Blandino Valeria, Colletti Tiziana, Ribisi Paolo, Tarantino Domenico, Mosca Viviana, Agnello Luisa, Ciaccio Marcello, Piccoli Tommaso
Cognitive and Memory Disorders Clinic, AOUP "Paolo Giaccone" University Teaching Hospital, Department of Biomedicine, Neurosciences, and Advanced Diagnostics (Bi.N.D.), University of Palermo, 90127 Palermo, Italy.
Institute of Clinical Biochemistry, Clinical Molecular Medicine, and Clinical Laboratory Medicine, Department of Biomedicine, Neurosciences, and Advanced Diagnostics (Bi.N.D), University of Palermo, 90127 Palermo, Italy.
Brain Sci. 2024 Sep 25;14(10):960. doi: 10.3390/brainsci14100960.
Alzheimer's disease (AD) is the most common neurodegenerative disorder and a leading cause of dementia. One major challenge for clinicians is accurately assessing the rate of disease progression (RoP) early in the diagnostic process, which is crucial for patient management and clinical trial stratification. This study evaluated the role of cerebrospinal fluid biomarkers-Aβ42, t-Tau, pTau, Neurogranin (Ng), and Neurofilament light-chain (NF-L)-in predicting RoP at the time of AD diagnosis. We included 56 AD patients and monitored cognitive impairment using MMSE scores at diagnosis and during six-month follow-up visits. RoP scores were calculated based on these assessments. Our correlation analyses revealed significant associations between RoP and pTau, Aβ42/Ng ratio, and NF-L levels. When patients were stratified by median RoP values into low-to-moderate (L-M: <2) and upper-moderate (U-M: >2) groups, those in the U-M group had notably higher CSF NF-L levels compared to the L-M group. Logistic regression analysis further demonstrated that elevated CSF NF-L levels were predictive of a faster RoP. These findings highlight the potential of CSF NF-L as a prognostic biomarker for rapid disease progression in AD. By identifying patients at risk for accelerated cognitive decline, CSF NF-L could significantly enhance early intervention strategies and improve patient management in clinical settings.
阿尔茨海默病(AD)是最常见的神经退行性疾病,也是痴呆症的主要病因。临床医生面临的一个主要挑战是在诊断过程早期准确评估疾病进展速度(RoP),这对患者管理和临床试验分层至关重要。本研究评估了脑脊液生物标志物——淀粉样前体蛋白42(Aβ42)、总tau蛋白(t-Tau)、磷酸化tau蛋白(pTau)、神经颗粒蛋白(Ng)和神经丝轻链(NF-L)——在AD诊断时预测RoP的作用。我们纳入了56例AD患者,并在诊断时和六个月的随访期间使用简易精神状态检查表(MMSE)评分监测认知障碍。基于这些评估计算RoP分数。我们的相关性分析揭示了RoP与pTau、Aβ42/Ng比值和NF-L水平之间存在显著关联。当根据RoP中位数将患者分为低至中度(L-M:<2)和中高(U-M:>2)组时,与L-M组相比,U-M组患者的脑脊液NF-L水平显著更高。逻辑回归分析进一步表明,脑脊液NF-L水平升高预示着RoP更快。这些发现凸显了脑脊液NF-L作为AD疾病快速进展预后生物标志物的潜力。通过识别有认知衰退加速风险的患者,脑脊液NF-L可显著加强早期干预策略并改善临床环境中的患者管理。