Prognostic value of plasma biomarkers in early Alzheimer’s disease: a longitudinal clinical and neuroimaging study
Year: 2025
Type: article
Study design: Observational Study
Abstract: BACKGROUND: While blood biomarkers for AD have proven useful in identifying AD pathology from other neurodegenerative conditions, their prognostic value in real-world clinical settings, such as memory clinics, remains unexplored. We aimed to examine the prognostic value of AD plasma biomarkers and their short-term changes within 4 months, for predicting clinical and neuroradiological progression over two years. METHOD: We performed a prospective observational longitudinal cohort study of patients with early stages of AD and followed them for up to 2 years. Plasma was analysed for neurofilament light (NfL), brain-derived tau (BD-tau), phosphorylated tau 217 (p-tau217), and glial fibrillary acidic protein (GFAP) on single molecule array. The outcomes were annual changes in clinical dementia rating scale, sum of boxes (CDR-SB) and changes in [18F]-fluorodeoxyglucose positron emission tomography ([18F]FDG-PET) and magnetic resonance imaging (MRI) brain scans. We performed linear regression models with baseline and short-term plasma biomarker changes as predictors, adjusted for age, sex, and creatinine. RESULTS: In total, 94 patients with MCI or dementia due to AD had baseline and one-year follow-up, with 85 patients completing two-year follow-up. We found that baseline plasma NfL was significantly associated with an increase in CDR-SB at one- and two-year follow-up. Neither plasma BD-tau, p-tau217 or GFAP were associated with future clinical progression. Short-term changes of plasma NfL were associated with reduced glucose metabolism in the hippocampus and temporal cortex on [18F]FDG-PET. Short-term changes in plasma p-tau217 were significantly associated with reduced hippocampal glucose metabolism, and further, short-term changes in the p-tau217/BD-tau ratio were significantly associated with reduced metabolism in hippocampal and isthmus cingulate cortex on [18F]FDG-PET. We found no association between plasma biomarkers and MRI volumetric changes after multiple testing correction. CONCLUSION: Our findings indicate that plasma NfL can serve as a predictor for subsequent clinical progression in early AD. Short-term changes in AD-related plasma biomarkers may reflect underlying disease processes, however, several limitations affect their interpretability. Therefore, short-term changes should be evaluated carefully and always in the context of baseline levels and clinical characteristics. TRIAL REGISTRATION: Clinicaltrials.gov (NCT05175664), date of registration 2021–12-01.
Source: Alzheimer s Research & Therapy
Institutions: Copenhagen University Hospital, Rigshospitalet, University of Gothenburg, University of Wisconsin–Madison, Sahlgrenska University Hospital, UK Dementia Research Institute, UCL Queen Square Institute of Neurology, University College London, University of Science and Technology of China, Sorbonne Université, Institut des Sciences Moléculaires, Pitié-Salpêtrière Hospital, Institut du Cerveau, University of Copenhagen
Language: English
Subfield: Psychiatry and Mental health
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $4,290
Funders: Alzheimer's Association, Alzheimer's Drug Discovery Foundation, Familjen Erling-Perssons Stiftelse, Cure Alzheimer's Fund, Stiftelsen för Gamla Tjänarinnor, EU Joint Programme – Neurodegenerative Disease Research, National Institute for Health and Care Research, University College London, European Commission, Hjärnfonden, Vetenskapsrådet, A.P. Møller og Hustru Chastine Mc-Kinney Møllers Fond til almene Formaal, Direktør Emil C. Hertz og Hustru Inger Hertz Fond, Michaelsen Fonden, UK Dementia Research Institute, Fondation pour la Recherche sur Alzheimer, HORIZON EUROPE Framework Programme
Awards: G1057200632, G1088883541, G1135383168, G1222782219, G1311708188, G1373393710, G150733400, G1802301745, G1833008592, G2108271864, G2543812357, G2799940023, The Alzheimer biomarker toolbox – use in pathogenic studies, diagnostics and theragnostics, Fluid biomarkers for neurodegenerative dementias, G3548754657, G3903502641, G3914690605, G4181470480, G4234328627, G4260843567, G432431387, G434337789, G4377393254, G4404751248, G5040492720, G506008078, G516766298, Tau pathology in Alzheimer´s - understanding pathophysiology through biomarkers in blood and CSF, G5296150328, Fluid biomarkers for neurodegenerative dementias, G5619554209, CASCADE: CAuSe or Consequence in Alzheimer DiseasE?, G6142763750, G6158734006, G6168044258, Multi-omics Interdisciplinary Research Integration to Address DEmentia diagnosis, G6745400708, G7143958211, G7748812462
OpenAlex ID: W4416203584
