Abstract
Background and Objectives: Neurodegeneration and vascular burden are the two most common causes of post-stroke cognitive impairment. However, the interrelationship between the plasma beta-amyloid (Aβ) and tau protein, cortical atrophy and brain amyloid accumulation on PET imaging in stroke patients is undetermined. We aimed to explore: (1) the relationships of cortical thickness and amyloid burden on PET with plasma Aβ40, Aβ42, tau protein and their composite scores in stroke patients; and (2) the associations of post-stroke cognitive presentations with these plasma and neuroimaging biomarkers.Methods: The prospective project recruited first-ever ischemic stroke patients around 3 months after stroke onset. The plasma Aβ40, Aβ42, and total tau protein were measured with the immunomagnetic reduction method. Cortical thickness was evaluated on MRI, and cortical amyloid plaque deposition was evaluated by 18F-florbetapir PET. Cognition was evaluated with Mini-Mental State Examination (MMSE), Geriatric Depression Scale (GDS), Dementia Rating Scale-2 (DRS-2).Results: The study recruited 24 stroke patients and 13 normal controls. The plasma tau and tau*Aβ42 levels were correlated with mean cortical thickness after age adjustment. The Aβ42/Aβ40 ratio was correlated with global cortical 18F-florbetapir uptake value. The DRS-2 and GDS scores were associated with mean cortical thickness and plasma biomarkers, including Aβ42/Aβ40, tau, tau*Aβ42, tau/Aβ42, and tau/Aβ40 levels, in stroke patients.Conclusion: Plasma Aβ, tau, and their composite scores were associated with cognitive performance 3 months after stroke, and these plasma biomarkers were correlated with corresponding imaging biomarkers of neurodegeneration. Further longitudinal studies with a larger sample size are warranted to replicate the study results.
Highlights
Neurodegeneration and vascular pathology are the two most common causes of cognitive impairment in the elderly
Cross-sectional study to screen patients with recent first-ever ischemic stroke from the Department of Neurology and Stroke Center at Linkou Chang Gung Memorial Hospital, Taiwan, as previously described (Huang et al, 2018b). These stroke patients were recruited based on the following criteria: (1) a diagnosis of acute ischemic stroke confirmed on magnetic resonance imaging (MRI) at stroke onset; (2) education years at least 6 years; (3) no history of old stroke, dementia, tauopathy diseases, substantial traumatic brain injury or epilepsy before the index stroke; (4) without recurrent stroke occurring between the index stroke and the study screening procedure; and (5) without persistent moderate to severe dysphasia, which was defined as a score of >1 point in the language score of the National Institutes of Health Stroke Scale (NIHSS; Srikanth et al, 2006)
Age was negatively correlated with mean cortical thickness in all participants (r = −0.35, p value = 0.04), and plasma tau protein level and tau-related composite scores were correlated with mean cortical thickness after age adjustment
Summary
Neurodegeneration and vascular pathology are the two most common causes of cognitive impairment in the elderly. Regarding the in vivo detection of neurodegenerative pathology in stroke patients, positron emission tomography (PET) imaging, cerebrospinal fluid (CSF) and blood examination have been developed in the past decades. Neurodegeneration and vascular burden are the two most common causes of post-stroke cognitive impairment. The interrelationship between the plasma beta-amyloid (Aβ) and tau protein, cortical atrophy and brain amyloid accumulation on PET imaging in stroke patients is undetermined. We aimed to explore: (1) the relationships of cortical thickness and amyloid burden on PET with plasma Aβ40, Aβ42, tau protein and their composite scores in stroke patients; and (2) the associations of post-stroke cognitive presentations with these plasma and neuroimaging biomarkers
Sign-in/Register to view highlights & summary Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
