Alzheimer's Imaging Consortium
3
Issued Date
2025-12-01
Resource Type
eISSN
15525279
Scopus ID
2-s2.0-105025737629
Pubmed ID
41433898
Journal Title
Alzheimer S Dementia the Journal of the Alzheimer S Association
Volume
21
Rights Holder(s)
SCOPUS
Bibliographic Citation
Alzheimer S Dementia the Journal of the Alzheimer S Association Vol.21 (2025) , e109936
Suggested Citation
Pongpitakmetha T., Taweephol T., Pornteparak N., Rianaree J., Ongphichetmetha T., Smitasiri T., Thanprasertsuk S., Chongsuksantikul A., Oangkhana P., Luechaipanit W., Haethaisong T., Khieukhajee J., Booncharoen K., Likitjaroen Y., Thanapornsangsuth P. Alzheimer's Imaging Consortium. Alzheimer S Dementia the Journal of the Alzheimer S Association Vol.21 (2025) , e109936. doi:10.1002/alz70862_109936 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/113731
Title
Alzheimer's Imaging Consortium
Corresponding Author(s)
Other Contributor(s)
Abstract
BACKGROUND: Cerebral small vessel disease (CSVD) is one of the leading causes of vascular cognitive impairment and dementia (VCID) in the aging population. It may also contribute to a faster rate of clinical deterioration in Alzheimer's disease (AD) as a co-pathology. Plasma glial fibrillary acidic protein (GFAP) may be elevated due to astrocytosis in either CSVD or AD pathogenesis. This study evaluates the correlation between CSVD neuroimaging biomarkers and plasma GFAP in a memory clinic cohort. METHODS: The clinical information and plasma biomarkers were collected from memory clinic cohorts. Patients were categorized into AD and non-AD groups based on either an abnormal cerebrospinal fluid Amyloid beta (Aβ) 42/p-tau181 ratio, or a positive Aβ Positron Emission Topography. Magnetic resonance imaging (MRI) was independently rated by the two trained investigators using STRIVE-2 criteria (Duering M, 2023). The validated composite total CSVD score (Staals J, 2014) ranging from 0-4 was calculated. The non-parametric statistical analysis was applied to analyze. RESULTS: A total of 114 participants were enrolled. Clinical information, laboratory test results, and neuroimaging biomarkers were compared between AD and non-AD groups, as shown in Table 1. A positive correlation exists between the total CSVD score and plasma GFAP in the whole and non-AD cohort (Spearman rho = 0.29, p-value 0.002). After the adjustment for plasma p-tau 217, the notable positive correlation between total CSVD score and plasma GFAP in the whole cohort (Spearman rho = 0.56, p-value < 0.001) is observed as demonstrated in visualized correlation plots in Figure 1. The results of Spearman's correlation and the Wilcoxon rank sum test between plasma GFAP and each neuroimaging biomarker are summarized in Table 2, where only certain neuroimaging biomarkers demonstrated a positive correlation. CONCLUSION: The total CSVD score and plasma GFAP showed a stronger positive correlation in the non-AD group than in the AD group. After adjusting for p-tau 217, an AD biomarker, the correlation between total CSVD score and plasma GFAP became stronger. These findings suggest that plasma GFAP alone may have limitations in assessing CSVD burden in AD due to shared mechanisms and biomarkers. Further validation of other potential VCID fluid biomarkers is warranted.