Abstract

Various etiopathologies affect the cerebellum, resulting in the development of cerebellar ataxias (CAs), a heterogeneous group of disorders characterized clinically by movement incoordination, affective dysregulation, and cognitive dysmetria. Recent progress in clinical and basic research has opened the door of the ‘‘era of therapy” of CAs. The therapeutic rationale of cerebellar diseases takes into account the capacity of the cerebellum to compensate for pathology and restoration, which is collectively termed cerebellar reserve. In general, treatments of CAs are classified into two categories: cause-cure treatments, aimed at arresting disease progression, and neuromodulation therapies, aimed at potentiating cerebellar reserve. Both forms of therapies should be introduced as soon as possible, at a time where cerebellar reserve is still preserved. Clinical studies have established evidence-based cause-cure treatments for metabolic and immune-mediated CAs. Elaborate protocols of rehabilitation and non-invasive cerebellar stimulation facilitate cerebellar reserve, leading to recovery in the case of controllable pathologies (metabolic and immune-mediated CAs) and delay of disease progression in the case of uncontrollable pathologies (degenerative CAs). Furthermore, recent advances in molecular biology have encouraged the development of new forms of therapies: the molecular targeting therapy, which manipulates impaired RNA or proteins, and the neurotransplantation therapy, which delays cell degeneration and facilitates compensatory functions. The present review focuses on the therapeutic rationales of these recently developed therapeutic modalities, highlighting the underlying pathogenesis.

Highlights

  • Cerebellar ataxias (CAs) encompass a heterogeneous group of disorders characterized by motor incoordination, affective impairment, and disorganized cognitive operations resulting in dysmetria of thought [1,2]

  • The cerebellum is endowed with the capacity to compensate and restore damage inflicted by various pathologies, a specific feature in the Central Nervous System (CNS) [4,7]

  • Strictly speaking, it should be acknowledged that the rehabilitation programs designed for patients with cerebral disorders cannot be applied in patients with Schmahmann syndrome [78]

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Summary

History

Cerebellar ataxias (CAs) encompass a heterogeneous group of disorders characterized by motor incoordination, affective impairment, and disorganized cognitive operations resulting in dysmetria of thought [1,2]. Evidence-based therapeutic strategies have been established for metabolic and immune-mediated CAs. Improved protocols have been proposed in the field of rehabilitation to reconstruct or compensate lost cerebellar functions. Typical examples are molecular targeting therapies designed to manipulate RNAs or key proteins and the transplantation of grafted stem cells to facilitate the reversibility of host cells. These clinical and basic advances have opened the door to a new era where neuroscientists and clinicians will control the process of cell death and restore impaired cerebellar functions [5,6]. The aim of the present review is to assess the newly established therapeutic methods and anti-ataxic drugs

Therapeutic Strategies Based on Cerebellar Reserve
Alcohol-Related Cerebellar Ataxias
Iron Deposition
Immune-Mediated CAs
Anti-GAD Ataxia
Abetalipoproteinemia
GLUT1 Deficiency
Motor Rehabilitation
Cognitive Rehabilitation
Non-Invasive Cerebellar Stimulation
Novel Therapies
Polyglutaminopathies
ADCAs Induced by Toxic RNAs
ADCAs Caused by Point Mutations
Therapeutic Rationale
Possible Indications for Neurotransplantation
Findings
Conclusions
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