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Role of Enlarged Perivascular Space in the Temporal Lobe in Cerebral Amyloidosis

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dc.contributor.authorNa, Han Kyu-
dc.contributor.authorKim, Han-Kyeol-
dc.contributor.authorLee, Hye Sun-
dc.contributor.authorPark, Mina-
dc.contributor.authorLee, Jae Hoon-
dc.contributor.authorRyu, Young Hoon-
dc.contributor.authorCho, Hanna-
dc.contributor.authorLyoo, Chul Hyoung-
dc.date.accessioned2023-07-12T03:13:54Z-
dc.date.available2023-07-12T03:13:54Z-
dc.date.created2023-07-12-
dc.date.issued2023-05-
dc.identifier.issn0364-5134-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/195543-
dc.description.abstractObjective Although growing evidence suggests that perivascular space (PVS) serves as a clearance route for amyloid and tau, the association between enlarged PVS (EPVS) and Alzheimer disease is highly inconsistent across studies. As the conventional visual rating systems for EPVS were insufficient to predict amyloid/tau/neurodegeneration (A/T/N) status, we developed a new rating scale for EPVS located in the temporal lobe (T-EPVS).Methods EPVS located in the basal ganglia (BG-EPVS), centrum semiovale (CS-EPVS), and T-EPVS was visually rated in 272 individuals (healthy controls, n = 96; mild cognitive impairment, n = 106; dementia, n = 70) who underwent structural magnetic resonance imaging (MRI) and dual positron emission tomography scans (F-18-flortaucipir and F-18-florbetaben). T-EPVS and BG-EPVS were defined as high degree when the counts in any hemisphere were > 10, and the CS-EPVS cutoff was > 20. Logistic regression models were constructed to investigate whether the regional EPVS burden was predictive of A/T/N status. The derived models were externally validated in a temporal validation cohort (n = 195) that underwent MRI studies using a different scanner.Results Compared with those with low-degree T-EPVS (23/136, 16.9%), individuals with high-degree T-EPVS/CS-EPVS but low-degree BG-EPVS were more likely to exhibit amyloid positivity (46/56, 82.1%). High-degree T-EPVS burden (odds ratio [OR] = 7.251, 95% confidence interval [CI] = 3.296-15.952) and low-degree BG-EPVS (OR = 0.241, 95% CI = 0.109-0.530) were predictive of amyloid positivity. Although high-degree T-EPVS was associated with tau positivity, the association was no longer significant after adjusting for amyloid and neurodegeneration status.Interpretation Investigating the burden and topographic distribution of EPVS including T-EPVS may be useful for predicting amyloid status, indicating that impaired perivascular drainage may contribute to cerebral amyloidosis.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherWiley-Liss-
dc.relation.isPartOfAnnals of Neurology-
dc.relation.isPartOfANNALS OF NEUROLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleRole of Enlarged Perivascular Space in the Temporal Lobe in Cerebral Amyloidosis-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurology (신경과학교실)-
dc.contributor.googleauthorNa, Han Kyu-
dc.contributor.googleauthorKim, Han-Kyeol-
dc.contributor.googleauthorLee, Hye Sun-
dc.contributor.googleauthorPark, Mina-
dc.contributor.googleauthorLee, Jae Hoon-
dc.contributor.googleauthorRyu, Young Hoon-
dc.contributor.googleauthorCho, Hanna-
dc.contributor.googleauthorLyoo, Chul Hyoung-
dc.identifier.doi10.1002/ana.26601-
dc.relation.journalcodeJ00166-
dc.identifier.eissn1531-8249-
dc.identifier.pmid36651566-
dc.contributor.alternativeNameKim, Han kyeol-
dc.contributor.affiliatedAuthorNa, Han Kyu-
dc.contributor.affiliatedAuthorKim, Han-Kyeol-
dc.contributor.affiliatedAuthorLee, Hye Sun-
dc.contributor.affiliatedAuthorPark, Mina-
dc.contributor.affiliatedAuthorLee, Jae Hoon-
dc.contributor.affiliatedAuthorRyu, Young Hoon-
dc.contributor.affiliatedAuthorCho, Hanna-
dc.contributor.affiliatedAuthorLyoo, Chul Hyoung-
dc.identifier.scopusid2-s2.0-85147347436-
dc.identifier.wosid000923327400001-
dc.citation.volume93-
dc.citation.number5-
dc.citation.startPage965-
dc.citation.endPage978-
dc.identifier.bibliographicCitationAnnals of Neurology, Vol.93(5) : 965-978, 2023-05-
dc.identifier.rimsid80163-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordPlusSMALL VESSEL-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusANGIOPATHY-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusMRI-
dc.subject.keywordPlusPET-
dc.subject.keywordPlusDEMENTIA-
dc.subject.keywordPlusTAU-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalResearchAreaNeurosciences & Neurology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Nuclear Medicine (핵의학교실) > 1. Journal Papers

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