Prospective investigation of cerebellar cognitive affective syndrome in a previously non-demented population of acute cerebellar stroke

dc.contributor.author Taskiran-Sag, Aslihan
dc.contributor.author Uyanik, Handan Uzuncakmak
dc.contributor.author Uyanik, Sadik Ahmet
dc.contributor.author Oztekin, Nese
dc.date.accessioned 2024-05-25T12:29:45Z
dc.date.available 2024-05-25T12:29:45Z
dc.date.issued 2020
dc.description TASKIRAN SAG, Aslihan/0000-0001-7542-106X en_US
dc.description.abstract Objective: In this prospective study, we aimed to investigate the presence and evolu-tion of cerebellar cognitive affective syndrome in a cohort of isolated cerebellar stroke with no known cognitive or psychiatric impairment. We tried to distinguish the unconfounded effect of cerebellar lesions on neuropsychological processing. Methods: After a meticulous exclusion procedure based on possible confounders, we recruited 14 patients and 13 age-matched healthy controls to the study, prospec-tively. All of the patients had a detailed initial neuropsychological assessment at the first week and a follow-up assessment at the 4th month after stroke. Results: The prevalence of cognitive or behavioral-affective abnormalities in our cohort were 86% and 64% respectively. The patients exhibited mild and transient affective-behavioral abnormalities except for depressive symptoms that persisted in the sub-acute stage. They scored lower in general cognitive performance as revealed by mini mental test (p=0.001). Memory, executive functions, attention and working memory, central processing speed, and linguistic abilities were impaired (p<0.001; p=0.001; p=0.007; p=0.05; p<0.001 respectively). Improvement was evident only in memory domain of the cognitive functions in the subacute stage. Cognitive impairment was more likely with a medial or posterolateral infarct (p=0.014). Behavioral-affective abnormalities were not associated with a specific location in our cohort. Age seemed to negatively correlate with the recovery in general cogni-tive performance on the follow-up. Conclusions: These findings show that acute denervation of cerebellocortical projections leads to mild affective-behavioral abnormalities, and full-blown cerebellar cognitive affective syndrome is rare. How-ever, cognition was significantly affected after an acute cerebellar infarct even in a previously healthy, non-demented pure population. en_US
dc.identifier.citationcount 7
dc.identifier.doi 10.1016/j.jstrokecerebrovasdis.2020.104923
dc.identifier.issn 1052-3057
dc.identifier.issn 1532-8511
dc.identifier.scopus 2-s2.0-85085754668
dc.identifier.uri https://doi.org/10.1016/j.jstrokecerebrovasdis.2020.104923
dc.identifier.uri https://hdl.handle.net/20.500.14517/2137
dc.language.iso en
dc.publisher Elsevier en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Cerebellar cognitive affective syndrome en_US
dc.subject Schmahmann's syndrome en_US
dc.subject Cerebellum en_US
dc.subject Cognition en_US
dc.subject Stroke en_US
dc.title Prospective investigation of cerebellar cognitive affective syndrome in a previously non-demented population of acute cerebellar stroke en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id TASKIRAN SAG, Aslihan/0000-0001-7542-106X
gdc.author.scopusid 55982279000
gdc.author.scopusid 57216290122
gdc.author.scopusid 55072689200
gdc.author.scopusid 6603585539
gdc.author.wosid Sag, Aslihan Taskiran/AFP-4650-2022
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department Okan University en_US
gdc.description.departmenttemp [Taskiran-Sag, Aslihan; Oztekin, Nese] Ankara Numune Training & Res Hosp, Dept Neurol, TR-06100 Ankara, Turkey; [Uyanik, Handan Uzuncakmak] Kartal Dr Lutfi Kirdar Training & Res Hosp, Dept Neurol, Istanbul, Turkey; [Uyanik, Sadik Ahmet] Istanbul Okan Univ, Dept Radiol, Fac Med, Istanbul, Turkey en_US
gdc.description.issue 8 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.volume 29 en_US
gdc.description.wosquality Q3
gdc.identifier.pmid 32689613
gdc.identifier.wos WOS:000561808800010
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.scopus.citedcount 13
gdc.wos.citedcount 12

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