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Distinct Cognitive Trajectories According to Amyloid Positivity in Non-Alzheimer Disease Dementias

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dc.contributor.author전민영-
dc.date.accessioned2025-02-03T08:31:26Z-
dc.date.available2025-02-03T08:31:26Z-
dc.date.issued2024-12-
dc.identifier.issn0363-9762-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/201719-
dc.description.abstractBackground: The clinical effects of β-amyloid positivity (Aβ+) on copathologies in various dementias remain relatively underexamined. Thus, the present study was conducted to investigate the prevalence and clinical effects of Aβ+ in subcortical vascular cognitive impairment (SVCI) and frontotemporal dementia (FTD). Patients and methods: We enrolled SVCI (n = 583), FTD (n = 152), and cognitively unimpaired (CU) participants (n = 1,249) who underwent Aβ PET scans. The odds of having Aβ+ were subsequently compared among the diagnostic groups (CU, SVCI, and FTD) according to age and apolipoprotein E genotype. Additionally, a linear mixed-effects model was used to investigate the effects of Aβ+ on cognitive trajectories in SVCI and FTD. Results: Compared with CU, the SVCI group had a higher prevalence of Aβ+ in the 75 to 90 years age group (adjusted odds ratio, 1.97; 95% confidence interval, 1.36-2.85; P < 0.001), as well as within the apolipoprotein E ε3/ε3 group (adjusted odds ratio, 1.78; 95% confidence interval, 1.20-2.63; P = 0.001), whereas the FTD group showed no difference in Aβ+ prevalence. Aβ+ was associated with a worse cognitive trajectory in SVCI (adjusted β-coefficient = -0.6424; P < 0.001), but not in FTD. Conclusions: These findings contribute to our understanding of Aβ biomarker traits in various dementias in Korea.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherLippincott-
dc.relation.isPartOfCLINICAL NUCLEAR MEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAlzheimer Disease / diagnostic imaging-
dc.subject.MESHAlzheimer Disease / metabolism-
dc.subject.MESHAmyloid / metabolism-
dc.subject.MESHAmyloid beta-Peptides / metabolism-
dc.subject.MESHApolipoproteins E / genetics-
dc.subject.MESHCognition-
dc.subject.MESHDementia* / diagnostic imaging-
dc.subject.MESHDementia* / metabolism-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPositron-Emission Tomography-
dc.titleDistinct Cognitive Trajectories According to Amyloid Positivity in Non-Alzheimer Disease Dementias-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurology (신경과학교실)-
dc.contributor.googleauthorHyemin Jang-
dc.contributor.googleauthorMin Young Chun-
dc.contributor.googleauthorJihwan Yun-
dc.contributor.googleauthorJun Pyo Kim-
dc.contributor.googleauthorSung Hoon Kang-
dc.contributor.googleauthorHee Jin Kim-
dc.contributor.googleauthorDuk L Na-
dc.contributor.googleauthorEun Hye Lee-
dc.contributor.googleauthorDaeun Shin-
dc.contributor.googleauthorHongki Ham-
dc.contributor.googleauthorYuna Gu-
dc.contributor.googleauthorChi-Hun Kim-
dc.contributor.googleauthorSook-Young Woo-
dc.contributor.googleauthorSang Won Seo-
dc.contributor.googleauthorK-ROAD Study Groups-
dc.identifier.doi10.1097/RLU.0000000000005457-
dc.contributor.localIdA06416-
dc.relation.journalcodeJ00595-
dc.identifier.eissn1536-0229-
dc.identifier.pmid39385364-
dc.identifier.urlhttps://journals.lww.com/nuclearmed/fulltext/2024/12000/distinct_cognitive_trajectories_according_to.1.aspx-
dc.contributor.alternativeNameChun, Min Young-
dc.contributor.affiliatedAuthor전민영-
dc.citation.volume49-
dc.citation.number12-
dc.citation.startPage1073-
dc.citation.endPage1078-
dc.identifier.bibliographicCitationCLINICAL NUCLEAR MEDICINE, Vol.49(12) : 1073-1078, 2024-12-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers

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