Work

Association of psychosis with cognitive impairment is mediated by amyloidopathy in cognitive impairment

Year: 2026

Type: article

Abstract: Background Psychosis, including delusions and hallucinations, is a significant neuropsychiatric symptom in Alzheimer’s disease (AD) associated with poor prognosis. The relationship between psychosis and AD pathology remains controversial. This study investigates the role of AD pathology in mediating the association between psychosis and cognitive impairment. Methods Data were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI). We included individuals with a Clinical Dementia Rating (CDR) score of 0.5 or higher. Among a total of 833 individuals, 96 individuals with psychosis were matched to 192 individuals without psychosis using propensity scores based on age, sex, education level, and follow-up duration. Baseline cognitive performance was assessed using composite memory scores (ADNI-MEM) and executive function scores (ADNI-EF). AD pathology was measured using baseline cerebralspinal fluid (CSF) levels of β -amyloid 1-42 (Aβ 1-42 ), hyperphosphorylated-tau 181 (p-tau 181 ), and total tau. Logistic regression was performed to evaluate the association of psychosis with baseline cognitive performance and CSF biomarkers. Mediation analysis was conducted to assess whether AD biomarkers mediate the relationship between cognitive impairment and psychosis. Results Psychosis was significantly associated with worse ADNI MEM score ( β = −0.622, p = 0.013) and worse ADNI EF score ( β = −0.516, p = 0.003), and lower CSF Aβ 1-42 levels ( β = −0.009, p = 0.007). No significant associations were found with p-tau 181 or total tau levels. Mediation analysis revealed that low CSF Aβ 1-42 levels mediated the relationship between cognitive impairment and psychosis. Conclusion These findings suggest that amyloid pathology may mediate the effect of baseline cognitive impairment on psychosis during disease in AD, highlighting a potential pathological link between cognitive decline and psychotic symptoms.

Source: Frontiers in Aging Neuroscience

DOI: 10.3389/fnagi.2025.1663120