Javascript must be enabled to continue!
Does abnormal interhemispheric inhibition play a role in mirror dystonia?
View through CrossRef
AbstractThe presence of mirror dystonia (dystonic movement induced by a specific task performed by the unaffected hand) in the dominant hand of writer's cramp patients when the nondominant hand is moved suggests an abnormal interaction between the 2 hemispheres. In this study we compare the level of interhemispheric inhibition (IHI) in 2 groups of patients with writer's cramp, one with the presence of a mirror dystonia and the other without as well as a control group. The level of bidirectional IHI was measured in wrist muscles with dual‐site transcranial magnetic stimulation with a 10‐millisecond (short IHI) and a 40‐millisecond (long IHI) interstimulus interval during rest and while holding a pen in 9 patients with mirror dystonia 7 without mirror dystonia, and 13 controls. The group of patients without mirror dystonia did not differ from the controls in their IHI level. In contrast, IHI was significantly decreased in the group of patients with mirror dystonia in comparison with the group without mirror dystonia and the controls in both wrist muscles of both the dystonic and unaffected hand whatever the resting or active condition (P = 0.001). The decrease of IHI level in the group of patients with mirror dystonia was negatively correlated with the severity and the duration of the disease: the weaker the level of IHI, the more severe was the disease and the longer its duration. Interhemispheric inhibition disturbances are most likely involved in the occurrence of mirror dystonia. This bilateral deficient inhibition further suggests the involvement of the unaffected hemisphere in the pathophysiology of unilateral dystonia. © 2013 International Parkinson and Movement Disorder Society
Title: Does abnormal interhemispheric inhibition play a role in mirror dystonia?
Description:
AbstractThe presence of mirror dystonia (dystonic movement induced by a specific task performed by the unaffected hand) in the dominant hand of writer's cramp patients when the nondominant hand is moved suggests an abnormal interaction between the 2 hemispheres.
In this study we compare the level of interhemispheric inhibition (IHI) in 2 groups of patients with writer's cramp, one with the presence of a mirror dystonia and the other without as well as a control group.
The level of bidirectional IHI was measured in wrist muscles with dual‐site transcranial magnetic stimulation with a 10‐millisecond (short IHI) and a 40‐millisecond (long IHI) interstimulus interval during rest and while holding a pen in 9 patients with mirror dystonia 7 without mirror dystonia, and 13 controls.
The group of patients without mirror dystonia did not differ from the controls in their IHI level.
In contrast, IHI was significantly decreased in the group of patients with mirror dystonia in comparison with the group without mirror dystonia and the controls in both wrist muscles of both the dystonic and unaffected hand whatever the resting or active condition (P = 0.
001).
The decrease of IHI level in the group of patients with mirror dystonia was negatively correlated with the severity and the duration of the disease: the weaker the level of IHI, the more severe was the disease and the longer its duration.
Interhemispheric inhibition disturbances are most likely involved in the occurrence of mirror dystonia.
This bilateral deficient inhibition further suggests the involvement of the unaffected hemisphere in the pathophysiology of unilateral dystonia.
© 2013 International Parkinson and Movement Disorder Society.
Related Results
Efficacy and Safety of Zolpidem for Focal Dystonia After Neurosurgical Treatments: A Retrospective Cohort Study
Efficacy and Safety of Zolpidem for Focal Dystonia After Neurosurgical Treatments: A Retrospective Cohort Study
Although there are several reports of the significant efficacy of zolpidem for treating dystonia, zolpidem is still considered an anecdotal treatment. Here, we evaluated the effica...
Decoding Dystonia in Autoimmune Disorders: A Scoping Review
Decoding Dystonia in Autoimmune Disorders: A Scoping Review
Background: Dystonia is a common hyperkinetic movement disorder observed in various genetic, infective, drug-induced, and autoimmune disorders. Autoimmune disorders can present wit...
Rare Variant Burden in Known Dystonia Genes in Population Controls and Sporadic Dystonia Patients
Rare Variant Burden in Known Dystonia Genes in Population Controls and Sporadic Dystonia Patients
Abstract
Background
Rare mutations in genes associated with Mendelian forms of disease are a potential mechanism for sporadic d...
Clinical Presentation and Evolution of Isolated Focal and Segmental Dystonia in Adults – 20 Years’ Experience from a Botulinum Toxin Clinic
Clinical Presentation and Evolution of Isolated Focal and Segmental Dystonia in Adults – 20 Years’ Experience from a Botulinum Toxin Clinic
Background and Objectives:
Isolated dystonia generally occurs due to genetic causes, and the pattern and distribution may change over time. Botulinum toxin is t...
Cometary Physics Laboratory: spectrophotometric experiments
Cometary Physics Laboratory: spectrophotometric experiments
<p><strong><span dir="ltr" role="presentation">1. Introduction</span></strong&...
Potential Interactions Between Cerebellar Dysfunction and Sleep Disturbances in Dystonia
Potential Interactions Between Cerebellar Dysfunction and Sleep Disturbances in Dystonia
Dystonia is the third most common movement disorder. It causes debilitating twisting postures that are accompanied by repetitive and sometimes intermittent co- or over-contractions...
Physician Approaches to the Pharmacologic Treatment of Dystonia in Cerebral Palsy
Physician Approaches to the Pharmacologic Treatment of Dystonia in Cerebral Palsy
Abstract
Objective
To determine how physicians approach pharmacologic dystonia treatment in people with CP and assess physician...
Spectrum of Dystonia in Spinocerebellar Ataxia
Spectrum of Dystonia in Spinocerebellar Ataxia
Background: Spinocerebellar ataxias (SCAs) are a diverse group of inherited disorders characterized by progressive cerebellar dysfunction. Beyond the classic ataxic features, dysto...

