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Sökning: id:"swepub:oai:gup.ub.gu.se/296423" > Baseline Results: T...

Baseline Results: The Association between Cardiovascular Risk and Preclinical Alzheimer's Disease Pathology (ASCEND) Study

Kumar, V. V. (författare)
Huang, H. (författare)
Zhao, L. (författare)
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Verble, D. D. (författare)
Nutaitis, A. (författare)
Tharwani, S. D. (författare)
Brown, A. L. (författare)
Zetterberg, Henrik, 1973 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Hu, W. (författare)
Shin, R. (författare)
Kehoe, P. G. (författare)
Quyyumi, A. (författare)
Nocera, J. (författare)
Kippels, A. (författare)
Wharton, W. (författare)
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 (creator_code:org_t)
2020
2020
Engelska.
Ingår i: Journal of Alzheimer's Disease. - 1387-2877. ; 75:1, s. 109-117
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: The rate of AD for African Americans (AAs) is 64% higher than for non-Hispanic White Americans (Whites). It is hypothesized that poor peripheral vascular function, in combination with genetics, stress, and inflammation may directly contribute to the accumulation of AD pathologic biomarkers. These risk factors may disproportionately affect AAs. Objective: Our objective was to determine if in a healthy middle-aged cohort at risk for AD (1) AD biomarkers in CSF differ by race, (2) peripheral vascular dysfunction and cognition are related to a higher burden of CSF AD biomarkers, and (3) these relationships differ by race. Methods: We enrolled 82 cognitively normal, middle-aged (45 and older) adults including AAs and Whites at high risk for AD due to parental history. Study procedures included lumbar puncture, vascular ultrasound, and cognitive testing. Results: While participants were in overall good health, AAs exhibited poorer indices of preclinical vascular health, including higher central SBP, central MAP, and EndoPAT AI, a marker of arterial stiffness. AAs also had significantly less cerebrospinal fluid tau burden than Whites. After polynomial regression analysis, adjusted for age, gender, education, and ApoE4 status, race significantly modified the relationship between total tau, phospho-tau, and Trails B, a marker of executive function. Small differences in tau correlated with poorer cognition in AAs. Conclusion: In a healthy middle-aged cohort at risk for AD, AAs had worse peripheral vascular health and worse cognition than Whites. Despite lower tau burden overall, race modified the relationship between tau and cognition, such that small differences in tau between AAs was related to worse cognition when compared to Whites. © 2020 - IOS Press and the authors. All rights reserved.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Psykiatri (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Psychiatry (hsv//eng)

Nyckelord

Alzheimer's disease
cognition
hypertension
parental history
prevention
tau
vascular risk
apolipoprotein E4
biological marker
adult
African American
aged
Alzheimer disease
arterial stiffness
Article
cardiovascular risk
Caucasian
cerebrospinal fluid
cohort analysis
disease association
executive function
female
follow up
human
longitudinal study
lumbar puncture
major clinical study
male
middle aged
neuropathology
observational study
peripheral vascular disease
priority journal
race difference
risk factor
task performance
ultrasound

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