Brain Metabolic Correlates of Dopaminergic Denervation in Prodromal and Early Parkinson's Disease

Background It remains unclear how brain metabolic activities transform in response to dopamine deficiency in the prodromal and early phases of Parkinson's disease (PD). Objective To investigate the relationship between nigrostriatal dopaminergic denervation and brain glucose metabolism in patie...

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Veröffentlicht in:Movement disorders 2022-10, Vol.37 (10), p.2099-2109
Hauptverfasser: Kim, Ryul, Kim, Heejung, Kim, Yu Kyeong, Yoon, Eun Jin, Nam, Hyun Woo, Jeon, Beomseok, Lee, Jee‐Young
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container_end_page 2109
container_issue 10
container_start_page 2099
container_title Movement disorders
container_volume 37
creator Kim, Ryul
Kim, Heejung
Kim, Yu Kyeong
Yoon, Eun Jin
Nam, Hyun Woo
Jeon, Beomseok
Lee, Jee‐Young
description Background It remains unclear how brain metabolic activities transform in response to dopamine deficiency in the prodromal and early phases of Parkinson's disease (PD). Objective To investigate the relationship between nigrostriatal dopaminergic denervation and brain glucose metabolism in patients with isolated rapid eye movement sleep behavior disorder (iRBD) and early PD. Methods This cohort study included 28 patients with polysomnography‐confirmed iRBD, 24 patients with de novo PD with probable rapid eye movement sleep behavior disorder (denovoPD), and 28 healthy controls (HCs) who underwent two positron emission tomography scans with 18F‐fluorodeoxyglucose (all participants) and 18F‐N‐3‐fluoropropyl‐2β‐carboxymethoxy‐3β‐(4‐iodophenyl)‐nortropane (except for one denovoPD patient and 15 HCs). We analyzed striatal and voxel‐wise whole‐brain glucose metabolism in relation to nigrostriatal dopaminergic integrity and comparatively investigated the whole‐brain metabolic connectivity among the groups. We also assessed longitudinal metabolic changes against progressive dopaminergic denervation over 4 years in the iRBD group. Results From HCs to iRBD and finally to the denovoPD, dopaminergic integrity positively correlated with metabolic activity in the caudate, whereas a negative correlation was observed in the posterior putamen. In the iRBD group, there was a metabolic increase in the inferior orbitofrontal cortex against putaminal dopaminergic denervation at baseline, but negative correlations were newly observed in the superior orbitofrontal cortex and superior frontal gyrus at the 4‐year follow‐up. The denovoPD group showed negative correlations in the cerebellum and fusiform gyrus. Intra‐ and inter‐regional metabolic connectivities in the parieto‐occipital cortices were enhanced in the iRBD group compared with the denovoPD and HC groups. In the iRBD group, overall metabolic connectivity was strengthened along with enhanced basal ganglia‐frontal connection by advancing dopaminergic denervation. Conclusions Our findings suggest diverse trajectories of metabolic responses associated with dopaminergic denervation between individual brain areas in the prodromal and early PD stages. © 2022 International Parkinson and Movement Disorder Society.
