Does pallidal neuromodulation influence cognitive decline in Huntington’s disease?
Objective Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder associated with motor, psychiatric and cognitive deterioration over time. To date, Continuous Electrical Neuromodulation (CEN) of the globus pallidus internus (GPi) has been reported to improve chorea but little...
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Veröffentlicht in: | Journal of neurology 2021-02, Vol.268 (2), p.613-622 |
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creator | Sanrey, Emily Macioce, Valérie Gonzalez, Victoria Cif, Laura Cyprien, Fabienne Chan Seng, Emilie Coubes, Philippe Poulen, Gaetan |
description | Objective
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder associated with motor, psychiatric and cognitive deterioration over time. To date, Continuous Electrical Neuromodulation (CEN) of the globus pallidus internus (GPi) has been reported to improve chorea but little is known about cognitive progression in these patients. We propose to examine CEN impact on expected cognitive decline throughout long-term neuropsychological assessment of a cohort of HD patients.
Method
13 consecutive HD patients underwent GPi neuromodulation between January 2008 and February 2019. Over a 5-year follow-up period, they received systematic pre- and post-operative assessment according to the existing protocol in our unit. The main outcome measure was the total score obtained on the Mattis Dementia Rating Scale (MDRS) as an indicator of global cognitive function.
Results
Chorea decreased in all patients postoperatively with a mean improvement of 56% despite disease progression over time, according to previous studies. Moreover we found that the global cognitive profile of HD patients treated with CEN was stable during the first 3 years of treatment.
Conclusion
We report an unexpected positive influence of GPi continuous electrical neuromodulation on the progression of global cognitive functioning in operated HD patients. This is the most important group of patients treated with this method to our knowledge whatever the sample size remains small. This result provides promising evidence of GPi-CEN efficacy not only in reducing chorea, but also in delaying cognitive decline in HD patients operated at an early stage of the disease. |
doi_str_mv | 10.1007/s00415-020-10206-w |
format | Article |
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Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder associated with motor, psychiatric and cognitive deterioration over time. To date, Continuous Electrical Neuromodulation (CEN) of the globus pallidus internus (GPi) has been reported to improve chorea but little is known about cognitive progression in these patients. We propose to examine CEN impact on expected cognitive decline throughout long-term neuropsychological assessment of a cohort of HD patients.
Method
13 consecutive HD patients underwent GPi neuromodulation between January 2008 and February 2019. Over a 5-year follow-up period, they received systematic pre- and post-operative assessment according to the existing protocol in our unit. The main outcome measure was the total score obtained on the Mattis Dementia Rating Scale (MDRS) as an indicator of global cognitive function.
Results
Chorea decreased in all patients postoperatively with a mean improvement of 56% despite disease progression over time, according to previous studies. Moreover we found that the global cognitive profile of HD patients treated with CEN was stable during the first 3 years of treatment.
Conclusion
We report an unexpected positive influence of GPi continuous electrical neuromodulation on the progression of global cognitive functioning in operated HD patients. This is the most important group of patients treated with this method to our knowledge whatever the sample size remains small. This result provides promising evidence of GPi-CEN efficacy not only in reducing chorea, but also in delaying cognitive decline in HD patients operated at an early stage of the disease.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-020-10206-w</identifier><identifier>PMID: 32886253</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Chorea ; Cognitive ability ; Cognitive Dysfunction ; Deep Brain Stimulation ; Dementia ; Dementia disorders ; Disease ; Globus Pallidus ; Hereditary diseases ; Human health and pathology ; Humans ; Huntington Disease ; Huntington's disease ; Huntingtons disease ; Life Sciences ; Medicine ; Medicine & Public Health ; Neurodegenerative diseases ; Neurology ; Neuromodulation ; Neurons and Cognition ; Neuropsychology ; Neuroradiology ; Neurosciences ; Original Communication ; Patients ; Surgery</subject><ispartof>Journal of neurology, 2021-02, Vol.268 (2), p.613-622</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-fceb5a5979981ddaacdec7ac627878eee5a9507428cea05fad0c56109a8674e23</citedby><cites>FETCH-LOGICAL-c409t-fceb5a5979981ddaacdec7ac627878eee5a9507428cea05fad0c56109a8674e23</cites><orcidid>0000-0001-7942-5279 ; 0000-0003-4920-4234 ; 0000-0002-1323-301X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00415-020-10206-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00415-020-10206-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32886253$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.umontpellier.fr/hal-03340973$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Sanrey, Emily</creatorcontrib><creatorcontrib>Macioce, Valérie</creatorcontrib><creatorcontrib>Gonzalez, Victoria</creatorcontrib><creatorcontrib>Cif, Laura</creatorcontrib><creatorcontrib>Cyprien, Fabienne</creatorcontrib><creatorcontrib>Chan Seng, Emilie</creatorcontrib><creatorcontrib>Coubes, Philippe</creatorcontrib><creatorcontrib>Poulen, Gaetan</creatorcontrib><title>Does pallidal neuromodulation influence cognitive decline in Huntington’s disease?</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Objective
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder associated with motor, psychiatric and cognitive deterioration over time. To date, Continuous Electrical Neuromodulation (CEN) of the globus pallidus internus (GPi) has been reported to improve chorea but little is known about cognitive progression in these patients. We propose to examine CEN impact on expected cognitive decline throughout long-term neuropsychological assessment of a cohort of HD patients.
