Neurophysiology of Cerebellar Ataxias and Gait Disorders
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There are numerous forms of cerebellar disorders from sporadic to genetic diseases. The aim of this chapter is to provide an overview of the advances and emerging techniques during these last 2 decades in the neurophysiological tests useful in cerebellar patients for clinical and research purposes. Clinically, patients exhibit various combinations of a vestibulocerebellar syndrome, a cerebellar cognitive affective syndrome and a cerebellar motor syndrome which will be discussed throughout this chapter. Cerebellar patients show abnormal Bereitschaftpotentials (BPs) and mismatch negativity. Cerebellar EEG is now being applied in cerebellar disorders to unravel impaired electrophysiological patterns associated within disorders of the cerebellar cortex. Eyeblink conditioning is significantly impaired in cerebellar disorders: the ability to acquire conditioned eyeblink responses is reduced in hereditary ataxias, in cerebellar stroke and after tumor surgery of the cerebellum. Furthermore, impaired eyeblink conditioning is an early marker of cerebellar degenerative disease. General rules of motor control suggest that optimal strategies are needed to execute voluntary movements in the complex environment of daily life. A high degree of adaptability is required for learning procedures underlying motor control as sensorimotor adaptation is essential to perform accurate goal-directed movements. Cerebellar patients show impairments during online visuomotor adaptation tasks. Cerebellum-motor cortex inhibition (CBI) is a neurophysiological biomarker showing an inverse association between cerebellothalamocortical tract integrity and ataxia severity. Ataxic gait is characterized by increased step width, reduced ankle joint range of motion, increased gait variability, lack of intra-limb inter-joint and inter-segmental coordination, impaired foot ground placement and loss of trunk control. Taken together, these techniques provide a neurophysiological framework for a better appraisal of cerebellar disorders.
Lurcher Mouse as a Model of Cerebellar Syndromes.
Roy Choudhury N, Hilber P, Cendelin J Cerebellum. 2025; 24(2):54.
PMID: 40016581 PMC: 11868327. DOI: 10.1007/s12311-025-01810-5.
Castiglia S, Sebastianelli G, Abagnale C, Casillo F, Trabassi D, Di Lorenzo C Sensors (Basel). 2024; 24(23).
PMID: 39686163 PMC: 11644986. DOI: 10.3390/s24237627.
At-home wearables and machine learning capture motor impairment and progression in adult ataxias.
Manohar R, Yang F, Stephen C, Schmahmann J, Eklund N, Gupta A medRxiv. 2024; .
PMID: 39574866 PMC: 11581084. DOI: 10.1101/2024.10.27.24316161.
Trabassi D, Castiglia S, Bini F, Marinozzi F, Ajoudani A, Lorenzini M Sensors (Basel). 2024; 24(11).
PMID: 38894404 PMC: 11175240. DOI: 10.3390/s24113613.
SCAR32: Functional characterization and expansion of the clinical-genetic spectrum.
Naef V, Lieto M, Satolli S, De Micco R, Troisi M, Pasquariello R Ann Clin Transl Neurol. 2024; 11(7):1879-1886.
PMID: 38837640 PMC: 11251466. DOI: 10.1002/acn3.52094.