Association of MRI Visible Perivascular Spaces and Neurofilament Light Chain: The Framingham Heart Study

被引:1
|
作者
Ekenze, Oluchi [1 ,2 ]
Pinheiro, Adlin [2 ,3 ]
Demissie, Serkalem [2 ]
Aparicio, Hugo J. [2 ,4 ]
Charidimou, Andreas [4 ]
Beiser, Alexa S. [2 ,3 ,4 ]
Satizabal, Claudia L. [2 ,4 ,7 ]
Kautz, Tiffany [7 ]
DeCarli, Charles [8 ]
Greenberg, Steven [5 ]
Seshadri, Sudha [2 ,4 ,6 ,7 ]
Romero, Jose R. [2 ,4 ]
机构
[1] Boston Univ, Grad Med Sci, Sch Med, Boston, MA USA
[2] NHLBIs Framingham Heart Study, Framingham, MA USA
[3] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
[4] Boston Univ, Chobanian & Avedisian Sch Med, Dept Neurol, Boston, MA USA
[5] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Stroke Res, Dept Neurol, Boston, MA 02115 USA
[6] Univ Texas Hlth Sci Ctr, Glenn Biggs Inst Alzheimers & Neurodegenerat Dis, San Antonio, TX USA
[7] UT Hlth San Antonio, Dept Populat Hlth Sci, San Antonio, TX USA
[8] Univ Calif Davis, Dept Neurol, Davis, CA USA
关键词
Alzheimer's disease; basal ganglia; cerebral small vessel disease; MRI visible perivascular spaces; neurofilament light chain; neuroaxonal injury; SMALL VESSEL DISEASE; CEREBRAL AMYLOID ANGIOPATHY; MICROBLEEDS; BIOMARKERS;
D O I
10.3233/JAD-221260
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Neurofilament light chain (NfL) is a marker of neuronal injury. Perivascular spaces (PVS) visible on magnetic resonance imaging (MRI) represent cerebral small vessel disease (CSVD) but their role as markers of neuronal injury needs further clarification. Objective: To relate PVS burden according to brain topography and plasma NfL. Methods: Framingham Heart Study (FHS) participants with brain MRI and NfL measurements were included. PVS were rated in the basal ganglia (BG) and centrum semiovale (CSO) using validated methods and categorized based on counts. A mixed region variable representing high burden PVS in either BG or CSO was assessed. Multivariable linear regression analyses were used to relate PVS burden to log-transformed NfL levels in models adjusted for age, sex, FHS cohort, time between MRI and clinic exam, and image view (model 1), vascular risk factors (model 2), and white matter hyperintensity volume, covert brain infarcts, and cerebral microbleeds (model 3). Results: Among 1,457 participants (68.1 +/- 8.5 years, 45% males), NfL levels increased with higher PVS burden. Multivariable analysis showed an association of high PVS burden strictly in BG with NfL (beta = 0.117, 95% CI 0.014-0.221; p = 0.027), but attenuated in model 3. The associations were mainly in participants >= 65 years (beta = 0.122, 95% CI 0.015-0.229, p = 0.026), women (beta = 0.156, 95% CI 0.024-0.288, p = 0.021), and APOE epsilon 4 non-carriers (beta = 0.140, 95% CI 0.017-0.263, p = 0.026). Conclusions: The association of strictly BG high PVS burden with NfL suggests a role for PVS as markers of neuroaxonal injury, but our results are hypothesis generating and require further replication.
引用
收藏
页码:1133 / 1145
页数:13
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