Insights into Biomarkers of Alzheimer's Disease: From Core Markers to Emerging Directions.

IF 6.9 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Weiyao Zhu, Yu Wang, Ming Qin, Qinghe Zhao, Lina Feng, Mingquan Li
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Abstract

Alzheimer's disease (AD) represents a neurodegenerative condition characterized by steadily increasing prevalence and incidence, arising significant challenge to both patients and social insurance. However, the etiology of AD remains controversial so far, and pathogenesis is far more complicated. Presently, no definitive therapeutic methodologies were available for AD, and only partial symptomatic relief can be achieved. Consequently, early diagnosis and intervention are emergently needed for AD patients. The diagnostic criteria for AD are continuously evolving, and biomarker testing is becoming increasingly critical for diagnosis. Currently, the diagnosis of AD primarily relies on the detection of pathological proteins through cerebrospinal fluid (CSF) testing and positron emission tomography (PET). However, factors such as high costs, operational contraindications, and invasiveness limited the application of these technologies, making them particularly challenging to implement in large-scale clinical trials and screenings. Core fluid biomarkers for AD including β-amyloid (Aβ), phosphorylated tau protein (p-tau), total tau protein (t-tau), and their combinations were found in CSF. Although these biomarkers were demonstrated with significant specificity and sensitivity, challenges remain high concerning the collection of CSF. Blood-derived biomarkers for Aβ and tau proteins are essential for preliminary screening, diagnosis, and monitoring of AD. Additionally, other bodily fluids such as saliva, urine, and tears have been investigated for their potential as biomarkers, offering unique characteristics and applications. Emerging biomarkers, including neurofilament light chain (NfL), neurogranin (Ng), Beta-site APP cleaving enzyme 1 (BACE1), synaptosome associated protein 25 (SNAP-25), as well as inflammation-related and gene-related factors, provided valuable insights into the diagnosis and pathogenesis of AD from diverse perspectives. Despite the substantial progress made in AD biomarker research, there are still baskets of limitations concerning the complication of the disease. The current review focused on the reported literature to summarize the biomarkers associated with AD. By critically analyzing studies published over the past decade, we aimed to strengthen the recent research progress, theoretical frameworks, and unresolved challenges related to AD biomarkers.

洞察阿尔茨海默病的生物标志物:从核心标志物到新兴方向。
阿尔茨海默病(AD)是一种神经退行性疾病,其特点是患病率和发病率稳步上升,对患者和社会保险都提出了重大挑战。然而,阿尔茨海默病的病因至今仍有争议,发病机制也要复杂得多。目前,阿尔茨海默病没有明确的治疗方法,只能部分缓解症状。因此,对AD患者的早期诊断和干预是迫切需要的。AD的诊断标准在不断发展,生物标志物检测在诊断中变得越来越重要。目前,AD的诊断主要依靠脑脊液(CSF)检测和正电子发射断层扫描(PET)检测病理蛋白。然而,诸如高成本、操作禁忌症和侵入性等因素限制了这些技术的应用,使其在大规模临床试验和筛查中实施尤其具有挑战性。在脑脊液中发现了AD的核心液体生物标志物,包括β-淀粉样蛋白(Aβ)、磷酸化tau蛋白(p-tau)、总tau蛋白(t-tau)及其组合。尽管这些生物标志物被证明具有显著的特异性和敏感性,但CSF的收集仍然存在很大的挑战。血液来源的Aβ和tau蛋白生物标志物对于AD的初步筛查、诊断和监测至关重要。此外,其他体液如唾液、尿液和眼泪也被研究作为生物标志物的潜力,提供独特的特性和应用。新兴的生物标志物,包括神经丝轻链(NfL)、神经粒蛋白(Ng)、β位点APP切割酶1 (BACE1)、突触体相关蛋白25 (SNAP-25),以及炎症相关和基因相关因子,从多个角度为AD的诊断和发病机制提供了有价值的见解。尽管阿尔茨海默病的生物标志物研究取得了实质性进展,但关于该疾病的并发症仍然存在许多局限性。本文综述了与AD相关的生物标志物的文献报道。通过批判性地分析过去十年发表的研究,我们旨在加强与AD生物标志物相关的最新研究进展、理论框架和未解决的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Aging and Disease
Aging and Disease GERIATRICS & GERONTOLOGY-
CiteScore
14.60
自引率
2.70%
发文量
138
审稿时长
10 weeks
期刊介绍: Aging & Disease (A&D) is an open-access online journal dedicated to publishing groundbreaking research on the biology of aging, the pathophysiology of age-related diseases, and innovative therapies for conditions affecting the elderly. The scope encompasses various diseases such as Stroke, Alzheimer's disease, Parkinson’s disease, Epilepsy, Dementia, Depression, Cardiovascular Disease, Cancer, Arthritis, Cataract, Osteoporosis, Diabetes, and Hypertension. The journal welcomes studies involving animal models as well as human tissues or cells.
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