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Effects of cerebrovascular disease and amyloid beta burden on cognition in subjects with subcortical vascular cognitive impairment

DC Field Value Language
dc.contributor.author김창수-
dc.date.accessioned2015-01-06T16:21:20Z-
dc.date.available2015-01-06T16:21:20Z-
dc.date.issued2014-
dc.identifier.issn0197-4580-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/97953-
dc.description.abstractCerebrovascular disease (CVD) and amyloid burden are the most frequent pathologies in subjects with cognitive impairment. However, the relationship between CVD, amyloid burden, and cognition are largely unknown. We aimed to evaluate whether CVD (lacunes, white matter hyperintensities, and microbleeds) and amyloid burden (Pittsburgh compound B [PiB] retention ratio) contribute to cognitive impairment independently or interactively. We recruited 136 patients with subcortical vascular cognitive impairment who underwent magnetic resonance imaging, PiB–positron emission tomography, and neuropsychological testing. The number of lacunes was associated with memory, frontal dysfunctions, and disease severity. The volume of white matter hyperintensities and the PiB retention ratio were associated only with memory dysfunction. There was no direct correlation between CVD markers and PiB retention ratio except that the number of lacunes was negatively correlated with the PiB retention ratio. In addition, there were no interactive effects of CVD and PiB retention ratio on cognition. Our findings suggest that CVD and amyloid burden contribute independently and not interactively to specific patterns of cognitive dysfunction in patients with subcortical vascular cognitive impairment.-
dc.description.statementOfResponsibilityopen-
dc.format.extent254~260-
dc.relation.isPartOfNEUROBIOLOGY OF AGING-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAmyloid beta-Peptides/metabolism*-
dc.subject.MESHAniline Compounds-
dc.subject.MESHBrain/diagnostic imaging-
dc.subject.MESHBrain/pathology-
dc.subject.MESHCerebrovascular Disorders/complications*-
dc.subject.MESHCognition Disorders/diagnosis-
dc.subject.MESHCognition Disorders/etiology*-
dc.subject.MESHCognition Disorders/metabolism-
dc.subject.MESHCognition Disorders/pathology-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMagnetic Resonance Imaging-
dc.subject.MESHMale-
dc.subject.MESHMemory Disorders/diagnosis-
dc.subject.MESHMemory Disorders/etiology-
dc.subject.MESHMemory Disorders/pathology-
dc.subject.MESHNeuropsychological Tests-
dc.subject.MESHPositron-Emission Tomography-
dc.subject.MESHThiazoles-
dc.titleEffects of cerebrovascular disease and amyloid beta burden on cognition in subjects with subcortical vascular cognitive impairment-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Preventive Medicine (예방의학)-
dc.contributor.googleauthorJae-Hyun Park-
dc.contributor.googleauthorSang Won Seo-
dc.contributor.googleauthorChangsoo Kim-
dc.contributor.googleauthorSook Hui Kim-
dc.contributor.googleauthorGeon Ha Kim-
dc.contributor.googleauthorSung Tae Kim-
dc.contributor.googleauthorSeun Jeon-
dc.contributor.googleauthorJong Min Lee-
dc.contributor.googleauthorSeung Jun Oh-
dc.contributor.googleauthorJae Seung Kim-
dc.contributor.googleauthorYearn Seong Choe-
dc.contributor.googleauthorKyung-Han Lee-
dc.contributor.googleauthorJi Soo Shin-
dc.contributor.googleauthorChi Hun Kim-
dc.contributor.googleauthorYoung Noh-
dc.contributor.googleauthorHanna Cho-
dc.contributor.googleauthorCindy W. Yoon-
dc.contributor.googleauthorHee Jin Kim-
dc.contributor.googleauthorByoung Seok Ye-
dc.contributor.googleauthorMichael Ewers-
dc.contributor.googleauthorMichael W. Weiner-
dc.contributor.googleauthorJae-Hong Lee-
dc.contributor.googleauthorDavid J. Werring-
dc.contributor.googleauthorDuk L. Na-
dc.identifier.doi10.1016/j.neurobiolaging.2013.06.026-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01042-
dc.relation.journalcodeJ02322-
dc.identifier.eissn1558-1497-
dc.identifier.pmid23932881-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S019745801300287X-
dc.subject.keywordAmyloid-
dc.subject.keywordCerebrovascular disease-
dc.subject.keywordCognition-
dc.subject.keywordLacune-
dc.subject.keywordMicrobleed-
dc.subject.keywordPittsburgh compound B-
dc.subject.keywordWhite matter hyperintensity-
dc.contributor.alternativeNameKim, Chang Soo-
dc.contributor.affiliatedAuthorKim, Chang Soo-
dc.rights.accessRightsfree-
dc.citation.volume35-
dc.citation.number1-
dc.citation.startPage254-
dc.citation.endPage260-
dc.identifier.bibliographicCitationNEUROBIOLOGY OF AGING, Vol.35(1) : 254-260, 2014-
dc.identifier.rimsid53449-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Preventive Medicine (예방의학교실) > 1. Journal Papers

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