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Task-dependent deterioration of balance underpinning cognitive-postural interference in MS.

Identifieur interne : 000633 ( Main/Corpus ); précédent : 000632; suivant : 000634

Task-dependent deterioration of balance underpinning cognitive-postural interference in MS.

Auteurs : Luca Prosperini ; Letizia Castelli ; Francesca De Luca ; Francesca Fabiano ; Ilaria Ferrante ; Laura De Giglio

Source :

RBID : pubmed:27521436

English descriptors

Abstract

OBJECTIVE

To investigate which concurrent cognitive task (if any) had the most detrimental effect on balance control of patients with multiple sclerosis (MS).

METHODS

In a dual-task experiment, we evaluated the reciprocal effect of simultaneously performing a postural and a cognitive task on balance and cognition in 52 patients and 26 sex- and age-matched controls. Balance was assessed by static posturography, while cognition was scored as number of correct items at 3 different neuropsychological tests, i.e., the Symbol Digit Modalities Test (SDMT), word list generation (WLG), and Stroop Color-Word Test (SCWT).

RESULTS

In both single and dual-task conditions, the patients had larger postural sway and worse scores at SDMT, WLG, and SCWT than the controls (p < 0.05). Test-retest reliability was excellent for all dual-task metrics (85%-94%). By means of 2-way analyses of the variance, we found significant main effects of dual task on balance, regardless of the concurrent cognitive task (p < 0.001). There was no main effect of dual task on cognitive performance across all the 3 task conditions (p ≥ 0.1). We observed a significant condition-by-group interaction effect on balance only when the SCWT was administered as concurrent task (p = 0.01), indicating a greater dual-task cost of balance for the patients than controls (53% vs 28%, p = 0.04).

CONCLUSIONS

We suggest that tasks exploring executive functions involved in discriminating conflicting stimuli may be the most suitable to unmask the cognitive-postural interference phenomenon in patients with MS. This may support the hypothesis that MS-related damage constrains brain networks to subserve both postural control and executive functions.


DOI: 10.1212/WNL.0000000000003090
PubMed: 27521436

Links to Exploration step

pubmed:27521436

Le document en format XML

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<name sortKey="Prosperini, Luca" sort="Prosperini, Luca" uniqKey="Prosperini L" first="Luca" last="Prosperini">Luca Prosperini</name>
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<nlm:affiliation>From the Department of Neurology and Psychiatry, Sapienza University, Rome, Italy. luca.prosperini@uniroma1.it.</nlm:affiliation>
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<name sortKey="Castelli, Letizia" sort="Castelli, Letizia" uniqKey="Castelli L" first="Letizia" last="Castelli">Letizia Castelli</name>
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<nlm:affiliation>From the Department of Neurology and Psychiatry, Sapienza University, Rome, Italy.</nlm:affiliation>
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<name sortKey="De Luca, Francesca" sort="De Luca, Francesca" uniqKey="De Luca F" first="Francesca" last="De Luca">Francesca De Luca</name>
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<nlm:affiliation>From the Department of Neurology and Psychiatry, Sapienza University, Rome, Italy.</nlm:affiliation>
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<name sortKey="Fabiano, Francesca" sort="Fabiano, Francesca" uniqKey="Fabiano F" first="Francesca" last="Fabiano">Francesca Fabiano</name>
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<nlm:affiliation>From the Department of Neurology and Psychiatry, Sapienza University, Rome, Italy.</nlm:affiliation>
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<name sortKey="Ferrante, Ilaria" sort="Ferrante, Ilaria" uniqKey="Ferrante I" first="Ilaria" last="Ferrante">Ilaria Ferrante</name>
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<name sortKey="De Giglio, Laura" sort="De Giglio, Laura" uniqKey="De Giglio L" first="Laura" last="De Giglio">Laura De Giglio</name>
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<name sortKey="Ferrante, Ilaria" sort="Ferrante, Ilaria" uniqKey="Ferrante I" first="Ilaria" last="Ferrante">Ilaria Ferrante</name>
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<term>Executive Function (MeSH)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Motor Activity (MeSH)</term>
<term>Multiple Sclerosis (physiopathology)</term>
<term>Multiple Sclerosis (psychology)</term>
<term>Neuropsychological Tests (MeSH)</term>
<term>Postural Balance (MeSH)</term>
<term>Reproducibility of Results (MeSH)</term>
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<p>
<b>OBJECTIVE</b>
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<p>To investigate which concurrent cognitive task (if any) had the most detrimental effect on balance control of patients with multiple sclerosis (MS).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>In a dual-task experiment, we evaluated the reciprocal effect of simultaneously performing a postural and a cognitive task on balance and cognition in 52 patients and 26 sex- and age-matched controls. Balance was assessed by static posturography, while cognition was scored as number of correct items at 3 different neuropsychological tests, i.e., the Symbol Digit Modalities Test (SDMT), word list generation (WLG), and Stroop Color-Word Test (SCWT).</p>
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<p>
<b>RESULTS</b>
</p>
<p>In both single and dual-task conditions, the patients had larger postural sway and worse scores at SDMT, WLG, and SCWT than the controls (p < 0.05). Test-retest reliability was excellent for all dual-task metrics (85%-94%). By means of 2-way analyses of the variance, we found significant main effects of dual task on balance, regardless of the concurrent cognitive task (p < 0.001). There was no main effect of dual task on cognitive performance across all the 3 task conditions (p ≥ 0.1). We observed a significant condition-by-group interaction effect on balance only when the SCWT was administered as concurrent task (p = 0.01), indicating a greater dual-task cost of balance for the patients than controls (53% vs 28%, p = 0.04).</p>
</div>
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<p>
<b>CONCLUSIONS</b>
</p>
<p>We suggest that tasks exploring executive functions involved in discriminating conflicting stimuli may be the most suitable to unmask the cognitive-postural interference phenomenon in patients with MS. This may support the hypothesis that MS-related damage constrains brain networks to subserve both postural control and executive functions.</p>
</div>
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<CopyrightInformation>© 2016 American Academy of Neurology.</CopyrightInformation>
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