doi_str_mv 10.1002/mds.29177
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Objective To investigate the relationship between nigrostriatal dopaminergic denervation and brain glucose metabolism in patients with isolated rapid eye movement sleep behavior disorder (iRBD) and early PD. Methods This cohort study included 28 patients with polysomnography‐confirmed iRBD, 24 patients with de novo PD with probable rapid eye movement sleep behavior disorder (denovoPD), and 28 healthy controls (HCs) who underwent two positron emission tomography scans with 18F‐fluorodeoxyglucose (all participants) and 18F‐N‐3‐fluoropropyl‐2β‐carboxymethoxy‐3β‐(4‐iodophenyl)‐nortropane (except for one denovoPD patient and 15 HCs). We analyzed striatal and voxel‐wise whole‐brain glucose metabolism in relation to nigrostriatal dopaminergic integrity and comparatively investigated the whole‐brain metabolic connectivity among the groups. We also assessed longitudinal metabolic changes against progressive dopaminergic denervation over 4 years in the iRBD group. Results From HCs to iRBD and finally to the denovoPD, dopaminergic integrity positively correlated with metabolic activity in the caudate, whereas a negative correlation was observed in the posterior putamen. In the iRBD group, there was a metabolic increase in the inferior orbitofrontal cortex against putaminal dopaminergic denervation at baseline, but negative correlations were newly observed in the superior orbitofrontal cortex and superior frontal gyrus at the 4‐year follow‐up. The denovoPD group showed negative correlations in the cerebellum and fusiform gyrus. Intra‐ and inter‐regional metabolic connectivities in the parieto‐occipital cortices were enhanced in the iRBD group compared with the denovoPD and HC groups. In the iRBD group, overall metabolic connectivity was strengthened along with enhanced basal ganglia‐frontal connection by advancing dopaminergic denervation. Conclusions Our findings suggest diverse trajectories of metabolic responses associated with dopaminergic denervation between individual brain areas in the prodromal and early PD stages. © 2022 International Parkinson and Movement Disorder Society.</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/mds.29177</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Basal ganglia ; Behavior disorders ; Cerebellum ; connectivity ; Cortex (frontal) ; Denervation ; dopamine ; Dopamine receptors ; Eye movements ; Frontal gyrus ; Glucose metabolism ; metabolic ; Metabolic response ; Metabolism ; Movement disorders ; Neostriatum ; Neural networks ; Neurodegenerative diseases ; Occipital lobe ; Parkinson's disease ; Positron emission tomography ; Putamen ; REM sleep ; REM sleep behavior disorder ; Sleep disorders</subject><ispartof>Movement disorders, 2022-10, Vol.37 (10), p.2099-2109</ispartof><rights>2022 International Parkinson and Movement Disorder Society.</rights><rights>2022 International Parkinson and Movement Disorder Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3307-51a5577b63374c7eaa3cb62acbd70dbc0b77a6fa9548e02f9ed86ada1ae7ca7b3</citedby><cites>FETCH-LOGICAL-c3307-51a5577b63374c7eaa3cb62acbd70dbc0b77a6fa9548e02f9ed86ada1ae7ca7b3</cites><orcidid>0000-0002-8754-9180 ; 0000-0002-9120-2075 ; 0000-0003-2491-3544</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmds.29177$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmds.29177$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Kim, Ryul</creatorcontrib><creatorcontrib>Kim, Heejung</creatorcontrib><creatorcontrib>Kim, Yu Kyeong</creatorcontrib><creatorcontrib>Yoon, Eun Jin</creatorcontrib><creatorcontrib>Nam, Hyun Woo</creatorcontrib><creatorcontrib>Jeon, Beomseok</creatorcontrib><creatorcontrib>Lee, Jee‐Young</creatorcontrib><title>Brain Metabolic Correlates of Dopaminergic Denervation in Prodromal and Early Parkinson's Disease</title><title>Movement disorders</title><description>Background It remains unclear how brain metabolic activities transform in response to dopamine deficiency in the prodromal and early phases of Parkinson's disease (PD). Objective To investigate the relationship between nigrostriatal dopaminergic denervation and brain glucose metabolism in patients with isolated rapid eye movement sleep behavior disorder (iRBD) and early PD. Methods This cohort study included 28 patients with polysomnography‐confirmed iRBD, 24 patients with de novo PD with probable rapid