Altered functional connectivity in lesional peduncular hallucinosis with REM sleep behavior disorder.
Identifieur interne : 000325 ( PubMed/Checkpoint ); précédent : 000324; suivant : 000326Altered functional connectivity in lesional peduncular hallucinosis with REM sleep behavior disorder.
Auteurs : Maiya R. Geddes [États-Unis] ; Yanmei Tie [États-Unis] ; John D E. Gabrieli [États-Unis] ; Scott M. Mcginnis [États-Unis] ; Alexandra J. Golby [États-Unis] ; Susan Whitfield-Gabrieli [États-Unis]Source :
- Cortex; a journal devoted to the study of the nervous system and behavior [ 1973-8102 ] ; 2016.
English descriptors
- KwdEn :
- Aged, Brain Ischemia (physiopathology), Geniculate Bodies (physiopathology), Hallucinations (physiopathology), Humans, Magnetic Resonance Imaging, Male, Nerve Net (physiopathology), Polysomnography, Pons (physiopathology), REM Sleep Behavior Disorder (physiopathology), Stroke (physiopathology), Visual Cortex (physiopathology), Visual Pathways (physiopathology).
- MESH :
- physiopathology : Brain Ischemia, Geniculate Bodies, Hallucinations, Nerve Net, Pons, REM Sleep Behavior Disorder, Stroke, Visual Cortex, Visual Pathways.
- Aged, Humans, Magnetic Resonance Imaging, Male, Polysomnography.
Abstract
Brainstem lesions causing peduncular hallucinosis (PH) produce vivid visual hallucinations occasionally accompanied by sleep disorders. Overlapping brainstem regions modulate visual pathways and REM sleep functions via gating of thalamocortical networks. A 66-year-old man with paroxysmal atrial fibrillation developed abrupt-onset complex visual hallucinations with preserved insight and violent dream enactment behavior. Brain MRI showed restricted diffusion in the left rostrodorsal pons suggestive of an acute ischemic stroke. REM sleep behavior disorder (RBD) was diagnosed on polysomnography. We investigated the integrity of ponto-geniculate-occipital circuits with seed-based resting-state functional connectivity MRI (rs-fcMRI) in this patient compared to 46 controls. Rs-fcMRI revealed significantly reduced functional connectivity between the lesion and lateral geniculate nuclei (LGN), and between LGN and visual association cortex compared to controls. Conversely, functional connectivity between brainstem and visual association cortex, and between visual association cortex and prefrontal cortex (PFC) was significantly increased in the patient. Focal damage to the rostrodorsal pons is sufficient to cause RBD and PH in humans, suggesting an overlapping mechanism in both syndromes. This lesion produced a pattern of altered functional connectivity consistent with disrupted visual cortex connectivity via de-afferentation of thalamocortical pathways.