Method
13 consecutive HD patients underwent GPi neuromodulation between January 2008 and February 2019. Over a 5-year follow-up period, they received systematic pre- and post-operative assessment according to the existing protocol in our unit. The main outcome measure was the total score obtained on the Mattis Dementia Rating Scale (MDRS) as an indicator of global cognitive function.
Results
Chorea decreased in all patients postoperatively with a mean improvement of 56% despite disease progression over time, according to previous studies. Moreover we found that the global cognitive profile of HD patients treated with CEN was stable during the first 3 years of treatment.
Conclusion
We report an unexpected positive influence of GPi continuous electrical neuromodulation on the progression of global cognitive functioning in operated HD patients. This is the most important group of patients treated with this method to our knowledge whatever the sample size remains small. This result provides promising evidence of GPi-CEN efficacy not only in reducing chorea, but also in delaying cognitive decline in HD patients operated at an early stage of the disease.</description><subject>Chorea</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction</subject><subject>Deep Brain Stimulation</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Disease</subject><subject>Globus Pallidus</subject><subject>Hereditary diseases</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Huntington Disease</subject><subject>Huntington's disease</subject><subject>Huntingtons disease</subject><subject>Life Sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neurodegenerative diseases</subject><subject>Neurology</subject><subject>Neuromodulation</subject><subject>Neurons and Cognition</subject><subject>Neuropsychology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Original Communication</subject><subject>Patients</subject><subject>Surgery</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc9O3DAQxq2qqCy0L9ADitRLewiM_8XOqUK0sEgr9QJnyziTrZHXXuIE1Ftfo6_Hk9TbUJB66MUj-fvNN_Z8hLyncEwB1EkGEFTWwKCm5Wjqh1dkQQVnNRWyfU0WwAXUkkuxTw5yvgUAXYQ3ZJ8zrRsm-YJcfUmYq60NwXc2VBGnIW1SNwU7-hQrH_swYXRYubSOfvT3WHXogo9YtGo5xdHH9Zji489fuep8Rpvx81uy19uQ8d1TPSTX51-vzpb16tvF5dnpqnYC2rHuHd5IK1vVtpp2nbWuWCvrGqa00ogobStBCaYdWpC97cDJhkJrdaMEMn5IPs2-320w28Fv7PDDJOvN8nRldnfAywZaxe9pYT_O7HZIdxPm0Wx8dhiCjZimbJgQIBRItUM__IPepmmI5SeF0loprTkvFJspN6ScB-yfX0DB7PIxcz6mRGP-5GMeStPRk_V0s8HuueVvIAXgM5CLFNc4vMz-j-1vKZOcUg</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Sanrey, Emily</creator><creator>Macioce, Valérie</creator><creator>Gonzalez, Victoria</creator><creator>Cif, Laura</creator><creator>Cyprien, Fabienne</creator><creator>Chan Seng, Emilie</creator><creator>Coubes, Philippe</creator><creator>Poulen, Gaetan</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><general>Springer Verlag</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0001-7942-5279</orcidid><orcidid>https://orcid.org/0000-0003-4920-4234</orcidid><orcidid>https://orcid.org/0000-0002-1323-301X</orcidid></search><sort><creationdate>20210201</creationdate><title>Does pallidal neuromodulation influence cognitive decline in Huntington’s disease?</title><author>Sanrey, Emily ; Macioce, Valérie ; Gonzalez, Victoria ; Cif, Laura ; Cyprien, Fabienne ; Chan Seng, Emilie ; Coubes, Philippe ; Poulen, Gaetan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-fceb5a5979981ddaacdec7ac627878eee5a9507428cea05fad0c56109a8674e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Chorea</topic><topic>Cognitive ability</topic><topic>Cognitive Dysfunction</topic><topic>Deep Brain Stimulation</topic><topic>Dementia</topic><topic>Dementia disorders</topic><topic>Disease</topic><topic>Globus Pallidus</topic><topic>Hereditary diseases</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Huntington Disease</topic><topic>Huntington's disease</topic><topic>Huntingtons