eye movement sleep behavior disorder (denovoPD), and 28 healthy controls (HCs) who underwent two positron emission tomography scans with 18F‐fluorodeoxyglucose (all participants) and 18F‐N‐3‐fluoropropyl‐2β‐carboxymethoxy‐3β‐(4‐iodophenyl)‐nortropane (except for one denovoPD patient and 15 HCs). We analyzed striatal and voxel‐wise whole‐brain glucose metabolism in relation to nigrostriatal dopaminergic integrity and comparatively investigated the whole‐brain metabolic connectivity among the groups. We also assessed longitudinal metabolic changes against progressive dopaminergic denervation over 4 years in the iRBD group. Results From HCs to iRBD and finally to the denovoPD, dopaminergic integrity positively correlated with metabolic activity in the caudate, whereas a negative correlation was observed in the posterior putamen. In the iRBD group, there was a metabolic increase in the inferior orbitofrontal cortex against putaminal dopaminergic denervation at baseline, but negative correlations were newly observed in the superior orbitofrontal cortex and superior frontal gyrus at the 4‐year follow‐up. The denovoPD group showed negative correlations in the cerebellum and fusiform gyrus. Intra‐ and inter‐regional metabolic connectivities in the parieto‐occipital cortices were enhanced in the iRBD group compared with the denovoPD and HC groups. In the iRBD group, overall metabolic connectivity was strengthened along with enhanced basal ganglia‐frontal connection by advancing dopaminergic denervation. Conclusions Our findings suggest diverse trajectories of metabolic responses associated with dopaminergic denervation between individual brain areas in the prodromal and early PD stages. © 2022 International Parkinson and Movement Disorder Society.</description><subject>Basal ganglia</subject><subject>Behavior disorders</subject><subject>Cerebellum</subject><subject>connectivity</subject><subject>Cortex (frontal)</subject><subject>Denervation</subject><subject>dopamine</subject><subject>Dopamine receptors</subject><subject>Eye movements</subject><subject>Frontal gyrus</subject><subject>Glucose metabolism</subject><subject>metabolic</subject><subject>Metabolic response</subject><subject>Metabolism</subject><subject>Movement disorders</subject><subject>Neostriatum</subject><subject>Neural networks</subject><subject>Neurodegenerative diseases</subject><subject>Occipital lobe</subject><subject>Parkinson's disease</subject><subject>Positron emission tomography</subject><subject>Putamen</subject><subject>REM sleep</subject><subject>REM sleep behavior disorder</subject><subject>Sleep disorders</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp10E1PwzAMBuAIgcQYHPgHkTgAh25J0zTtEdbxIW1iEnCu3NRFGW0zkg60f09ZOSFxsiU_tqyXkHPOJpyxcNqUfhKmXKkDMuJS8CAJpTokI5YkMhA8kcfkxPs1Y5xLHo8I3DowLV1iB4WtjaYz6xzW0KGntqKZ3UBjWnRv_SjDvvmEztiW9jsrZ0tnG6gptCWdg6t3dAXu3bTetpeeZsYjeDwlRxXUHs9-65i83s1fZg_B4un-cXazCLQQTAWSg5RKFbEQKtIKAYQu4hB0USpWFpoVSkFcQSqjBFlYpVgmMZTAAZUGVYgxuRrubpz92KLv8sZ4jXUNLdqtz0MVykikkRI9vfhD13br2v67veJJxFPZq-tBaWe9d1jlG2cacLucs_wn7LwPO9-H3dvpYL9Mjbv_Yb7MnoeNb2EhgXE</recordid><startdate>202210</startdate><enddate>202210</enddate><creator>Kim, Ryul</creator><creator>Kim, Heejung</creator><creator>Kim, Yu Kyeong</creator><creator>Yoon, Eun Jin</creator><creator>Nam, Hyun Woo</creator><creator>Jeon, Beomseok</creator><creator>Lee, Jee‐Young</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8754-9180</orcidid><orcidid>https://orcid.org/0000-0002-9120-2075</orcidid><orcidid>https://orcid.org/0000-0003-2491-3544</orcidid></search><sort><creationdate>202210</creationdate><title>Brain Metabolic Correlates of Dopaminergic Denervation in Prodromal and Early Parkinson's Disease</title><author>Kim, Ryul ; Kim, Heejung ; Kim, Yu Kyeong ; Yoon, Eun Jin ; Nam, Hyun Woo ; Jeon, Beomseok ; Lee, Jee‐Young</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3307-51a5577b63374c7eaa3cb62acbd70dbc0b77a6fa9548e02f9ed86ada1ae7ca7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Basal ganglia</topic><topic>Behavior disorders</topic><topic>Cerebellum</topic><topic>connectivity</topic><topic>Cortex (frontal)</topic><topic>Denervation</topic><topic>dopamine</topic><topic>Dopamine receptors</topic><topic>Eye movements</topic><topic>Frontal gyrus</topic><topic>Glucose metabolism</topic><topic>metabolic</topic><topic>Metabolic response</topic><topic>Metabolism</topic><topic>Movement