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Background Mild Behavioral Impairment (MBI) has been increasingly recognized as a potential early clinical marker of neurodegenerative disease, while blood-based biomarkers such as phosphorylated tau 217 (p-tau217) and neurofilament light chain (NfL) are associated with Alzheimer’s disease and axonal damage, respectively. Objective To investigate the role of MBI and blood-based biomarkers of neurodegeneration in the early detection of dementia. Methods Fifty-one individuals without dementia aged 60 or older with mood or anxiety disorders underwent psychiatric, neuropsychiatric, and cognitive evaluations, as well as assessment of plasma p-tau217 and NfL at baseline and at one-year follow-up. Results A higher proportion of males was observed in the MBI group compared to the non-MBI group ( P = 0.076). MBI was significantly associated with a higher risk of conversion to dementia ( P = 0.006). MBI patients showed a trend toward higher baseline p-tau217 ( P = 0.096) and significantly higher NfL at follow-up ( P = 0.025), suggesting active neurodegeneration. Individuals who converted to dementia had marginally higher baseline p-tau217 ( P = 0.053) and NfL ( P = 0.091). Conclusion MBI and blood-based biomarkers of neurodegeneration appear to be promising clinical tools for identifying dementia risk in its early stages.
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Elefante et al. (2025) studied this question.
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