - Dystonic Disorders/physiopathology
KW - Cerebral Cortex/physiopathology
KW - Adult
KW - Phenotype
KW - Depression/physiopathology
KW - Young Adult
KW - Magnetic Resonance Imaging
KW - Adolescent
KW - Neurodevelopmental Disorders/physiopathology
U2 - 10.1038/s41598-024-73386-9
DO - 10.1038/s41598-024-73386-9
M3 - Article
C2 - 39333780
SN - 2045-2322
VL - 14
SP - 22341
JO - Scientific Reports
JF - Scientific Reports
IS - 1
ER -