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Postural imbalance and falls in PSP correlate with functional pathology of the thalamus.

Identifieur interne : 000C39 ( Main/Curation ); précédent : 000C38; suivant : 000C40

Postural imbalance and falls in PSP correlate with functional pathology of the thalamus.

Auteurs : A. Zwergal [Allemagne] ; C. La Fougère ; S. Lorenzl ; A. Rominger ; G. Xiong ; L. Deutschenbaur ; J. Linn ; S. Krafczyk ; M. Dieterich ; T. Brandt ; M. Strupp ; P. Bartenstein ; K. Jahn

Source :

RBID : pubmed:21613601

Descripteurs français

English descriptors

Abstract

OBJECTIVE

To determine how postural imbalance and falls are related to regional cerebral glucose metabolism (PET) and functional activation of the cerebral postural network (fMRI) in patients with progressive supranuclear palsy (PSP).

METHODS

Sixteen patients with PSP, who had self-monitored their frequency of falls, underwent a standardized clinical assessment, posturographic measurement of balance during modified sensory input, and a resting [¹⁸F]FDG-PET. In addition, patients performed an fMRI paradigm using mental imagery of standing. Results were compared to healthy controls (n = 16).

RESULTS

The frequency of falls/month in patients (range 1-40) correlated with total PSP rating score (r = 0.90). Total sway path in PSP significantly correlated with frequency of falls, especially during modulated sensory input (eyes open: r = 0.62, eyes closed: r = 0.67, eyes open/head extended: r = 0.84, eyes open/foam-padded platform: r = 0.87). Higher sway path values and frequency of falls were associated with decreased regional glucose metabolism (rCGM) in the thalamus (sway path: r = -0.80, falls: r = -0.64) and increased rCGM in the precentral gyrus (sway path: r = 0.79, falls: r = 0.64). Mental imagery of standing during fMRI revealed a reduced activation of the mesencephalic brainstem tegmentum and the thalamus in patients with postural imbalance and falls.

CONCLUSIONS

The new and clinically relevant finding of this study is that imbalance and falls in PSP are closely associated with thalamic dysfunction. Deficits in thalamic postural control get most evident when balance is assessed during modified sensory input. The results are consistent with the hypothesis that reduced thalamic activation via the ascending brainstem projections may cause postural imbalance in PSP.


