痴呆
神经退行性变
认知功能衰退
医学
生物标志物
疾病
萧条(经济学)
心情
精神科
焦虑
内科学
阿尔茨海默病
情绪障碍
认知
失智症
肿瘤科
认知障碍
认知障碍
共病
神经学
退行性疾病
临床心理学
老年精神病学
作者
Camilla Elefante,Maria Francesca Beatino,Chiara Fustini,Vittoria Lepri,Donatella Acierno,Alessia Scalzo,Lucia Petrozzi,Linda Giampietri,Gloria Tognoni,Filippo Baldacci,Lorenzo Lattanzi,Gabriele Siciliano,Zahinoor Ismail,Roberto Ceravolo,Giulio Perugi
标识
DOI:10.1177/08919887251394747
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI