Background: Changes in speech and language functions have shown to be early symptoms of AD pathology. Recent developments in automatic speech and language processing have opened avenues for objective assessments of these changes. The primary objective of this study is to explore whether speech and language markers extracted from cognitive testing conducted during an automated phone call differ according to underlying AD pathology as measured in cerebrospinal fluid (CSF) in preclinical or early stage individuals.
Method: Within the PROSPECT-AD project, speech and gold-standard clinical and biomarker data were obtained from the Beta-AARC cohort in Barcelona, Spain. The sample consisted of N = 41 cognitively unimpaired Spanish and Catalan speakers with Subjective Cognitive Decline. Speech features were extracted from phone recordings of the Rey Auditory Verbal Learning Task (RAVLT) and the Semantic Verbal Fluency Task (SVF). The Speech-Biomarker for Cognition (SB-C) was computed based on 43 temporal and semantic features. Based on established cutoffs, the sample was divided into amyloid beta 42 positive and negative and pTau positive and negative groups. Kruskal-Wallis tests were used to compare the positive and negative groups with regards to their overall cognition score and the SB-C subscores memory, executive function and processing speed for each of the CSF biomarkers respectively.
Results: The results of the group comparisons with regards to the amyloid beta 42 and pTau groups can be found in Table 1 and Table 2 respectively. Corresponding boxplots are presented in Figure 1. In summary, the amyloid beta negative group scored significantly higher on the SB-C than the amyloid beta positive group. In particular, the difference had a strong effect size for the processing speed subscore and a medium effect size for the executive function subscore. No significant difference was found with regards to the memory subscore. For the pTau groups, the difference in overall cognition score showed a trend towards significance.
Conclusion: This approach could establish a non-invasive and accessible means of identifying potential indicators of AD, contributing to early detection and timely intervention strategies.
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http://dx.doi.org/10.1002/alz.085181 | DOI Listing |
Adv Sci (Weinh)
January 2025
School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
β-secretase (BACE1) is instrumental in amyloid-β (Aβ) production, with overexpression noted in Alzheimer's disease (AD) neuropathology. The interaction of Aβ with the receptor for advanced glycation endproducts (RAGE) facilitates cerebral uptake of Aβ and exacerbates its neurotoxicity and neuroinflammation, further augmenting BACE1 expression. Given the limitations of previous BACE1 inhibition efforts, the study explores reducing BACE1 expression to mitigate AD pathology.
View Article and Find Full Text PDFNeurotherapeutics
January 2025
Department of Biochemistry, University of Alberta, Edmonton, Alberta, T6G 2H7, Canada. Electronic address:
Amyloidogenic protein aggregation is a pathological hallmark of Alzheimer's Disease (AD). As such, this critical feature of the disease has been instrumental in guiding research on the mechanistic basis of disease, diagnostic biomarkers and preventative and therapeutic treatments. Here we review identified molecular triggers and modulators of aggregation for two of the proteins associated with AD: amyloid beta and tau.
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January 2025
Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, School of Pharmaceutical Science and Technology, Faculty of Medicine, Tianjin University, Weijin Road, 300072 Tianjin, China. Electronic address:
Ethnopharmacological Relevance: Originally formulated to mitigate high-altitude sickness, Xinnaoxin capsules (XNX) are composed of three traditional Chinese medicines (Rhodiola rosea L., Lycium barbarum L. and Hippophae rhamnoides) with properties of anti-hypoxia, anti-fatigue, and anti-aging.
View Article and Find Full Text PDFMaturitas
January 2025
Institut du Vieillissement, Gérontopôle de Toulouse, Centre Hospitalo-Universitaire de Toulouse, 37 allées Jules Guesde, 31000 Toulouse, France; Institut Hospitalo-Universitaire HealthAge, Cité de la Santé, Place Lange, 31059 Toulouse, France; UMR INSERM, 1295 University of Toulouse III and Faculté de Médecine, 118 Rte de Narbonne, 31062 Toulouse, France.
This four-year longitudinal study investigated whether the cross-sectional and longitudinal associations of inflammation-related and neurodegenerative-related blood biomarkers with intrinsic capacity differ according to sex. The sample comprised 1117 older adults (<70 years, 63.8 % females) from the Multidomain Alzheimer's Prevention Trial (MAPT).
View Article and Find Full Text PDFMetab Brain Dis
January 2025
Department of Pharmacy, the Second Affiliated Hospital of Shaoyang University, Shaoyang, Hunan, China.
Alzheimer's disease (AD) is characterized by the accumulation of amyloid-β (Aβ) plaques and the aggregation of tau protein, resulting in intense memory loss and dementia. Diabetes-associated cognitive dysfunction (DACD) is a complication of diabetes mellitus, which is associated with decreased cognitive function and impaired memory. A growing body of literature emphasize the involvement of microglia in AD and DACD.
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