DOI: 10.1212/WNL.0b013e318223c79d
PubMed: 21613601

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pubmed:21613601

Le document en format XML

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<term>Accidental Falls (MeSH)</term>
<term>Aged (MeSH)</term>
<term>Brain Mapping (MeSH)</term>
<term>Disability Evaluation (MeSH)</term>
<term>Eye (MeSH)</term>
<term>Female (MeSH)</term>
<term>Fluorodeoxyglucose F18 (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Image Processing, Computer-Assisted (MeSH)</term>
<term>Magnetic Resonance Imaging (methods)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Oxygen (blood)</term>
<term>Positron-Emission Tomography (methods)</term>
<term>Postural Balance (physiology)</term>
<term>Rest (MeSH)</term>
<term>Statistics as Topic (MeSH)</term>
<term>Supranuclear Palsy, Progressive (diagnostic imaging)</term>
<term>Supranuclear Palsy, Progressive (pathology)</term>
<term>Supranuclear Palsy, Progressive (physiopathology)</term>
<term>Thalamus (blood supply)</term>
<term>Thalamus (diagnostic imaging)</term>
<term>Thalamus (physiopathology)</term>
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<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte d'âge moyen (MeSH)</term>
<term>Cartographie cérébrale (MeSH)</term>
<term>Chutes accidentelles (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Fluorodésoxyglucose F18 (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Imagerie par résonance magnétique (méthodes)</term>
<term>Mâle (MeSH)</term>
<term>Oeil (MeSH)</term>
<term>Oxygène (sang)</term>
<term>Paralysie supranucléaire progressive (anatomopathologie)</term>
<term>Paralysie supranucléaire progressive (imagerie diagnostique)</term>
<term>Paralysie supranucléaire progressive (physiopathologie)</term>
<term>Repos (MeSH)</term>
<term>Statistiques comme sujet (MeSH)</term>
<term>Sujet âgé (MeSH)</term>
<term>Thalamus (imagerie diagnostique)</term>
<term>Thalamus (physiopathologie)</term>
<term>Thalamus (vascularisation)</term>
<term>Tomographie par émission de positons (méthodes)</term>
<term>Traitement d'image par ordinateur (MeSH)</term>
<term>Équilibre postural (physiologie)</term>
<term>Évaluation de l'invalidité (MeSH)</term>
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<term>Oxygen</term>
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<term>Fluorodeoxyglucose F18</term>
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<term>Paralysie supranucléaire progressive</term>
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<keywords scheme="MESH" qualifier="blood supply" xml:lang="en">
<term>Thalamus</term>
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<keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en">
<term>Supranuclear Palsy, Progressive</term>
<term>Thalamus</term>
</keywords>
<keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr">
<term>Paralysie supranucléaire progressive</term>
<term>Thalamus</term>
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<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Magnetic Resonance Imaging</term>
<term>Positron-Emission Tomography</term>
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<keywords scheme="MESH" qualifier="méthodes" xml:lang="fr">
<term>Imagerie par résonance magnétique</term>
<term>Tomographie par émission de positons</term>
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<term>Supranuclear Palsy, Progressive</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr">
<term>Équilibre postural</term>
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<keywords scheme="MESH" qualifier="physiology" xml:lang="en">
<term>Postural Balance</term>
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<term>Paralysie supranucléaire progressive</term>
<term>Thalamus</term>
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<term>Supranuclear Palsy, Progressive</term>
<term>Thalamus</term>
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<keywords scheme="MESH" qualifier="sang" xml:lang="fr">
<term>Oxygène</term>
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<keywords scheme="MESH" qualifier="vascularisation" xml:lang="fr">
<term>Thalamus</term>
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<keywords scheme="MESH" xml:lang="en">
<term>Accidental Falls</term>
<term>Aged</term>
<term>Brain Mapping</term>
<term>Disability Evaluation</term>
<term>Eye</term>
<term>Female</term>
<term>Humans</term>
<term>Image Processing, Computer-Assisted</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Rest</term>
<term>Statistics as Topic</term>
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<term>Cartographie cérébrale</term>
<term>Chutes accidentelles</term>
<term>Femelle</term>
<term>Fluorodésoxyglucose F18</term>
<term>Humains</term>
<term>Mâle</term>
<term>Oeil</term>
<term>Repos</term>
<term>Statistiques comme sujet</term>
<term>Sujet âgé</term>
<term>Traitement d'image par ordinateur</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>OBJECTIVE</b>
</p>
<p>To determine how postural imbalance and falls are related to regional cerebral glucose metabolism (PET) and functional activation of the cerebral postural network (fMRI) in patients with progressive supranuclear palsy (PSP).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>Sixteen patients with PSP, who had self-monitored their frequency of falls, underwent a standardized clinical assessment, posturographic measurement of balance during modified sensory input, and a resting [¹⁸F]FDG-PET. In addition, patients performed an fMRI paradigm using mental imagery of standing. Results were compared to healthy controls (n = 16).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>The frequency of falls/month in patients (range 1-40) correlated with total PSP rating score (r = 0.90). Total sway path in PSP significantly correlated with frequency of falls, especially during modulated sensory input (eyes open: r = 0.62, eyes closed: r = 0.67, eyes open/head extended: r = 0.84, eyes open/foam-padded platform: r = 0.87). Higher sway path values and frequency of falls were associated with decreased regional glucose metabolism (rCGM) in the thalamus (sway path: r = -0.80, falls: r = -0.64) and increased rCGM in the precentral gyrus (sway path: r = 0.79, falls: r = 0.64). Mental imagery of standing during fMRI revealed a reduced activation of the mesencephalic brainstem tegmentum and the thalamus in patients with postural imbalance and falls.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>The new and clinically relevant finding of this study is that imbalance and falls in PSP are closely associated with thalamic dysfunction. Deficits in thalamic postural control get most evident when balance is assessed during modified sensory input. The results are consistent with the hypothesis that reduced thalamic activation via the ascending brainstem projections may cause postural imbalance in PSP.</p>
</div>
</front>
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<AbstractText Label="METHODS" NlmCategory="METHODS">Sixteen patients with PSP, who had self-monitored their frequency of falls, underwent a standardized clinical assessment, posturographic measurement of balance during modified sensory input, and a resting [¹⁸F]FDG-PET. In addition, patients performed an fMRI paradigm using mental imagery of standing. Results were compared to healthy controls (n = 16).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The frequency of falls/month in patients (range 1-40) correlated with total PSP rating score (r = 0.90). Total sway path in PSP significantly correlated with frequency of falls, especially during modulated sensory input (eyes open: r = 0.62, eyes closed: r = 0.67, eyes open/head extended: r = 0.84, eyes open/foam-padded platform: r = 0.87). Higher sway path values and frequency of falls were associated with decreased regional glucose metabolism (rCGM) in the thalamus (sway path: r = -0.80, falls: r = -0.64) and increased rCGM in the precentral gyrus (sway path: r = 0.79, falls: r = 0.64). Mental imagery of standing during fMRI revealed a reduced activation of the mesencephalic brainstem tegmentum and the thalamus in patients with postural imbalance and falls.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The new and clinically relevant finding of this study is that imbalance and falls in PSP are closely associated with thalamic dysfunction. Deficits in thalamic postural control get most evident when balance is assessed during modified sensory input. The results are consistent with the hypothesis that reduced thalamic activation via the ascending brainstem projections may cause postural imbalance in PSP.</AbstractText>
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<DescriptorName UI="D001931" MajorTopicYN="N">Brain Mapping</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D004185" MajorTopicYN="N">Disability Evaluation</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D005123" MajorTopicYN="N">Eye</DescriptorName>
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<DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
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<MeshHeading>
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