Comorbidity of Cerebrovascular and Alzheimer's Disease in Aging

被引:8
|
作者
Xia, Ying [1 ]
Yassi, Nawaf [2 ,3 ,4 ]
Raniga, Parnesh [1 ]
Bourgeat, Pierrick [1 ]
Desmond, Patricia [5 ]
Doecke, James [1 ]
Ames, David [6 ,7 ]
Laws, Simon M. [8 ,9 ,10 ]
Fowler, Christopher [4 ]
Rainey-Smith, Stephanie R. [8 ,10 ]
Martins, Ralph [8 ,10 ]
Maruff, Paul [4 ,11 ]
Villemagne, Victor L. [4 ,12 ,13 ,14 ]
Masters, Colin L. [4 ]
Rowe, Christopher C. [12 ,13 ,14 ]
Fripp, Jurgen [1 ]
Salvado, Olivier [1 ,15 ]
机构
[1] CSIRO Hlth & Biosecur, Australian E Hlth Res Ctr, Brisbane, Qld, Australia
[2] Univ Melbourne, Melbourne Brain Ctr, Dept Med & Neurol, Royal Melbourne Hosp, Parkville, Vic, Australia
[3] Populat Hlth & Immun Div, Walter & Eliza Hall Inst Med Res, Parkville, Vic, Australia
[4] Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia
[5] Univ Melbourne, Royal Melbourne Hosp, Dept Radiol, Parkville, Vic, Australia
[6] Natl Ageing Res Inst, Parkville, Vic, Australia
[7] Univ Melbourne, Acad Unit Psychiat Old Age, Parkville, Vic, Australia
[8] Edith Cowan Univ, Ctr Excellence Alzheimers Dis Res & Care, Sch Med & Hlth Sci, Joondalup, WA, Australia
[9] Curtin Univ, Fac Hlth Sci, Sch Pharm & Biomed Sci, Curtin Hlth Innovat Res Inst, Bentley, WA, Australia
[10] Hollywood Private Hosp, Sir James McCusker Alzheimers Dis Res Unit, Perth, WA, Australia
[11] Cog State Ltd, Melbourne, Vic, Australia
[12] Austin Hlth, Dept Nucl Med, Heidelberg, Vic, Australia
[13] Austin Hlth, Ctr Pet, Heidelberg, Vic, Australia
[14] Univ Melbourne, Dept Med, Austin Hlth, Heidelberg, Vic, Australia
[15] CSIRO Data6l, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
Alzheimer's disease; amyloid; cerebrovascular disease; white matter hyperintensities; MILD COGNITIVE IMPAIRMENT; WHITE-MATTER HYPERINTENSITIES; AMYLOID-BETA; LESIONS; PATHOLOGIES; PERFORMANCE; PREVALENCE; DEMENTIA; INFARCTS; DECLINE;
D O I
10.3233/JAD-200419
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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-beta (A beta) 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 A beta deposition and cerebrovascular disease. Individuals were categorized based on the comorbidity status of A beta and cerebrovascular disease (V) as A beta-V-, A beta-V+, A beta+V-, or A beta+V+. Results: Advancing age was associated with greater likelihood of cerebrovascular disease, high A beta load and their comorbidity. Apolipoprotein E epsilon 4 carriage was only associated with A beta positivity. Greater total and regional WMH burden were observed in participants with AD. However, no association were observed between A beta 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 A beta and cerebrovascular disease in later life. While our study did not demonstrate a convincing cross-sectional association between A beta and WMH burden, future longitudinal studies are required to further confirm this.
引用
收藏
页码:321 / 334
页数:14
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