Significance of hyposmia in isolated REM sleep behavior disorder

Objective To determine if hyposmia in isolated REM sleep behavior disorder (IRBD) predicts short-term conversion to any α-synucleinopathy and declines with time. Methods Olfaction was tested using the University of Pennsylvania Smell Identification Test (UPSIT-40) in 140 consecutive patients with po...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of neurology 2021-03, Vol.268 (3), p.963-966
Hauptverfasser: Iranzo, Alex, Marrero-González, Paula, Serradell, Mónica, Gaig, Carles, Santamaria, Joan, Vilaseca, Isabel
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 966
container_issue 3
container_start_page 963
container_title Journal of neurology
container_volume 268
creator Iranzo, Alex
Marrero-González, Paula
Serradell, Mónica
Gaig, Carles
Santamaria, Joan
Vilaseca, Isabel
description Objective To determine if hyposmia in isolated REM sleep behavior disorder (IRBD) predicts short-term conversion to any α-synucleinopathy and declines with time. Methods Olfaction was tested using the University of Pennsylvania Smell Identification Test (UPSIT-40) in 140 consecutive patients with polysomnography-confirmed IRBD and in 77 matched controls. Patients were followed-up during 5.6 ± 3.9 (range 0.2–13) years. Twenty-one patients underwent serial UPSIT-40 evaluations at 1–3 and 4–6 years after baseline. Results UPSIT-40 score was lower in patients than in controls (20.2 ± 6.5 vs. 28.6 ± 5.0; p  
doi_str_mv 10.1007/s00415-020-10229-3
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2445967125</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2445967125</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-894f8993140634e091caf7fbd1e8a0c6e96a3a68e4b9f180c4caca5c7b94ff563</originalsourceid><addsrcrecordid>eNp9kEtLAzEUhYMotlb_gAsZcONm9OYxM8lOKb6gIvhYh0zmRlOmMzVpBf-9sa0KLlxlcb5zknyEHFI4pQDVWQQQtMiBQU6BMZXzLTKkgrOcikJtkyFwAXnBCzEgezFOAUCmYJcMOFOlVFwNyfmjf-m889Z0FrPeZa8f8z7OvMl8l_nYt2aBTfZweZfFFnGe1fhq3n0fsiaFocGwT3acaSMebM4Reb66fBrf5JP769vxxSS3vCoWuVTCSaU4FVBygaCoNa5ydUNRGrAlqtJwU0oUtXJUghXWWFPYqk5FV5R8RE7Wu_PQvy0xLvTMR4ttazrsl1Ezkb5WVpQVCT3-g077ZejS6xKluJSMrSi2pmzoYwzo9Dz4mQkfmoL-8qvXfnXyq1d-NU-lo830sp5h81P5FpoAvgZiiroXDL93_zP7Cd56hGE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2493882225</pqid></control><display><type>article</type><title>Significance of hyposmia in isolated REM sleep behavior disorder</title><source>SpringerLink Journals - AutoHoldings</source><creator>Iranzo, Alex ; Marrero-González, Paula ; Serradell, Mónica ; Gaig, Carles ; Santamaria, Joan ; Vilaseca, Isabel</creator><creatorcontrib>Iranzo, Alex ; Marrero-González, Paula ; Serradell, Mónica ; Gaig, Carles ; Santamaria, Joan ; Vilaseca, Isabel</creatorcontrib><description>Objective To determine if hyposmia in isolated REM sleep behavior disorder (IRBD) predicts short-term conversion to any α-synucleinopathy and declines with time. Methods Olfaction was tested using the University of Pennsylvania Smell Identification Test (UPSIT-40) in 140 consecutive patients with polysomnography-confirmed IRBD and in 77 matched controls. Patients were followed-up during 5.6 ± 3.9 (range 0.2–13) years. Twenty-one patients underwent serial UPSIT-40 evaluations at 1–3 and 4–6 years after baseline. Results UPSIT-40 score was lower in patients than in controls (20.2 ± 6.5 vs. 28.6 ± 5.0; p  &lt; 0.001). Hyposmia (UPSIT-40 score &lt; 19 points) occurred in 42.9% patients. Forty-three (30.7%) patients developed Parkinson disease (PD = 27), dementia with Lewy bodies (DLB = 13) and multiple system atrophy (MSA = 3). Kaplan–Meier analysis showed that hyposmics had higher risk than normosmics to develop a synucleinopathy at the short term ( p  = 0.030). UPSIT-40 score was similar between patients who developed PD and DLB ( p  = 0.136). Normal smell occurred in all three (100%) IRBD patients who developed MSA, 12 of 27 (44%) who developed PD, and 4 of 13 (31%) that developed DLB. Serial UPSIT-40 evaluations showed no changes with time ( p  = 0.518). Conclusion In IRBD, hyposmia is a short-term risk for synucleinopathies but cannot distinguish underlying PD from DLB. Normosmia not only occurs in latent MSA but also in latent PD and DLB. In future IRBD neuroprotective trails, individuals at entry could be enriched for hyposmia, whereas serial evaluation of smell would not be useful to monitor the efficacy of a therapeutic intervention.