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...
Gespeichert in:
Veröffentlicht in: | Movement disorders 2022-10, Vol.37 (10), p.2099-2109 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2725439473</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2725439473</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3307-51a5577b63374c7eaa3cb62acbd70dbc0b77a6fa9548e02f9ed86ada1ae7ca7b3</originalsourceid><addsrcrecordid>eNp10E1PwzAMBuAIgcQYHPgHkTgAh25J0zTtEdbxIW1iEnCu3NRFGW0zkg60f09ZOSFxsiU_tqyXkHPOJpyxcNqUfhKmXKkDMuJS8CAJpTokI5YkMhA8kcfkxPs1Y5xLHo8I3DowLV1iB4WtjaYz6xzW0KGntqKZ3UBjWnRv_SjDvvmEztiW9jsrZ0tnG6gptCWdg6t3dAXu3bTetpeeZsYjeDwlRxXUHs9-65i83s1fZg_B4un-cXazCLQQTAWSg5RKFbEQKtIKAYQu4hB0USpWFpoVSkFcQSqjBFlYpVgmMZTAAZUGVYgxuRrubpz92KLv8sZ4jXUNLdqtz0MVykikkRI9vfhD13br2v67veJJxFPZq-tBaWe9d1jlG2cacLucs_wn7LwPO9-H3dvpYL9Mjbv_Yb7MnoeNb2EhgXE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2725184195</pqid></control><display><type>article</type><title>Brain Metabolic Correlates of Dopaminergic Denervation in Prodromal and Early Parkinson's Disease</title><source>Wiley Online Library All Journals</source><creator>Kim, Ryul ; Kim, Heejung ; Kim, Yu Kyeong ; Yoon, Eun Jin ; Nam, Hyun Woo ; Jeon, Beomseok ; Lee, Jee‐Young</creator><creatorcontrib>Kim, Ryul ; Kim, Heejung ; Kim, Yu Kyeong ; Yoon, Eun Jin ; Nam, Hyun Woo ; Jeon, Beomseok ; Lee, Jee‐Young</creatorcontrib><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><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 & 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 & 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 & Medical Complete (Alumni)</collection><collection>Nursing & 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 & 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> |
fulltext | fulltext |
identifier | ISSN: 0885-3185 |
ispartof | Movement disorders, 2022-10, Vol.37 (10), p.2099-2109 |
issn | 0885-3185 1531-8257 |
language | eng |
recordid | cdi_proquest_miscellaneous_2725439473 |
source | Wiley Online Library All Journals |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T21%3A30%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Brain%20Metabolic%20Correlates%20of%20Dopaminergic%20Denervation%20in%20Prodromal%20and%20Early%20Parkinson's%20Disease&rft.jtitle=Movement%20disorders&rft.au=Kim,%20Ryul&rft.date=2022-10&rft.volume=37&rft.issue=10&rft.spage=2099&rft.epage=2109&rft.pages=2099-2109&rft.issn=0885-3185&rft.eissn=1531-8257&rft_id=info:doi/10.1002/mds.29177&rft_dat=%3Cproquest_cross%3E2725439473%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2725184195&rft_id=info:pmid/&rfr_iscdi=true |