DOI: 10.1016/j.cortex.2015.10.015
PubMed: 26656284
Affiliations:
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Geddes</name><affiliation wicri:level="2"><nlm:affiliation>Department of Brain and Cognitive Sciences and McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA; Brigham and Women's Hospital, Division of Cognitive and Behavioral Neurology, Harvard Medical School, Boston, MA, USA. Electronic address: mgeddes@mit.edu.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Brain and Cognitive Sciences and McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA; Brigham and Women's Hospital, Division of Cognitive and Behavioral Neurology, Harvard Medical School, Boston, MA</wicri:regionArea><placeName><region type="state">Massachusetts</region></placeName></affiliation></author><author><name sortKey="Tie, Yanmei" sort="Tie, Yanmei" uniqKey="Tie Y" first="Yanmei" last="Tie">Yanmei Tie</name><affiliation wicri:level="2"><nlm:affiliation>Brigham and Women's Hospital, Department of Neurosurgery, Harvard Medical School, Boston, MA, USA. Electronic address: ytie@partners.org.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Brigham and Women's Hospital, Department of Neurosurgery, Harvard Medical School, Boston, MA</wicri:regionArea><placeName><region type="state">Massachusetts</region></placeName></affiliation></author><author><name sortKey="Gabrieli, John D E" sort="Gabrieli, John D E" uniqKey="Gabrieli J" first="John D E" last="Gabrieli">John D E. Gabrieli</name><affiliation wicri:level="2"><nlm:affiliation>Department of Brain and Cognitive Sciences and McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA. Electronic address: gabrieli@mit.edu.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Brain and Cognitive Sciences and McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA</wicri:regionArea><placeName><region type="state">Massachusetts</region></placeName></affiliation></author><author><name sortKey="Mcginnis, Scott M" sort="Mcginnis, Scott M" uniqKey="Mcginnis S" first="Scott M" last="Mcginnis">Scott M. Mcginnis</name><affiliation wicri:level="2"><nlm:affiliation>Brigham and Women's Hospital, Division of Cognitive and Behavioral Neurology, Harvard Medical School, Boston, MA, USA. Electronic address: sm93@partners.org.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Brigham and Women's Hospital, Division of Cognitive and Behavioral Neurology, Harvard Medical School, Boston, MA</wicri:regionArea><placeName><region type="state">Massachusetts</region></placeName></affiliation></author><author><name sortKey="Golby, Alexandra J" sort="Golby, Alexandra J" uniqKey="Golby A" first="Alexandra J" last="Golby">Alexandra J. Golby</name><affiliation wicri:level="2"><nlm:affiliation>Brigham and Women's Hospital, Department of Neurosurgery, Harvard Medical School, Boston, MA, USA. Electronic address: agolby@partners.org.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Brigham and Women's Hospital, Department of Neurosurgery, Harvard Medical School, Boston, MA</wicri:regionArea><placeName><region type="state">Massachusetts</region></placeName></affiliation></author><author><name sortKey="Whitfield Gabrieli, Susan" sort="Whitfield Gabrieli, Susan" uniqKey="Whitfield Gabrieli S" first="Susan" last="Whitfield-Gabrieli">Susan Whitfield-Gabrieli</name><affiliation wicri:level="2"><nlm:affiliation>Department of Brain and Cognitive Sciences and McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA. Electronic address: swg@mit.edu.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Brain and Cognitive Sciences and McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA</wicri:regionArea><placeName><region type="state">Massachusetts</region></placeName></affiliation></author></analytic><series><title level="j">Cortex; a journal devoted to the study of the nervous system and behavior</title><idno type="eISSN">1973-8102</idno><imprint><date when="2016" type="published">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Brain Ischemia (physiopathology)</term><term>Geniculate Bodies (physiopathology)</term><term>Hallucinations (physiopathology)</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Nerve Net (physiopathology)</term><term>Polysomnography</term><term>Pons (physiopathology)</term><term>REM Sleep Behavior Disorder (physiopathology)</term><term>Stroke (physiopathology)</term><term>Visual Cortex (physiopathology)</term><term>Visual Pathways (physiopathology)</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Brain Ischemia</term><term>Geniculate Bodies</term><term>Hallucinations</term><term>Nerve Net</term><term>Pons</term><term>REM Sleep Behavior