Cerebrovascular disease in suspected non‐Alzheimer's pathophysiology and cognitive decline over time

التفاصيل البيبلوغرافية
العنوان: Cerebrovascular disease in suspected non‐Alzheimer's pathophysiology and cognitive decline over time
المؤلفون: Francis Nicole Saridin, Kimberly Ann Chew, Anthonin Reilhac, Bibek Gyanwali, Steven Gayoles Villaraza, Tomotaka Tanaka, Phillip Scheltens, Wiesje M. van der Flier, Christopher Li Hsian Chen, Saima Hilal
المساهمون: Neurology, Amsterdam Neuroscience - Neurodegeneration, APH - Personalized Medicine, APH - Methodology
المصدر: European Journal of Neurology, 29(7), 1922-1929. Wiley-Blackwell
Saridin, F N, Chew, K A, Reilhac, A, Gyanwali, B, Villaraza, S G, Tanaka, T, Scheltens, P, van der Flier, W M, Chen, C L H & Hilal, S 2022, ' Cerebrovascular disease in suspected non-Alzheimer's pathophysiology and cognitive decline over time ', European Journal of Neurology, vol. 29, no. 7, pp. 1922-1929 . https://doi.org/10.1111/ene.15337Test
بيانات النشر: Wiley, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Male, Amyloid beta-Peptides, Brain, Neuropsychological Tests, Magnetic Resonance Imaging, Cerebrovascular Disorders, Neurology, Alzheimer Disease, Positron-Emission Tomography, Humans, Cognitive Dysfunction, Female, Neurology (clinical), Biomarkers, Aged
الوصف: Background: The underlying cause of cognitive decline in individuals who are positive for biomarkers of neurodegeneration (N) but negative for biomarkers of amyloid-beta (A), designated as Suspected non-Alzheimer's pathophysiology (SNAP), remains unclear. We evaluate whether cerebrovascular disease (CeVD) is more prevalent in those with SNAP compared to A−N− and A+N+ individuals and whether CeVD is associated with cognitive decline over time in SNAP patients. Methods: A total of 216 individuals from a prospective memory clinic cohort (mean [SD] age, 72.7 [7.3] years, 100 women [56.5%]) were included and were diagnosed as no cognitive impairment (NCI), cognitive impairment no dementia (CIND), Alzheimer's dementia (AD) or vascular dementia (VaD). All individuals underwent clinical evaluation and neuropsychological assessment annually for up to 5 years. Carbon 11-labeled Pittsburgh Compound B ([11C]-PiB) or [18F]-flutafuranol-positron emission spectrometry imaging was performed to ascertain amyloid-beta status. Magnetic resonance imaging was performed to assess neurodegeneration as measured by medial temporal atrophy ≥2, as well as significant CeVD (sCeVD) burden, defined by cortical infarct count ≥1, Fazekas score ≥2, lacune count ≥2 or cerebral microbleed count ≥2. Results: Of the 216 individuals, 50 (23.1%) A−N+ were (SNAP), 93 (43.1%) A−N−, 36 (16.7%) A+N− and 37 (17.1%) A+N+. A+N+ individuals were significantly older, while A+N+ and SNAP individuals were more likely to have dementia. The SNAP group had a higher prevalence of sCeVD (90.0%) compared to A−N−. Moreover, SNAP individuals with sCeVD had significantly steeper decline in global cognition compared to A−N− over 5 years (p = 0.042). Conclusions: These findings suggest that CeVD is a contributing factor to cognitive decline in SNAP. Therefore, SNAP individuals should be carefully assessed and treated for CeVD.
تدمد: 1468-1331
1351-5101
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5693316d7e155f454d4ddf389a97b225Test
https://doi.org/10.1111/ene.15337Test
حقوق: RESTRICTED
رقم الانضمام: edsair.doi.dedup.....5693316d7e155f454d4ddf389a97b225
قاعدة البيانات: OpenAIRE