Araya Dimtsu Assfaw, Suzanne E Schindler, John C Morris
{"title":"Advances in blood biomarkers for Alzheimer disease (AD): A review.","authors":"Araya Dimtsu Assfaw, Suzanne E Schindler, John C Morris","doi":"10.1002/kjm2.12870","DOIUrl":null,"url":null,"abstract":"<p><p>Alzheimer disease (AD) and Alzheimer Disease and Related Dementias (AD/ADRD) are growing public health challenges globally affecting millions of older adults, necessitating concerted efforts to advance our understanding and management of these conditions. AD is a progressive neurodegenerative disorder characterized pathologically by amyloid plaques and tau neurofibrillary tangles that are the primary cause of dementia in older individuals. Early and accurate diagnosis of AD dementia is crucial for effective intervention and treatment but has proven challenging to accomplish. Although testing for AD brain pathology with cerebrospinal fluid (CSF) or positron emission tomography (PET) has been available for over 2 decades, most patients never underwent this testing because of inaccessibility, high out-of-pocket costs, perceived risks, and the lack of AD-specific treatments. However, in recent years, rapid progress has been made in developing blood biomarkers for AD/ADRD. Consequently, blood biomarkers have emerged as promising tools for non-invasive and cost-effective diagnosis, prognosis, and monitoring of AD progression. This review presents the evolving landscape of blood biomarkers in AD/ADRD and explores their potential applications in clinical practice for early detection, prognosis, and therapeutic interventions. It covers recent advances in blood biomarkers, including amyloid beta (Aβ) peptides, tau protein, neurofilament light chain (NfL), and glial fibrillary acidic protein (GFAP). It also discusses their diagnostic and prognostic utility while addressing associated challenges and limitations. Future research directions in this rapidly evolving field are also proposed.</p>","PeriodicalId":94244,"journal":{"name":"The Kaohsiung journal of medical sciences","volume":" ","pages":"692-698"},"PeriodicalIF":0.0000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Kaohsiung journal of medical sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/kjm2.12870","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/18 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Alzheimer disease (AD) and Alzheimer Disease and Related Dementias (AD/ADRD) are growing public health challenges globally affecting millions of older adults, necessitating concerted efforts to advance our understanding and management of these conditions. AD is a progressive neurodegenerative disorder characterized pathologically by amyloid plaques and tau neurofibrillary tangles that are the primary cause of dementia in older individuals. Early and accurate diagnosis of AD dementia is crucial for effective intervention and treatment but has proven challenging to accomplish. Although testing for AD brain pathology with cerebrospinal fluid (CSF) or positron emission tomography (PET) has been available for over 2 decades, most patients never underwent this testing because of inaccessibility, high out-of-pocket costs, perceived risks, and the lack of AD-specific treatments. However, in recent years, rapid progress has been made in developing blood biomarkers for AD/ADRD. Consequently, blood biomarkers have emerged as promising tools for non-invasive and cost-effective diagnosis, prognosis, and monitoring of AD progression. This review presents the evolving landscape of blood biomarkers in AD/ADRD and explores their potential applications in clinical practice for early detection, prognosis, and therapeutic interventions. It covers recent advances in blood biomarkers, including amyloid beta (Aβ) peptides, tau protein, neurofilament light chain (NfL), and glial fibrillary acidic protein (GFAP). It also discusses their diagnostic and prognostic utility while addressing associated challenges and limitations. Future research directions in this rapidly evolving field are also proposed.
阿尔茨海默病(AD)和阿尔茨海默病及相关痴呆症(AD/ADRD)是全球日益严峻的公共卫生挑战,影响着数百万老年人,因此有必要共同努力,增进我们对这些疾病的了解和管理。老年痴呆症是一种进行性神经退行性疾病,病理特征为淀粉样蛋白斑块和 tau 神经纤维缠结,是导致老年人痴呆的主要原因。早期准确诊断 AD 痴呆症对于有效干预和治疗至关重要,但事实证明要做到这一点却很困难。尽管利用脑脊液(CSF)或正电子发射断层扫描(PET)检测阿德氏病大脑病理已有二十多年的历史,但由于交通不便、自付费用高、认为存在风险以及缺乏针对阿德氏病的治疗方法,大多数患者从未接受过这种检测。然而,近年来,AD/ADRD 血液生物标志物的开发取得了快速进展。因此,血液生物标志物已成为无创、经济有效的诊断、预后判断和AD进展监测的理想工具。本综述介绍了 AD/ADRD 血液生物标志物的发展状况,并探讨了它们在临床实践中用于早期检测、预后判断和治疗干预的潜在应用。它涵盖了血液生物标志物的最新进展,包括淀粉样β(Aβ)肽、tau蛋白、神经丝轻链(NfL)和神经胶质纤维酸性蛋白(GFAP)。报告还讨论了它们在诊断和预后方面的效用,同时探讨了相关的挑战和局限性。此外,还提出了这一快速发展领域的未来研究方向。