Disorder</term><term>Stroke</term><term>Visual Cortex</term><term>Visual Pathways</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Polysomnography</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Brainstem lesions causing peduncular hallucinosis (PH) produce vivid visual hallucinations occasionally accompanied by sleep disorders. Overlapping brainstem regions modulate visual pathways and REM sleep functions via gating of thalamocortical networks. A 66-year-old man with paroxysmal atrial fibrillation developed abrupt-onset complex visual hallucinations with preserved insight and violent dream enactment behavior. Brain MRI showed restricted diffusion in the left rostrodorsal pons suggestive of an acute ischemic stroke. REM sleep behavior disorder (RBD) was diagnosed on polysomnography. We investigated the integrity of ponto-geniculate-occipital circuits with seed-based resting-state functional connectivity MRI (rs-fcMRI) in this patient compared to 46 controls. Rs-fcMRI revealed significantly reduced functional connectivity between the lesion and lateral geniculate nuclei (LGN), and between LGN and visual association cortex compared to controls. Conversely, functional connectivity between brainstem and visual association cortex, and between visual association cortex and prefrontal cortex (PFC) was significantly increased in the patient. Focal damage to the rostrodorsal pons is sufficient to cause RBD and PH in humans, suggesting an overlapping mechanism in both syndromes. This lesion produced a pattern of altered functional connectivity consistent with disrupted visual cortex connectivity via de-afferentation of thalamocortical pathways.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26656284</PMID><DateCreated><Year>2016</Year><Month>01</Month><Day>24</Day></DateCreated><DateCompleted><Year>2017</Year><Month>01</Month><Day>10</Day></DateCompleted><DateRevised><Year>2017</Year><Month>02</Month><Day>20</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1973-8102</ISSN><JournalIssue CitedMedium="Internet"><Volume>74</Volume><PubDate><Year>2016</Year><Month>Jan</Month></PubDate></JournalIssue><Title>Cortex; a journal devoted to the study of the nervous system and behavior</Title><ISOAbbreviation>Cortex</ISOAbbreviation></Journal><ArticleTitle>Altered functional connectivity in lesional peduncular hallucinosis with REM sleep behavior disorder.</ArticleTitle><Pagination><MedlinePgn>96-106</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.cortex.2015.10.015</ELocationID><ELocationID EIdType="pii" ValidYN="Y">S0010-9452(15)00367-6</ELocationID><Abstract><AbstractText>Brainstem lesions causing peduncular hallucinosis (PH) produce vivid visual hallucinations occasionally accompanied by sleep disorders. Overlapping brainstem regions modulate visual pathways and REM sleep functions via gating of thalamocortical networks. A 66-year-old man with paroxysmal atrial fibrillation developed abrupt-onset complex visual hallucinations with preserved insight and violent dream enactment behavior. Brain MRI showed restricted diffusion in the left rostrodorsal pons suggestive of an acute ischemic stroke. REM sleep behavior disorder (RBD) was diagnosed on polysomnography. We investigated the integrity of ponto-geniculate-occipital circuits with seed-based resting-state functional connectivity MRI (rs-fcMRI) in this patient compared to 46 controls. Rs-fcMRI revealed significantly reduced functional connectivity between the lesion and lateral geniculate nuclei (LGN), and between LGN and visual association cortex compared to controls. Conversely, functional connectivity between brainstem and visual association cortex, and between visual association cortex and prefrontal cortex (PFC) was significantly increased in the patient. Focal damage to the rostrodorsal pons is sufficient to cause RBD and PH in humans, suggesting an overlapping mechanism in both syndromes. This lesion produced a pattern of altered functional connectivity consistent with disrupted visual cortex connectivity via de-afferentation of thalamocortical pathways.</AbstractText><CopyrightInformation>Crown Copyright © 2015. Published by Elsevier Ltd. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Geddes</LastName><ForeName>Maiya R</ForeName><Initials>MR</Initials><AffiliationInfo><Affiliation>Department of Brain and Cognitive Sciences and McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA; Brigham and Women's Hospital, Division of Cognitive and Behavioral Neurology, Harvard Medical School, Boston, MA, USA. Electronic address: mgeddes@mit.edu.