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Functional involvement of central cholinergic circuits and visual hallucinations in Parkinson's disease
Visual hallucinations (VHs) represent a frequent and disturbing complication of Parkinson's disease. Evidence suggests that VH can be related to central cholinergic dysfunction. Short-latency afferent inhibition (SAI) technique gives the opportunity to test an inhibitory cholinergic circuit in...
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Published in: | Brain (London, England : 1878) England : 1878), 2009-09, Vol.132 (9), p.2350-2355 |
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creator | Manganelli, Fiore Vitale, Carmine Santangelo, Gabriella Pisciotta, Chiara Iodice, Rosa Cozzolino, Autilia Dubbioso, Raffaele Picillo, Marina Barone, Paolo Santoro, Lucio |
description | Visual hallucinations (VHs) represent a frequent and disturbing complication of Parkinson's disease. Evidence suggests that VH can be related to central cholinergic dysfunction. Short-latency afferent inhibition (SAI) technique gives the opportunity to test an inhibitory cholinergic circuit in the human cerebral motor cortex. This inhibition of motor-evoked potentials can be observed when transcranial magnetic stimulation is delivered with a delay ranging from 2 to 8 ms, after a peripheral nerve afferent input has reached the somatosensory cortex. We applied SAI technique in 10 non-demented patients with Parkinson's disease with VHs, in 12 non-demented patients with Parkinson's disease without VHs (NVH-pts) and in 11 age-matched normal controls. All patients with Parkinson's disease underwent a battery of neuropsychological tests to assess frontal and visuospatial functions, memory and attention. SAI was significantly reduced in patients with VHs compared with controls and patients without VHs. Neuropsychological examination showed a mild cognitive impairment in 16 out of 22 patients with Parkinson's disease. In addition, we found that in our patients with VHs, performance of some tasks evaluating visuospatial functions and attentional/frontal lobe functions was significantly more impaired than in patients without VHs. SAI abnormalities, presence of VH and neuropsychological results strongly support the hypothesis of cholinergic dysfunction in some patients with Parkinson's disease, who will probably develop a dementia. A follow-up study of our patients is required to verify whether SAI abnormalities can predict a future severe cognitive decline. Moreover, SAI can also be very useful to follow-up the efficacy of anti-cholinesterase therapies. |
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Evidence suggests that VH can be related to central cholinergic dysfunction. Short-latency afferent inhibition (SAI) technique gives the opportunity to test an inhibitory cholinergic circuit in the human cerebral motor cortex. This inhibition of motor-evoked potentials can be observed when transcranial magnetic stimulation is delivered with a delay ranging from 2 to 8 ms, after a peripheral nerve afferent input has reached the somatosensory cortex. We applied SAI technique in 10 non-demented patients with Parkinson's disease with VHs, in 12 non-demented patients with Parkinson's disease without VHs (NVH-pts) and in 11 age-matched normal controls. All patients with Parkinson's disease underwent a battery of neuropsychological tests to assess frontal and visuospatial functions, memory and attention. SAI was significantly reduced in patients with VHs compared with controls and patients without VHs. Neuropsychological examination showed a mild cognitive impairment in 16 out of 22 patients with Parkinson's disease. In addition, we found that in our patients with VHs, performance of some tasks evaluating visuospatial functions and attentional/frontal lobe functions was significantly more impaired than in patients without VHs. SAI abnormalities, presence of VH and neuropsychological results strongly support the hypothesis of cholinergic dysfunction in some patients with Parkinson's disease, who will probably develop a dementia. A follow-up study of our patients is required to verify whether SAI abnormalities can predict a future severe cognitive decline. Moreover, SAI can also be very useful to follow-up the efficacy of anti-cholinesterase therapies.</description><identifier>ISSN: 0006-8950</identifier><identifier>EISSN: 1460-2156</identifier><identifier>DOI: 10.1093/brain/awp166</identifier><identifier>PMID: 19584099</identifier><identifier>CODEN: BRAIAK</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Aged ; Aged, 80 and over ; Biological and medical sciences ; Cholinergic Fibers - physiology ; Cognition Disorders - etiology ; Cognition Disorders - physiopathology ; cognitive deficits ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Evoked Potentials, Motor - physiology ; Female ; Hallucinations - etiology ; Hallucinations - physiopathology ; Humans ; Male ; Medical sciences ; Middle Aged ; Motor Cortex - physiopathology ; Neural Inhibition - physiology ; Neurology ; Neuropsychological Tests ; Original ; Parkinson Disease - physiopathology ; Parkinson Disease - psychology ; Parkinson's disease ; Reaction Time - physiology ; short-latency afferent inhibition ; TMS ; Transcranial Magnetic Stimulation - methods ; visual hallucinations</subject><ispartof>Brain (London, England : 1878), 2009-09, Vol.132 (9), p.2350-2355</ispartof><rights>The Author (2009). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2009</rights><rights>2009 INIST-CNRS</rights><rights>The Author (2009). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c607t-7ad1920035053a727187f855166aa3af52d1154d15b95abcf9036255598589513</citedby><cites>FETCH-LOGICAL-c607t-7ad1920035053a727187f855166aa3af52d1154d15b95abcf9036255598589513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21895818$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19584099$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Manganelli, Fiore</creatorcontrib><creatorcontrib>Vitale, Carmine</creatorcontrib><creatorcontrib>Santangelo, Gabriella</creatorcontrib><creatorcontrib>Pisciotta, Chiara</creatorcontrib><creatorcontrib>Iodice, Rosa</creatorcontrib><creatorcontrib>Cozzolino, Autilia</creatorcontrib><creatorcontrib>Dubbioso, Raffaele</creatorcontrib><creatorcontrib>Picillo, Marina</creatorcontrib><creatorcontrib>Barone, Paolo</creatorcontrib><creatorcontrib>Santoro, Lucio</creatorcontrib><title>Functional involvement of central cholinergic circuits and visual hallucinations in Parkinson's disease</title><title>Brain (London, England : 1878)</title><addtitle>Brain</addtitle><description>Visual hallucinations (VHs) represent a frequent and disturbing complication of Parkinson's disease. Evidence suggests that VH can be related to central cholinergic dysfunction. Short-latency afferent inhibition (SAI) technique gives the opportunity to test an inhibitory cholinergic circuit in the human cerebral motor cortex. This inhibition of motor-evoked potentials can be observed when transcranial magnetic stimulation is delivered with a delay ranging from 2 to 8 ms, after a peripheral nerve afferent input has reached the somatosensory cortex. We applied SAI technique in 10 non-demented patients with Parkinson's disease with VHs, in 12 non-demented patients with Parkinson's disease without VHs (NVH-pts) and in 11 age-matched normal controls. All patients with Parkinson's disease underwent a battery of neuropsychological tests to assess frontal and visuospatial functions, memory and attention. SAI was significantly reduced in patients with VHs compared with controls and patients without VHs. Neuropsychological examination showed a mild cognitive impairment in 16 out of 22 patients with Parkinson's disease. In addition, we found that in our patients with VHs, performance of some tasks evaluating visuospatial functions and attentional/frontal lobe functions was significantly more impaired than in patients without VHs. SAI abnormalities, presence of VH and neuropsychological results strongly support the hypothesis of cholinergic dysfunction in some patients with Parkinson's disease, who will probably develop a dementia. A follow-up study of our patients is required to verify whether SAI abnormalities can predict a future severe cognitive decline. 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Prion diseases</subject><subject>Evoked Potentials, Motor - physiology</subject><subject>Female</subject><subject>Hallucinations - etiology</subject><subject>Hallucinations - physiopathology</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Motor Cortex - physiopathology</subject><subject>Neural Inhibition - physiology</subject><subject>Neurology</subject><subject>Neuropsychological Tests</subject><subject>Original</subject><subject>Parkinson Disease - physiopathology</subject><subject>Parkinson Disease - psychology</subject><subject>Parkinson's disease</subject><subject>Reaction Time - physiology</subject><subject>short-latency afferent inhibition</subject><subject>TMS</subject><subject>Transcranial Magnetic Stimulation - methods</subject><subject>visual hallucinations</subject><issn>0006-8950</issn><issn>1460-2156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkc1vEzEQxS0EoqFw44xWSNALS_2x3rUvSCiiDVIlWlQkxMWaeL2Jy8ZOPbsB_nscEqXAAU4jeX564_ceIU8Zfc2oFqfzBD6cwrc1q-t7ZMKqmpacyfo-mVBK61JpSY_II8QbSlkleP2QHDEtVUW1npDF2Rjs4GOAvvBhE_uNW7kwFLErbJ4pP9tl7H1waeFtYX2yox-wgNAWG49j3i-h70frA2xlMKsUl5C--oAxnGDRenSA7jF50EGP7sl-HpNPZ--up7Py4sP5--nbi9LWtBnKBlqmOaVCUimg4Q1TTaekzN4ABHSSt4zJqmVyriXMbaepqLmUUiuZjTJxTN7sdNfjfOXavQezTn4F6YeJ4M2fm-CXZhE3hqt8VYkscLIXSPF2dDiYlUfr-h6CiyOaRlSU5fBUJl_-k-SZoZrRDD7_C7yJY8qJo8lFVGzrLkOvdpBNETG57vBnRs22aPOraLMrOuPPfvd5B--bzcCLPQBooe8SBOvxwHGW41JM3fmN4_p_J8sd6XFw3w9s7trUjWikmX3-Yq6u-fnl7OPUXImfYnTQBQ</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>Manganelli, Fiore</creator><creator>Vitale, Carmine</creator><creator>Santangelo, Gabriella</creator><creator>Pisciotta, Chiara</creator><creator>Iodice, Rosa</creator><creator>Cozzolino, Autilia</creator><creator>Dubbioso, Raffaele</creator><creator>Picillo, Marina</creator><creator>Barone, Paolo</creator><creator>Santoro, Lucio</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090901</creationdate><title>Functional involvement of central cholinergic circuits and visual hallucinations in Parkinson's disease</title><author>Manganelli, Fiore ; Vitale, Carmine ; Santangelo, Gabriella ; Pisciotta, Chiara ; Iodice, Rosa ; Cozzolino, Autilia ; Dubbioso, Raffaele ; Picillo, Marina ; Barone, Paolo ; Santoro, Lucio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c607t-7ad1920035053a727187f855166aa3af52d1154d15b95abcf9036255598589513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Cholinergic Fibers - physiology</topic><topic>Cognition Disorders - etiology</topic><topic>Cognition Disorders - physiopathology</topic><topic>cognitive deficits</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Evoked Potentials, Motor - physiology</topic><topic>Female</topic><topic>Hallucinations - etiology</topic><topic>Hallucinations - physiopathology</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Motor Cortex - physiopathology</topic><topic>Neural Inhibition - physiology</topic><topic>Neurology</topic><topic>Neuropsychological Tests</topic><topic>Original</topic><topic>Parkinson Disease - physiopathology</topic><topic>Parkinson Disease - psychology</topic><topic>Parkinson's disease</topic><topic>Reaction Time - physiology</topic><topic>short-latency afferent inhibition</topic><topic>TMS</topic><topic>Transcranial Magnetic Stimulation - methods</topic><topic>visual hallucinations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Manganelli, Fiore</creatorcontrib><creatorcontrib>Vitale, Carmine</creatorcontrib><creatorcontrib>Santangelo, Gabriella</creatorcontrib><creatorcontrib>Pisciotta, Chiara</creatorcontrib><creatorcontrib>Iodice, Rosa</creatorcontrib><creatorcontrib>Cozzolino, Autilia</creatorcontrib><creatorcontrib>Dubbioso, Raffaele</creatorcontrib><creatorcontrib>Picillo, Marina</creatorcontrib><creatorcontrib>Barone, Paolo</creatorcontrib><creatorcontrib>Santoro, Lucio</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Brain (London, England : 1878)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Manganelli, Fiore</au><au>Vitale, Carmine</au><au>Santangelo, Gabriella</au><au>Pisciotta, Chiara</au><au>Iodice, Rosa</au><au>Cozzolino, Autilia</au><au>Dubbioso, Raffaele</au><au>Picillo, Marina</au><au>Barone, Paolo</au><au>Santoro, Lucio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional involvement of central cholinergic circuits and visual hallucinations in Parkinson's disease</atitle><jtitle>Brain (London, England : 1878)</jtitle><addtitle>Brain</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>132</volume><issue>9</issue><spage>2350</spage><epage>2355</epage><pages>2350-2355</pages><issn>0006-8950</issn><eissn>1460-2156</eissn><coden>BRAIAK</coden><abstract>Visual hallucinations (VHs) represent a frequent and disturbing complication of Parkinson's disease. Evidence suggests that VH can be related to central cholinergic dysfunction. Short-latency afferent inhibition (SAI) technique gives the opportunity to test an inhibitory cholinergic circuit in the human cerebral motor cortex. This inhibition of motor-evoked potentials can be observed when transcranial magnetic stimulation is delivered with a delay ranging from 2 to 8 ms, after a peripheral nerve afferent input has reached the somatosensory cortex. We applied SAI technique in 10 non-demented patients with Parkinson's disease with VHs, in 12 non-demented patients with Parkinson's disease without VHs (NVH-pts) and in 11 age-matched normal controls. All patients with Parkinson's disease underwent a battery of neuropsychological tests to assess frontal and visuospatial functions, memory and attention. SAI was significantly reduced in patients with VHs compared with controls and patients without VHs. Neuropsychological examination showed a mild cognitive impairment in 16 out of 22 patients with Parkinson's disease. In addition, we found that in our patients with VHs, performance of some tasks evaluating visuospatial functions and attentional/frontal lobe functions was significantly more impaired than in patients without VHs. SAI abnormalities, presence of VH and neuropsychological results strongly support the hypothesis of cholinergic dysfunction in some patients with Parkinson's disease, who will probably develop a dementia. A follow-up study of our patients is required to verify whether SAI abnormalities can predict a future severe cognitive decline. Moreover, SAI can also be very useful to follow-up the efficacy of anti-cholinesterase therapies.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>19584099</pmid><doi>10.1093/brain/awp166</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Biological and medical sciences Cholinergic Fibers - physiology Cognition Disorders - etiology Cognition Disorders - physiopathology cognitive deficits Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Evoked Potentials, Motor - physiology Female Hallucinations - etiology Hallucinations - physiopathology Humans Male Medical sciences Middle Aged Motor Cortex - physiopathology Neural Inhibition - physiology Neurology Neuropsychological Tests Original Parkinson Disease - physiopathology Parkinson Disease - psychology Parkinson's disease Reaction Time - physiology short-latency afferent inhibition TMS Transcranial Magnetic Stimulation - methods visual hallucinations |
title | Functional involvement of central cholinergic circuits and visual hallucinations in Parkinson's disease |
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