Roxanna Korologou-Linden, Ageing Epidemiology (AGE) Research Unit, School of Public Health, Imperial College London, 11th Floor, Charing Cross Hospital Campus, W6 8RP, Email:
J Prev Alzheimers Dis. 2024;11(4):897-902. doi: 10.14283/jpad.2024.83.
Recent positive trials for novel disease modifying therapies of anti-amyloid monoclonal antibodies represent a paradigm shift in the prevention and management of Alzheimer's disease, a relentlessly progressive and debilitating disease of old age. The reported efficacy of these new agents when given early in the disease trajectory is dependent on an early and accurate disease diagnosis, which is currently based on cerebrospinal fluid tests or/and neuro-imaging studies such as positron emission tomography. These confirmatory tests provide in vivo evidence of the pathological signature of Alzheimer's disease, of increased cerebral amyloid and tau burden and neurodegeneration. The emergence of blood-based biomarkers represents another breakthrough, offering a less invasive and scalable diagnostic tool that could be applied in both primary and specialist care settings, potentially revolutionizing Alzheimer's disease clinical pathways. However, healthcare systems face challenges in the adoption of these new technologies and therapies due to diagnostic and treatment capacity constraints, as well as financial and infrastructure requirements.
最近针对新型疾病修饰疗法(抗淀粉样蛋白单克隆抗体)的积极试验代表了阿尔茨海默病预防和管理的范式转变,阿尔茨海默病是一种无情进展和使人虚弱的老年疾病。这些新药物在疾病早期轨迹中使用的报告疗效取决于早期和准确的疾病诊断,目前基于脑脊液测试或/和神经影像学研究,如正电子发射断层扫描。这些确证性测试提供了阿尔茨海默病病理特征的体内证据,即大脑淀粉样蛋白和 tau 负担增加和神经退行性变。基于血液的生物标志物的出现代表了另一个突破,提供了一种侵入性较小且可扩展的诊断工具,可在初级和专科护理环境中应用,可能彻底改变阿尔茨海默病的临床路径。然而,由于诊断和治疗能力的限制以及财务和基础设施要求,医疗保健系统在采用这些新技术和疗法方面面临挑战。