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tie</LastName><ForeName>Yanmei</ForeName><Initials>Y</Initials><AffiliationInfo><Affiliation>Brigham and Women's Hospital, Department of Neurosurgery, Harvard Medical School, Boston, MA, USA. Electronic address: ytie@partners.org.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Gabrieli</LastName><ForeName>John D E</ForeName><Initials>JD</Initials><AffiliationInfo><Affiliation>Department of Brain and Cognitive Sciences and McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA. Electronic address: gabrieli@mit.edu.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>McGinnis</LastName><ForeName>Scott M</ForeName><Initials>SM</Initials><AffiliationInfo><Affiliation>Brigham and Women's Hospital, Division of Cognitive and Behavioral Neurology, Harvard Medical School, Boston, MA, USA. Electronic address: sm93@partners.org.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Golby</LastName><ForeName>Alexandra J</ForeName><Initials>AJ</Initials><AffiliationInfo><Affiliation>Brigham and Women's Hospital, Department of Neurosurgery, Harvard Medical School, Boston, MA, USA. Electronic address: agolby@partners.org.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Whitfield-Gabrieli</LastName><ForeName>Susan</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Department of Brain and Cognitive Sciences and McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA. Electronic address: swg@mit.edu.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>P41 EB015898</GrantID><Acronym>EB</Acronym><Agency>NIBIB NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R21 CA198740</GrantID><Acronym>CA</Acronym><Agency>NCI NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R21 NS075728</GrantID><Acronym>NS</Acronym><Agency>NINDS NIH HHS</Agency><Country>United States</Country></Grant><Grant><Agency>Canadian Institutes of Health Research</Agency><Country>Canada</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate 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MajorTopicYN="Y">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014795" MajorTopicYN="N">Visual Pathways</DescriptorName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading></MeshHeadingList><OtherID Source="NLM">NIHMS772193 [Available on 01/01/17]</OtherID><OtherID Source="NLM">PMC4820074 [Available on 01/01/17]</OtherID><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Hallucinations</Keyword><Keyword MajorTopicYN="N">Lateral geniculate nucleus</Keyword><Keyword MajorTopicYN="N">Lesion</Keyword><Keyword MajorTopicYN="N">Lewy body dementia</Keyword><Keyword MajorTopicYN="N">Pareidolia</Keyword><Keyword MajorTopicYN="N">Parkinson's disease</Keyword><Keyword MajorTopicYN="N">Prefrontal cortex</Keyword><Keyword MajorTopicYN="N">Resting state fMRI</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2015</Year><Month>05</Month><Day>24</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2015</Year><Month>08</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2015</Year><Month>10</Month><Day>23</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2015</Year><Month>12</Month><Day>15</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2015</Year><Month>12</Month><Day>15</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2017</Year><Month>1</Month><Day>11</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">26656284</ArticleId><ArticleId IdType="pii">S0010-9452(15)00367-6</ArticleId><ArticleId IdType="doi">10.1016/j.cortex.2015.10.015</ArticleId><ArticleId IdType="pmc">PMC4820074</ArticleId><ArticleId IdType="mid">NIHMS772193</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country><region><li>Massachusetts</li></region></list><tree><country name="États-Unis"><region name="Massachusetts"><name sortKey="Geddes, Maiya R" sort="Geddes, Maiya R" uniqKey="Geddes M" first="Maiya R" last="Geddes">Maiya R. Geddes</name></region><name sortKey="Gabrieli, John D E" sort="Gabrieli, John D E" uniqKey="Gabrieli J" first="John D E" last="Gabrieli">John D E. Gabrieli</name><name sortKey="Golby, Alexandra J" sort="Golby, Alexandra J" uniqKey="Golby A" first="Alexandra J" last="Golby">Alexandra J. Golby</name><name sortKey="Mcginnis, Scott M" sort="Mcginnis, Scott M" uniqKey="Mcginnis S" first="Scott M" last="Mcginnis">Scott M. Mcginnis</name><name sortKey="Tie, Yanmei" sort="Tie, Yanmei" uniqKey="Tie Y" first="Yanmei" last="Tie">Yanmei Tie</name><name sortKey="Whitfield Gabrieli, Susan" sort="Whitfield Gabrieli, Susan" uniqKey="Whitfield Gabrieli S" first="Susan" last="Whitfield-Gabrieli">Susan Whitfield-Gabrieli</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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