{"title":"Current potential diagnostic biomarkers of amyotrophic lateral sclerosis.","authors":"Zheqi Xu, Renshi Xu","doi":"10.1515/revneuro-2024-0037","DOIUrl":null,"url":null,"abstract":"<p><p>Amyotrophic lateral sclerosis (ALS) currently lacks the useful diagnostic biomarkers. The current diagnosis of ALS is mainly depended on the clinical manifestations, which contributes to the diagnostic delay and be difficult to make the accurate diagnosis at the early stage of ALS, and hinders the clinical early therapeutics. The more and more pathogenesis of ALS are found at the last 30 years, including excitotoxicity, the oxidative stress, the mitochondrial dysfunction, neuroinflammation, the altered energy metabolism, the RNA misprocessing and the most recent neuroimaging findings. The findings of these pathogenesis bring the new clues for searching the diagnostic biomarkers of ALS. At present, a large number of relevant studies about the diagnostic biomarkers are underway. The ALS pathogenesis related to the diagnostic biomarkers might lessen the diagnostic reliance on the clinical manifestations. Among them, the cortical altered signatures of ALS patients derived from both structural and functional magnetic resonance imaging and the emerging proteomic biomarkers of neuronal loss and glial activation in the cerebrospinal fluid as well as the potential biomarkers in blood, serum, urine, and saliva are leading a new phase of biomarkers. Here, we reviewed these current potential diagnostic biomarkers of ALS.</p>","PeriodicalId":49623,"journal":{"name":"Reviews in the Neurosciences","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reviews in the Neurosciences","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1515/revneuro-2024-0037","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Amyotrophic lateral sclerosis (ALS) currently lacks the useful diagnostic biomarkers. The current diagnosis of ALS is mainly depended on the clinical manifestations, which contributes to the diagnostic delay and be difficult to make the accurate diagnosis at the early stage of ALS, and hinders the clinical early therapeutics. The more and more pathogenesis of ALS are found at the last 30 years, including excitotoxicity, the oxidative stress, the mitochondrial dysfunction, neuroinflammation, the altered energy metabolism, the RNA misprocessing and the most recent neuroimaging findings. The findings of these pathogenesis bring the new clues for searching the diagnostic biomarkers of ALS. At present, a large number of relevant studies about the diagnostic biomarkers are underway. The ALS pathogenesis related to the diagnostic biomarkers might lessen the diagnostic reliance on the clinical manifestations. Among them, the cortical altered signatures of ALS patients derived from both structural and functional magnetic resonance imaging and the emerging proteomic biomarkers of neuronal loss and glial activation in the cerebrospinal fluid as well as the potential biomarkers in blood, serum, urine, and saliva are leading a new phase of biomarkers. Here, we reviewed these current potential diagnostic biomarkers of ALS.
肌萎缩性脊髓侧索硬化症(ALS)目前缺乏有用的诊断生物标志物。目前对肌萎缩侧索硬化症的诊断主要依赖于临床表现,这导致了诊断的延迟,难以在肌萎缩侧索硬化症早期做出准确诊断,阻碍了临床早期治疗。近 30 年来,越来越多的 ALS 发病机制被发现,包括兴奋毒性、氧化应激、线粒体功能障碍、神经炎症、能量代谢改变、RNA 错误处理以及最新的神经影像学发现。这些发病机制的发现为寻找 ALS 的诊断生物标志物提供了新的线索。目前,大量关于诊断生物标志物的相关研究正在进行中。与诊断生物标志物相关的 ALS 发病机制可能会减少诊断对临床表现的依赖。其中,通过结构和功能磁共振成像获得的 ALS 患者皮质改变特征、脑脊液中神经元缺失和胶质激活的新兴蛋白质组生物标志物以及血液、血清、尿液和唾液中的潜在生物标志物正在引领生物标志物的新阶段。在此,我们回顾了目前这些潜在的 ALS 诊断生物标志物。
期刊介绍:
Reviews in the Neurosciences provides a forum for reviews, critical evaluations and theoretical treatment of selective topics in the neurosciences. The journal is meant to provide an authoritative reference work for those interested in the structure and functions of the nervous system at all levels of analysis, including the genetic, molecular, cellular, behavioral, cognitive and clinical neurosciences. Contributions should contain a critical appraisal of specific areas and not simply a compilation of published articles.