Movement Disorders (revue)

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PET study of brain acetylcholinesterase in cerebellar degenerative disorders

Identifieur interne : 002719 ( Main/Exploration ); précédent : 002718; suivant : 002720

PET study of brain acetylcholinesterase in cerebellar degenerative disorders

Auteurs : Shigeki Hirano [Japon] ; Hitoshi Shinotoh [Japon] ; Kimihito Arai [Japon] ; Akiyo Aotsuka [Japon] ; Fumihiko Yasuno [Japon] ; Noriko Tanaka [Japon] ; Tsuneyoshi Ota [Japon] ; Koichi Sato [Japon] ; Kiyoshi Fukushi [Japon] ; Shuji Tanada [Japon] ; Takamichi Hattori [Japon] ; Toshiaki Irie [Japon]

Source :

RBID : ISTEX:16B3D727105BC3F28F6FBF8B40F670E455699ECC

Descripteurs français

English descriptors

Abstract

To elucidate characteristic changes of brain acetylcholinesterase (AChE) in cerebellar degenerative disorders. Eight patients with the cerebellar variant of multiple system atrophy (MSA‐C), 7 patients with spinocerebellar ataxia type‐3 (SCA‐3), 3 patients with SCA‐6, and 13 healthy age‐matched volunteers participated in this study. Brain AChE activity was measured by [11C] N‐methylpiperidin‐4‐yl propionate PET in all subjects. Brain AChE activities were significantly decreased in the thalamus (−27%) and the posterior lobe of cerebellar cortex (−36%) in patients with MSA‐C and in the thalamus (−23%) in patients with SCA‐3 compared with healthy controls (P < 0.01). Thalamic AChE activities of SCA‐3 patients were negatively correlated with the unified Parkinson's disease rating scale motor subscore (P < 0.001). AChE activities were not significantly altered in the cerebral cortex in any disease group. Reduction of AChE activities in the thalamus and cerebellum in MSA and in the thalamus in SCA‐3 suggest that cholinergic modulating drugs may have a role in the treatment of ataxia and other symptoms in these disorders. © 2008 Movement Disorder Society

Url:
DOI: 10.1002/mds.22056


Affiliations:


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Le document en format XML

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<term>Acetylcholine</term>
<term>Acetylcholinesterase</term>
<term>Acetylcholinesterase (metabolism)</term>
<term>Adult</term>
<term>Aged</term>
<term>Brain (radionuclide imaging)</term>
<term>Carbon Radioisotopes (diagnostic use)</term>
<term>Cerebellar Cortex (radionuclide imaging)</term>
<term>Cerebellum</term>
<term>Cerebral Cortex (radionuclide imaging)</term>
<term>Emission tomography</term>
<term>Encephalon</term>
<term>Female</term>
<term>Humans</term>
<term>Image Processing, Computer-Assisted</term>
<term>Machado-Joseph Disease (radionuclide imaging)</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Multiple System Atrophy (radionuclide imaging)</term>
<term>Multiple system atrophy</term>
<term>Nervous system diseases</term>
<term>Neurologic Examination</term>
<term>Piperidines (diagnostic use)</term>
<term>Positron emission tomography</term>
<term>Positron-Emission Tomography</term>
<term>Propionates (diagnostic use)</term>
<term>Spinocerebellar Ataxias (radionuclide imaging)</term>
<term>Spinocerebellar Degenerations (radionuclide imaging)</term>
<term>Spinocerebellar ataxia</term>
<term>Thalamus</term>
<term>Thalamus (radionuclide imaging)</term>
<term>acetylcholine</term>
<term>multiple system atrophy</term>
<term>positron emission tomography</term>
<term>spinocerebellar ataxia</term>
<term>thalamus</term>
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<term>Piperidines</term>
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<term>Acetylcholinesterase</term>
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<term>Brain</term>
<term>Cerebellar Cortex</term>
<term>Cerebral Cortex</term>
<term>Machado-Joseph Disease</term>
<term>Multiple System Atrophy</term>
<term>Spinocerebellar Ataxias</term>
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<term>Magnetic Resonance Imaging</term>
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<term>Middle Aged</term>
<term>Neurologic Examination</term>
<term>Positron-Emission Tomography</term>
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<term>Acetylcholinesterase</term>
<term>Acétylcholine</term>
<term>Ataxie spinocérébelleuse</term>
<term>Atrophie multisystématisée</term>
<term>Cervelet</term>
<term>Encéphale</term>
<term>Pathologie du système nerveux</term>
<term>Thalamus</term>
<term>Tomographie par émission de positons</term>
<term>Tomoscintigraphie</term>
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<div type="abstract" xml:lang="en">To elucidate characteristic changes of brain acetylcholinesterase (AChE) in cerebellar degenerative disorders. Eight patients with the cerebellar variant of multiple system atrophy (MSA‐C), 7 patients with spinocerebellar ataxia type‐3 (SCA‐3), 3 patients with SCA‐6, and 13 healthy age‐matched volunteers participated in this study. Brain AChE activity was measured by [11C] N‐methylpiperidin‐4‐yl propionate PET in all subjects. Brain AChE activities were significantly decreased in the thalamus (−27%) and the posterior lobe of cerebellar cortex (−36%) in patients with MSA‐C and in the thalamus (−23%) in patients with SCA‐3 compared with healthy controls (P < 0.01). Thalamic AChE activities of SCA‐3 patients were negatively correlated with the unified Parkinson's disease rating scale motor subscore (P < 0.001). AChE activities were not significantly altered in the cerebral cortex in any disease group. Reduction of AChE activities in the thalamus and cerebellum in MSA and in the thalamus in SCA‐3 suggest that cholinergic modulating drugs may have a role in the treatment of ataxia and other symptoms in these disorders. © 2008 Movement Disorder Society</div>
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