Department of Pathophysiology, School of Basic Medicine, Key Laboratory of Education Ministry of China for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, PR China; Co-innovation Center of Neuroregeneration, Nantong University, Nantong, JS 226001, PR China; Cognitive Impairment Ward of Neurology Department, The Third Affiliated Hospital of Shenzhen University, 47 Youyi Rd., Shenzhen 518001, Guangdong Province, PR China.
Department of Pathophysiology, School of Basic Medicine, Key Laboratory of Education Ministry of China for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, PR China.
Ageing Res Rev. 2022 Feb;74:101544. doi: 10.1016/j.arr.2021.101544. Epub 2021 Dec 18.
Alzheimer's disease (AD), being the number one in terms of dementia burden, is an insidious age-related neurodegenerative disease and is presently considered a global public health threat. Its main histological hallmarks are the Aβ senile plaques and the P-tau neurofibrillary tangles, while clinically it is marked by a progressive cognitive decline that reflects the underlying synaptic loss and neurodegeneration. Many of the drug therapies targeting the two pathological hallmarks namely Aβ and P-tau have been proven futile. This is probably attributed to the initiation of therapy at a stage where cognitive alterations are already obvious. In other words, the underlying neuropathological changes are at a stage where these drugs lack any therapeutic value in reversing the damage. Therefore, there is an urgent need to start treatment in the very early stage where these changes can be reversed, and hence, early diagnosis is of primordial importance. To this aim, the use of robust and informative biomarkers that could provide accurate diagnosis preferably at an earlier phase of the disease is of the essence. To date, several biomarkers have been established that, to a different extent, allow researchers and clinicians to evaluate, diagnose, and more specially exclude other related pathologies. In this study, we extensively reviewed data on the currently explored biomarkers in terms of AD pathology-specific and non-specific biomarkers and highlighted the recent developments in the diagnostic and theragnostic domains. In the end, we have presented a separate elaboration on aspects of future perspectives and concluding remarks.
阿尔茨海默病(AD)是痴呆症负担最大的疾病,是一种隐匿的与年龄相关的神经退行性疾病,目前被认为是全球公共卫生威胁。其主要的组织学特征是 Aβ 老年斑和 P-tau 神经原纤维缠结,而临床上则以进行性认知能力下降为特征,反映了潜在的突触丧失和神经退行性变。许多针对 Aβ 和 P-tau 这两个病理标志物的药物治疗都被证明是无效的。这可能是由于在认知改变已经明显的阶段开始治疗。换句话说,在这些药物缺乏任何治疗价值来逆转损伤的情况下,潜在的神经病理学变化已经处于一个阶段。因此,迫切需要在这些变化可以逆转的早期阶段开始治疗,因此早期诊断至关重要。为此,使用强大且信息丰富的生物标志物来提供准确的诊断,最好是在疾病的早期阶段,这一点非常重要。迄今为止,已经确定了几种生物标志物,这些生物标志物在不同程度上允许研究人员和临床医生评估、诊断,特别是排除其他相关的病理。在这项研究中,我们广泛回顾了目前在 AD 病理学特异性和非特异性生物标志物方面探索的生物标志物的数据,并强调了诊断和治疗领域的最新发展。最后,我们对未来展望和结论的方面进行了单独的阐述。