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-020-10229-3</identifier><identifier>PMID: 32968939</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Atrophy ; Behavior disorders ; Dementia disorders ; Lewy bodies ; Medicine ; Medicine &amp; Public Health ; Movement disorders ; Neurodegenerative diseases ; Neurology ; Neuroprotection ; Neuroradiology ; Neurosciences ; Olfaction ; Olfaction disorders ; Original Communication ; Parkinson's disease ; REM sleep ; Sleep disorders</subject><ispartof>Journal of neurology, 2021-03, Vol.268 (3), p.963-966</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-894f8993140634e091caf7fbd1e8a0c6e96a3a68e4b9f180c4caca5c7b94ff563</citedby><cites>FETCH-LOGICAL-c375t-894f8993140634e091caf7fbd1e8a0c6e96a3a68e4b9f180c4caca5c7b94ff563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00415-020-10229-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00415-020-10229-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32968939$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iranzo, Alex</creatorcontrib><creatorcontrib>Marrero-González, Paula</creatorcontrib><creatorcontrib>Serradell, Mónica</creatorcontrib><creatorcontrib>Gaig, Carles</creatorcontrib><creatorcontrib>Santamaria, Joan</creatorcontrib><creatorcontrib>Vilaseca, Isabel</creatorcontrib><title>Significance of hyposmia in isolated REM sleep behavior disorder</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Objective To determine if hyposmia in isolated REM sleep behavior disorder (IRBD) predicts short-term conversion to any α-synucleinopathy and declines with time. Methods Olfaction was tested using the University of Pennsylvania Smell Identification Test (UPSIT-40) in 140 consecutive patients with polysomnography-confirmed IRBD and in 77 matched controls. Patients were followed-up during 5.6 ± 3.9 (range 0.2–13) years. Twenty-one patients underwent serial UPSIT-40 evaluations at 1–3 and 4–6 years after baseline. Results UPSIT-40 score was lower in patients than in controls (20.2 ± 6.5 vs. 28.6 ± 5.0; p  &lt; 0.001). Hyposmia (UPSIT-40 score &lt; 19 points) occurred in 42.9% patients. Forty-three (30.7%) patients developed Parkinson disease (PD = 27), dementia with Lewy bodies (DLB = 13) and multiple system atrophy (MSA = 3). Kaplan–Meier analysis showed that hyposmics had higher risk than normosmics to develop a synucleinopathy at the short term ( p  = 0.030). UPSIT-40 score was similar between patients who developed PD and DLB ( p  = 0.136). Normal smell occurred in all three (100%) IRBD patients who developed MSA, 12 of 27 (44%) who developed PD, and 4 of 13 (31%) that developed DLB. Serial UPSIT-40 evaluations showed no changes with time ( p  = 0.518). Conclusion In IRBD, hyposmia is a short-term risk for synucleinopathies but cannot distinguish underlying PD from DLB. Normosmia not only occurs in latent MSA but also in latent PD and DLB. In future IRBD neuroprotective trails, individuals at entry could be enriched for hyposmia, whereas serial evaluation of smell would not be useful to monitor the efficacy of a therapeutic intervention.</description><subject>Atrophy</subject><subject>Behavior disorders</subject><subject>Dementia disorders</subject><subject>Lewy bodies</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Movement disorders</subject><subject>Neurodegenerative diseases</subject><subject>Neurology</subject><subject>Neuroprotection</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Olfaction</subject><subject>Olfaction disorders</subject><subject>Original Communication</subject><subject>Parkinson's disease</subject><subject>REM sleep</subject><subject>Sleep disorders</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kEtLAzEUhYMotlb_gAsZcONm9OYxM8lOKb6gIvhYh0zmRlOmMzVpBf-9sa0KLlxlcb5zknyEHFI4pQDVWQQQtMiBQU6BMZXzLTKkgrOcikJtkyFwAXnBCzEgezFOAUCmYJcMOFOlVFwNyfmjf-m889Z0FrPeZa8f8z7OvMl8l_nYt2aBTfZweZfFFnGe1fhq3n0fsiaFocGwT3acaSMebM4Reb66fBrf5JP769vxxSS3vCoWuVTCSaU4FVBygaCoNa5ydUNRGrAlqtJwU0oUtXJUghXWWFPYqk5FV5R8RE7Wu_PQvy0xLvTMR4ttazrsl1Ezkb5WVpQVCT3-g077ZejS6xKluJSMrSi2pmzoYwzo9Dz4mQkfmoL-8qvXfnXyq1d-NU-lo830sp5h81P5FpoAvgZiiroXDL93_zP7Cd56hGE</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Iranzo, Alex</creator><creator>Marrero-González, Paula</creator><creator>Serradell, Mónica</creator><creator>Gaig, Carles</creator><creator>Santamaria, Joan</creator><creator>Vilaseca, Isabel</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20210301</creationdate><title>Significance of hyposmia in isolated REM sleep behavior disorder</title><author>Iranzo, Alex ; Marrero-González, Paula ; Serradell, Mónica ; Gaig, Carles ; Santamaria, Joan ; Vilaseca, Isabel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-894f8993140634e091caf7fbd1e8a0c6e96a3a68e4b9f180c4caca5c7b94ff563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Atrophy</topic><topic>Behavior disorders</topic><topic>Dementia disorders</topic><topic>Lewy bodies</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Movement disorders</topic><topic>Neurodegenerative diseases</topic><topic>Neurology</topic><topic>Neuroprotection</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Olfaction</topic><topic>Olfaction disorders</topic><topic>Original Communication</topic><topic>Parkinson's disease</topic><topic>REM sleep</topic><topic>Sleep disorders</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iranzo, Alex</creatorcontrib><creatorcontrib>Marrero-González, Paula</creatorcontrib><creatorcontrib>Serradell, Mónica</creatorcontrib><creatorcontrib>Gaig, Carles</creatorcontrib><creatorcontrib>Santamaria, Joan</creatorcontrib><creatorcontrib>Vilaseca, Isabel</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health &amp; Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health &amp; Nursing</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><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iranzo, Alex</au><au>Marrero-González, Paula</au><au>Serradell, Mónica</au><au>Gaig, Carles</au><au>Santamaria, Joan</au><au>Vilaseca, Isabel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Significance of hyposmia in isolated REM sleep behavior disorder</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>268</volume><issue>3</issue><spage>963</spage><epage>966</epage><pages>963-966</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><abstract>Objective To determine if hyposmia in isolated REM sleep behavior disorder (IRBD) predicts short-term conversion to any α-synucleinopathy and declines with time. Methods Olfaction was tested using the University of Pennsylvania Smell Identification Test (UPSIT-40) in 140 consecutive patients with polysomnography-confirmed IRBD and in 77 matched controls. Patients were followed-up during 5.6 ± 3.9 (range 0.2–13) years. Twenty-one patients underwent serial UPSIT-40 evaluations at 1–3 and 4–6 years after baseline. Results UPSIT-40 score was lower in patients than in controls (20.2 ± 6.5 vs. 28.6 ± 5.0; p  &lt; 0.001). Hyposmia (UPSIT-40 score &lt; 19 points) occurred in 42.9% patients. Forty-three (30.7%) patients developed Parkinson disease (PD = 27), dementia with Lewy bodies (DLB = 13) and multiple system atrophy (MSA = 3). Kaplan–Meier analysis showed that hyposmics had higher risk than normosmics to develop a synucleinopathy at the short term ( p  = 0.030). UPSIT-40 score was similar between patients who developed PD and DLB ( p  = 0.136). Normal smell occurred in all three (100%) IRBD patients who developed MSA, 12 of 27 (44%) who developed PD, and 4 of 13 (31%) that developed DLB. Serial UPSIT-40 evaluations showed no changes with time ( p  = 0.518). Conclusion In IRBD, hyposmia is a short-term risk for synucleinopathies but cannot distinguish underlying PD from DLB. Normosmia not only occurs in latent MSA but also in latent PD and DLB. In future IRBD neuroprotective trails, individuals at entry could be enriched for hyposmia, whereas serial evaluation of smell would not be useful to monitor the efficacy of a therapeutic intervention.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32968939</pmid><doi>10.1007/s00415-020-10229-3</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0340-5354
ispartof Journal of neurology, 2021-03, Vol.268 (3), p.963-966
issn 0340-5354
1432-1459
language eng
recordid cdi_proquest_miscellaneous_2445967125
source SpringerLink Journals - AutoHoldings
subjects Atrophy
Behavior disorders
Dementia disorders
Lewy bodies
Medicine
Medicine & Public Health
Movement disorders
Neurodegenerative diseases
Neurology
Neuroprotection
Neuroradiology
Neurosciences
Olfaction
Olfaction disorders
Original Communication
Parkinson's disease
REM sleep
Sleep disorders
title Significance of hyposmia in isolated REM sleep behavior disorder
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T22%3A04%3A17IST&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=Significance%20of%20hyposmia%20in%20isolated%20REM%20sleep%20behavior%20disorder&rft.jtitle=Journal%20of%20neurology&rft.au=Iranzo,%20Alex&rft.date=2021-03-01&rft.volume=268&rft.issue=3&rft.spage=963&rft.epage=966&rft.pages=963-966&rft.issn=0340-5354&rft.eissn=1432-1459&rft_id=info:doi/10.1007/s00415-020-10229-3&rft_dat=%3Cproquest_cross%3E2445967125%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=2493882225&rft_id=info:pmid/32968939&rfr_iscdi=true