disorders</topic><topic>Neostriatum</topic><topic>Neural networks</topic><topic>Neurodegenerative diseases</topic><topic>Occipital lobe</topic><topic>Parkinson's disease</topic><topic>Positron emission tomography</topic><topic>Putamen</topic><topic>REM sleep</topic><topic>REM sleep behavior disorder</topic><topic>Sleep disorders</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Ryul</creatorcontrib><creatorcontrib>Kim, Heejung</creatorcontrib><creatorcontrib>Kim, Yu Kyeong</creatorcontrib><creatorcontrib>Yoon, Eun Jin</creatorcontrib><creatorcontrib>Nam, Hyun Woo</creatorcontrib><creatorcontrib>Jeon, Beomseok</creatorcontrib><creatorcontrib>Lee, Jee‐Young</creatorcontrib><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Ryul</au><au>Kim, Heejung</au><au>Kim, Yu Kyeong</au><au>Yoon, Eun Jin</au><au>Nam, Hyun Woo</au><au>Jeon, Beomseok</au><au>Lee, Jee‐Young</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brain Metabolic Correlates of Dopaminergic Denervation in Prodromal and Early Parkinson's Disease</atitle><jtitle>Movement disorders</jtitle><date>2022-10</date><risdate>2022</risdate><volume>37</volume><issue>10</issue><spage>2099</spage><epage>2109</epage><pages>2099-2109</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>Background It remains unclear how brain metabolic activities transform in response to dopamine deficiency in the prodromal and early phases of Parkinson's disease (PD). Objective To investigate the relationship between nigrostriatal dopaminergic denervation and brain glucose metabolism in patients with isolated rapid eye movement sleep behavior disorder (iRBD) and early PD. Methods This cohort study included 28 patients with polysomnography‐confirmed iRBD, 24 patients with de novo PD with probable rapid eye movement sleep behavior disorder (denovoPD), and 28 healthy controls (HCs) who underwent two positron emission tomography scans with 18F‐fluorodeoxyglucose (all participants) and 18F‐N‐3‐fluoropropyl‐2β‐carboxymethoxy‐3β‐(4‐iodophenyl)‐nortropane (except for one denovoPD patient and 15 HCs). We analyzed striatal and voxel‐wise whole‐brain glucose metabolism in relation to nigrostriatal dopaminergic integrity and comparatively investigated the whole‐brain metabolic connectivity among the groups. We also assessed longitudinal metabolic changes against progressive dopaminergic denervation over 4 years in the iRBD group. Results From HCs to iRBD and finally to the denovoPD, dopaminergic integrity positively correlated with metabolic activity in the caudate, whereas a negative correlation was observed in the posterior putamen. In the iRBD group, there was a metabolic increase in the inferior orbitofrontal cortex against putaminal dopaminergic denervation at baseline, but negative correlations were newly observed in the superior orbitofrontal cortex and superior frontal gyrus at the 4‐year follow‐up. The denovoPD group showed negative correlations in the cerebellum and fusiform gyrus. Intra‐ and inter‐regional metabolic connectivities in the parieto‐occipital cortices were enhanced in the iRBD group compared with the denovoPD and HC groups. In the iRBD group, overall metabolic connectivity was strengthened along with enhanced basal ganglia‐frontal connection by advancing dopaminergic denervation. Conclusions Our findings suggest diverse trajectories of metabolic responses associated with dopaminergic denervation between individual brain areas in the prodromal and early PD stages. © 2022 International Parkinson and Movement Disorder Society.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><doi>10.1002/mds.29177</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-8754-9180</orcidid><orcidid>https://orcid.org/0000-0002-9120-2075</orcidid><orcidid>https://orcid.org/0000-0003-2491-3544</orcidid></addata></record>
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subjects Basal ganglia
Behavior disorders
Cerebellum
connectivity
Cortex (frontal)
Denervation
dopamine
Dopamine receptors
Eye movements
Frontal gyrus
Glucose metabolism
metabolic
Metabolic response
Metabolism
Movement disorders
Neostriatum
Neural networks
Neurodegenerative diseases
Occipital lobe
Parkinson's disease
Positron emission tomography
Putamen
REM sleep
REM sleep behavior disorder
Sleep disorders
title Brain Metabolic Correlates of Dopaminergic Denervation in Prodromal and Early Parkinson's Disease
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