Movement Disorders (revue)

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123I‐metaiodobenzylguanidine scintigraphy in Parkinson's disease and related disorders

Identifieur interne : 000A47 ( Istex/Corpus ); précédent : 000A46; suivant : 000A48

123I‐metaiodobenzylguanidine scintigraphy in Parkinson's disease and related disorders

Auteurs : Olivier Rascol ; Ludwig Schelosky

Source :

RBID : ISTEX:F0E4F24A5977047882DC9362028C31CB5E425B21

English descriptors

Abstract

Autonomic dysfunction is common in Lewy body disorders (Parkinson's disease, Dementia with Lewy Bodies, Pure Autonomic Failure, and REM sleep disorder). The loss of post‐ganglionic myocardial sympathetic nerve fibers is a prominent feature of autonomic dysfunction in such disorders. 123I‐metaiodobenzylguanidine (MIBG) scintigraphy that visualizes catecholaminergic terminals in vivo is a biomarker used to detect cardiac sympathetic degeneration. Abnormal MIBG uptake has been consistently reported in Lewy body disorders. Some studies agree in the notion that increasing bradykinesia is related with an incremental cardiac sympathetic denervation, whereas tremor is not closely linked to cardiac denervation. “Atypical” parkinsonian syndromes, including Multiple System Atrophy, Progressive Supranuclear Palsy, and others, show modest reductions of cardial MIBG uptake. MIBG scintigraphy is moderately sensitive and specific in differentiating Parkinson's disease from such syndromes. Conversely, its sensitivity and specificity might be better in cognitively impaired patients, helping differential diagnosis between Dementia with Lewy Bodies, and Alzheimer disease. Confounding factors (comorbidities, comedications) should be carefully controlled before analyzing MIBG scintigraphy. © 2009 Movement Disorder Society

Url:
DOI: 10.1002/mds.22499

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ISTEX:F0E4F24A5977047882DC9362028C31CB5E425B21

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I‐metaiodobenzylguanidine scintigraphy in Parkinson's disease and related disorders
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<abstract lang="en">Autonomic dysfunction is common in Lewy body disorders (Parkinson's disease, Dementia with Lewy Bodies, Pure Autonomic Failure, and REM sleep disorder). The loss of post‐ganglionic myocardial sympathetic nerve fibers is a prominent feature of autonomic dysfunction in such disorders. 123I‐metaiodobenzylguanidine (MIBG) scintigraphy that visualizes catecholaminergic terminals in vivo is a biomarker used to detect cardiac sympathetic degeneration. Abnormal MIBG uptake has been consistently reported in Lewy body disorders. Some studies agree in the notion that increasing bradykinesia is related with an incremental cardiac sympathetic denervation, whereas tremor is not closely linked to cardiac denervation. “Atypical” parkinsonian syndromes, including Multiple System Atrophy, Progressive Supranuclear Palsy, and others, show modest reductions of cardial MIBG uptake. MIBG scintigraphy is moderately sensitive and specific in differentiating Parkinson's disease from such syndromes. Conversely, its sensitivity and specificity might be better in cognitively impaired patients, helping differential diagnosis between Dementia with Lewy Bodies, and Alzheimer disease. Confounding factors (comorbidities, comedications) should be carefully controlled before analyzing MIBG scintigraphy. © 2009 Movement Disorder Society</abstract>
<note type="content">*Potential Conflict of Interest: L.S. has received honoraria from Boehringer Ingelheim in 2008.</note>
<subject lang="en">
<genre>Keywords</genre>
<topic>MIBG scintigraphy</topic>
<topic>autonomic nervous system</topic>
<topic>cardiac sympathetic innervation</topic>
<topic>differential diagnosis</topic>
<topic>Parkinson's disease</topic>
<topic>MSA</topic>
</subject>
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<title>Movement Disorders</title>
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<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
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<subject>
<genre>article category</genre>
<topic>Research Article</topic>
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<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
<part>
<date>2009</date>
<detail type="volume">
<caption>vol.</caption>
<number>24</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>S2</number>
</detail>
<extent unit="pages">
<start>S732</start>
<end>S741</end>
<total>10</total>
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<identifier type="istex">F0E4F24A5977047882DC9362028C31CB5E425B21</identifier>
<identifier type="DOI">10.1002/mds.22499</identifier>
<identifier type="ArticleID">MDS22499</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2009 Movement Disorder Society</accessCondition>
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