脑脊液
医学
神经退行性变
痴呆
疾病
萎缩
病理
认知功能衰退
神经科学
认知障碍
认知
生物标志物
生物信息学
癫痫
临床疾病
神经学
阿尔茨海默病
肿瘤科
中枢神经系统疾病
失智症
白质
内科学
磁共振成像
作者
Linbin Dai,Bjørn-Eivind Kirsebom,Chenxi Wang,Mengguo Zhang,Qiong Wang,Ming Ni,Fernando Gonzalez-Ortiz,K. Blennow,Jiong Shi,Tormod Fladby,Feng Gao,Yong Shen
标识
DOI:10.1038/s41467-026-70472-6
摘要
Identifying biomarkers that precisely track the neurodegenerative component of Alzheimer’s disease (AD) is essential for effective clinical management. Here we show that cerebrospinal fluid (CSF) levels of the synaptic proteins NPTX1 and NPTXR are robust indicators of disease severity and future clinical progression. In two independent, multi-ethnic cohorts spanning the AD continuum (n = 635), lower CSF NPTX levels correlate strongly with cognitive impairment and cortical thinning in AD-vulnerable regions. Longitudinally, baseline NPTX levels predict accelerated brain atrophy and the clinical transition from mild cognitive impairment to dementia, frequently outperforming or complementing established markers such as pTau181 and neurofilament light chain. These findings establish NPTX1 and NPTXR as sensitive, stage-specific markers of synaptic integrity and neurodegeneration. By accurately forecasting disease progression, these biomarkers offer significant potential to enhance patient stratification and provide a crucial tool for monitoring the efficacy of disease-modifying therapies in clinical trials. Researchers found that in China and Norway, cerebrospinal fluid NPTX1 and NPTXR drop as Alzheimer’s worsens, track brain thinning and cognition, and predict faster decline and conversion from mild cognitive impairment to dementia within 3 years.
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