Associations Between Vascular Risk Factors and Perivascular Spaces in Adults with Intact Cognition, Mild Cognitive Impairment, and Dementia

被引:1
|
作者
Rundek, Tatjana [1 ,2 ]
Del Brutto, Victor J. [2 ]
Goryawala, Mohammed [1 ,3 ]
Dong, Chuanhui [1 ,2 ]
Agudelo, Christian [1 ,2 ]
Saporta, Anita Seixas [1 ,2 ]
Merritt, Stacy [1 ,2 ]
Camargo, Christian [1 ,2 ]
Ariko, Taylor [1 ]
Loewenstein, David A. [1 ,4 ,5 ]
Duara, Ranjan [6 ]
Haq, Ihtsham [1 ,2 ]
机构
[1] Univ Miami, Miller Sch Med, Evelyn F McKnight Brain Inst, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Neurol, Miami, FL 33136 USA
[3] Univ Miami, Miller Sch Med, Dept Radiol, Miami, FL 33136 USA
[4] Univ Miami, Miller Sch Med, Ctr Neurocognit Sci & Aging, Miami, FL 33136 USA
[5] Univ Miami, Miller Sch Med, Dept Psychiat, Miami, FL 33136 USA
[6] Mt Sinai Med Ctr, Wien Ctr Alzheimers Dis & Memory Disorders, Miami Beach, FL 33140 USA
基金
美国国家卫生研究院;
关键词
Basal ganglia; brain MRI; centrum semiovale; perivascular spaces; vascular risk factors; SMALL-VESSEL DISEASE; VIRCHOW-ROBIN SPACES; CEREBRAL AMYLOID ANGIOPATHY; ALZHEIMERS-DISEASE; BLOOD-PRESSURE; BASAL GANGLIA; RATING-SCALE; MRI MARKERS; BRAIN; AGE;
D O I
10.3233/JAD-215585
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Perivascular spaces (PVS) are fluid-filled compartments surrounding small intracerebral vessels that transport fluid and clear waste. Objective: We examined associations between PVS count, vascular and neurodegenerative risk factors, and cognitive status among the predominantly Hispanic participants of the FL-VIP Study of Alzheimer's Disease Risk. Methods: Using brain MRI (n = 228), we counted PVS in single axial image through the basal ganglia (BG) and centrum semiovale (CSO). PVS per region were scored as 0 (none), 1 (<10), 2 (11-20), 3 (21-40), and 4 (>40). Generalized linear models examined PVS associations with vascular risk factors and a composite vascular comorbidity risk (VASCom) score. Results: Our sample (mean age 72 +/- 8 years, 61% women, 60% Hispanic, mean education 15 +/- 4 years, 33% APOE4 carriers) was 59% hypertensive, 21% diabetic, 66% hypercholesteremic, and 30% obese. Mean VASCom score was 2.3 +/- 1.6. PVS scores ranged from 0-4 in the BG (mean 1.3 +/- 0.7) and CSO (mean 1.2 +/- 0.9), and 0-7 combined (mean 2.5 +/- 1.4). In multivariable regression models, BG PVS was associated with age (beta = 0.03/year, p < 0.0001), Hispanic ethnicity (beta = 0.29, p =0 .01), education (beta= 0.04/year, p = 0.04), and coronary bypass surgery (beta = 0.93, p = 0.02). CSO PVS only associated with age (beta = 0.03/year, p < 0.01). APOE4 and amyloid-beta were not associated with PVS. Conclusion: BG PVS may be a marker of subclinical cerebrovascular disease. Further research is needed to validate associations and identify mechanisms linking BG PVS and cerebrovascular disease markers. PVS may be a marker of neurodegeneration despite our negative preliminary findings and more research is warranted. The association between BG PVS and Hispanic ethnicity also requires further investigation.
引用
收藏
页码:437 / 448
页数:12
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