TY - JOUR
T1 - Comorbidity of Cerebrovascular and Alzheimer's Disease in Aging
AU - Xia, Ying
AU - Yassi, Nawaf
AU - Raniga, Parnesh
AU - Bourgeat, Pierrick
AU - Desmond, Patricia
AU - Doecke, James
AU - Ames, David
AU - Laws, Simon M.
AU - Fowler, Christopher
AU - Rainey-Smith, Stephanie R.
AU - Martins, Ralph
AU - Maruff, Paul
AU - Villemagne, Victor L.
AU - Masters, Colin L.
AU - Rowe, Christopher C.
AU - Fripp, Jurgen
AU - Salvado, Olivier
PY - 2020
Y1 - 2020
N2 - Background: Cerebrovascular disease often coexists with Alzheimer's disease (AD). While both diseases share common risk factors, their interrelationship remains unclear. Increasing the understanding of how cerebrovascular changes interact with AD is essential to develop therapeutic strategies and refine biomarkers for early diagnosis. Objective: We investigate the prevalence and risk factors for the comorbidity of amyloid-ß (Aß) and cerebrovascular disease in the Australian Imaging, Biomarkers and Lifestyle Study of Ageing, and further examine their cross-sectional association. Methods: A total of 598 participants (422 cognitively normal, 89 with mild cognitive impairment, 87 with AD) underwent positron emission tomography and structural magnetic resonance imaging for assessment of Aß deposition and cerebrovascular disease. Individuals were categorized based on the comorbidity status of Aß and cerebrovascular disease (V) as Aß-V-, Aß-V+, Aß+V-, or Aß+V+. Results: Advancing age was associated with greater likelihood of cerebrovascular disease, high Aß load and their comorbidity. Apolipoprotein E ?4 carriage was only associated with Aß positivity. Greater total and regional WMH burden were observed in participants with AD. However, no association were observed between Aß and WMH measures after stratification by clinical classification, suggesting that the observed association between AD and cerebrovascular disease was driven by the common risk factor of age. Conclusion: Our observations demonstrate common comorbid condition of Aß and cerebrovascular disease in later life. While our study did not demonstrate a convincing cross-sectional association between Aß and WMH burden, future longitudinal studies are required to further confirm this.
AB - Background: Cerebrovascular disease often coexists with Alzheimer's disease (AD). While both diseases share common risk factors, their interrelationship remains unclear. Increasing the understanding of how cerebrovascular changes interact with AD is essential to develop therapeutic strategies and refine biomarkers for early diagnosis. Objective: We investigate the prevalence and risk factors for the comorbidity of amyloid-ß (Aß) and cerebrovascular disease in the Australian Imaging, Biomarkers and Lifestyle Study of Ageing, and further examine their cross-sectional association. Methods: A total of 598 participants (422 cognitively normal, 89 with mild cognitive impairment, 87 with AD) underwent positron emission tomography and structural magnetic resonance imaging for assessment of Aß deposition and cerebrovascular disease. Individuals were categorized based on the comorbidity status of Aß and cerebrovascular disease (V) as Aß-V-, Aß-V+, Aß+V-, or Aß+V+. Results: Advancing age was associated with greater likelihood of cerebrovascular disease, high Aß load and their comorbidity. Apolipoprotein E ?4 carriage was only associated with Aß positivity. Greater total and regional WMH burden were observed in participants with AD. However, no association were observed between Aß and WMH measures after stratification by clinical classification, suggesting that the observed association between AD and cerebrovascular disease was driven by the common risk factor of age. Conclusion: Our observations demonstrate common comorbid condition of Aß and cerebrovascular disease in later life. While our study did not demonstrate a convincing cross-sectional association between Aß and WMH burden, future longitudinal studies are required to further confirm this.
KW - Alzheimer's disease
KW - amyloid
KW - cerebrovascular disease
KW - white matter hyperintensities
UR - http://www.scopus.com/inward/record.url?scp=85095119442&partnerID=8YFLogxK
U2 - 10.3233/JAD-200419
DO - 10.3233/JAD-200419
M3 - Article
C2 - 32986666
AN - SCOPUS:85095119442
SN - 1387-2877
VL - 78
SP - 321
EP - 334
JO - Journal of Alzheimer's Disease
JF - Journal of Alzheimer's Disease
IS - 1
ER -