disease</topic><topic>Life Sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neurodegenerative diseases</topic><topic>Neurology</topic><topic>Neuromodulation</topic><topic>Neurons and Cognition</topic><topic>Neuropsychology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Original Communication</topic><topic>Patients</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sanrey, Emily</creatorcontrib><creatorcontrib>Macioce, Valérie</creatorcontrib><creatorcontrib>Gonzalez, Victoria</creatorcontrib><creatorcontrib>Cif, Laura</creatorcontrib><creatorcontrib>Cyprien, Fabienne</creatorcontrib><creatorcontrib>Chan Seng, Emilie</creatorcontrib><creatorcontrib>Coubes, Philippe</creatorcontrib><creatorcontrib>Poulen, Gaetan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sanrey, Emily</au><au>Macioce, Valérie</au><au>Gonzalez, Victoria</au><au>Cif, Laura</au><au>Cyprien, Fabienne</au><au>Chan Seng, Emilie</au><au>Coubes, Philippe</au><au>Poulen, Gaetan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does pallidal neuromodulation influence cognitive decline in Huntington’s disease?</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>268</volume><issue>2</issue><spage>613</spage><epage>622</epage><pages>613-622</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><abstract>Objective
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder associated with motor, psychiatric and cognitive deterioration over time. To date, Continuous Electrical Neuromodulation (CEN) of the globus pallidus internus (GPi) has been reported to improve chorea but little is known about cognitive progression in these patients. We propose to examine CEN impact on expected cognitive decline throughout long-term neuropsychological assessment of a cohort of HD patients.
Method
13 consecutive HD patients underwent GPi neuromodulation between January 2008 and February 2019. Over a 5-year follow-up period, they received systematic pre- and post-operative assessment according to the existing protocol in our unit. The main outcome measure was the total score obtained on the Mattis Dementia Rating Scale (MDRS) as an indicator of global cognitive function.
Results
Chorea decreased in all patients postoperatively with a mean improvement of 56% despite disease progression over time, according to previous studies. Moreover we found that the global cognitive profile of HD patients treated with CEN was stable during the first 3 years of treatment.
Conclusion
We report an unexpected positive influence of GPi continuous electrical neuromodulation on the progression of global cognitive functioning in operated HD patients. This is the most important group of patients treated with this method to our knowledge whatever the sample size remains small. This result provides promising evidence of GPi-CEN efficacy not only in reducing chorea, but also in delaying cognitive decline in HD patients operated at an early stage of the disease.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32886253</pmid><doi>10.1007/s00415-020-10206-w</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-7942-5279</orcidid><orcidid>https://orcid.org/0000-0003-4920-4234</orcidid><orcidid>https://orcid.org/0000-0002-1323-301X</orcidid></addata></record> |
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subjects | Chorea Cognitive ability Cognitive Dysfunction Deep Brain Stimulation Dementia Dementia disorders Disease Globus Pallidus Hereditary diseases Human health and pathology Humans Huntington Disease Huntington's disease Huntingtons disease Life Sciences Medicine Medicine & Public Health Neurodegenerative diseases Neurology Neuromodulation Neurons and Cognition Neuropsychology Neuroradiology Neurosciences Original Communication Patients Surgery |
title | Does pallidal neuromodulation influence cognitive decline in Huntington’s disease? |
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