单克隆抗体 (mAb) 作为阿尔茨海默病替代治疗方法的潜力:一项系统性范围研究

Nuraulia Aghnia Armansyah, Azalia Melati Putri, Wafiq Nurul Azizah, Ida Maryati
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引用次数: 0

摘要

阿尔茨海默病(AD)是一个全球性问题,预计将随着人口老龄化速度的加快而加剧。单克隆抗体(mAb)被认为能够克服淀粉样蛋白-β斑块的积累;淀粉样蛋白-β斑块是阿尔茨海默病的病理标志。本研究旨在探索 mAb 作为 AD 老年患者替代药物疗法的潜力。本研究采用了基于 PAGER 框架的范围综述设计。研究结果根据 PRISMA-ScR 协议进行鉴定,并使用 JBI 批判性评估核对表进行批评。文章检索通过 3 个数据库进行,包括 EBSCO-Host Academic Science Complete、PubMed 和 ScienceDirect,以及 3 个在线资源,包括 Sage Journals、Taylor Francis 和 Google Scholar。纳入标准为英文全文、主要研究文章、发表于 2018-2022 年间。综述共纳入 8 篇文章。大多数证据显示,6 种 mAbs 有可能减少 AD 患者体内淀粉样蛋白-β 的积累。单克隆抗体替代疗法的副作用是血管源性脑水肿和小脑出血或淀粉样蛋白相关成像异常(ARIA)的高发率。血浆 tau 有可能加强 AD 的临床诊断。使用 mAb 作为 AD 免疫疗法可以减少淀粉样蛋白-β,但副作用需要持续监测。mAb检查结果的差异可能受到临床诊断准确性较低的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential of Monoclonal Antibody (mAb) as Alternative Treatment of Alzheimer: A Sytematic Scoping Review
Alzheimer's disease (AD) is a global problem that is expected to increase along with the increasing rate of population aging. Monoclonal antibodies (mAb) are considered capable of overcoming the accumulation of amyloid-β plaques; pathological signs of AD. This study aims to explore the potential of mAbs as alternative pharmacological therapies for the elderly with AD. This study uses a scoping review design based on the PAGER framework. The results of the study were identified based on the PRISMA-ScR protocol and criticized using the JBI Critical Appraisal Checklist. Article searches were conducted through 3 databases including EBSCO-Host Academic Science Complete, PubMed, and ScienceDirect, and 3 online resources including Sage Journals, Taylor Francis, and Google Scholar. Inclusion criteria were full English text, primary research articles, and published between 2018-2022.A total of 8 articles were included in the review. Most of the evidence shows 6 mAbs have potential to reduce amyloid-β accumulation in AD patients. Alternative therapy with monoclonal antibodies has side effects that represent a major problem in the high incidence of vasogenic cerebral edema and micro cerebral hemorrhage or Amyloid Related Imaging Abnormalities (ARIA). Plasma tau has the potential to strengthen the clinical diagnosis of AD. The use of mAbs as AD immunotherapy can reduce amyloid-β with side effects that are monitored continuously. Differences in mAb examination results can be influenced by less accurate clinical diagnostic accuracy.
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