Current potential diagnostic biomarkers of amyotrophic lateral sclerosis

Author:

Xu Zheqi123ORCID,Xu Renshi123ORCID

Affiliation:

1. Department of Neurology , Jiangxi Provincial People’s Hospital, The First Affiliated Hospital of Nanchang Medical College , Nanchang 330006 , China

2. The Clinical College of Nanchang Medical College , Nanchang 330006 , China

3. Medical College of Nanchang University , Nanchang 330006 , China

Abstract

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.

Funder

Jiangxi Provincial Department of Science and Technology

National Natural Science Foundation of China

Health and Family Planning Commission of Jiangxi Province

Education Department of Jiangxi Province

Publisher

Walter de Gruyter GmbH

Reference106 articles.

1. Åberg, M., Nyberg, J., Robertson, J., Kuhn, G., Schiöler, L., Nissbrandt, H., Waern, M., and Torén, K. (2018). Risk factors in Swedish young men for amyotrophic lateral sclerosis in adulthood. J. Neurol. 265: 460–470, https://doi.org/10.1007/s00415-017-8719-1.

2. Abu-Rumeileh, S., Vacchiano, V., Zenesini, C., Polischi, B., de Pasqua, S., Fileccia, E., Mammana, A., Di Stasi, V., Capellari, S., Salvi, F., et al.. (2020). Diagnostic-prognostic value and electrophysiological correlates of CSF biomarkers of neurodegeneration and neuroinflammation in amyotrophic lateral sclerosis. J. Neurol. 267: 1699–1708, https://doi.org/10.1007/s00415-020-09761-z.

3. Agosta, F., Spinelli, E.G., Marjanovic, I.V., Stevic, Z., Pagani, E., Valsasina, P., Salak-Djokic, B., Jankovic, M., Lavrnic, D., Kostic, V.S., et al.. (2018). Unraveling ALS due to SOD1 mutation through the combination of brain and cervical cord MRI. Neurology 90: e707–e716, https://doi.org/10.1212/wnl.0000000000005002.

4. Ahmed, R. and Farooqi, I.S. (2017). Hypothalamic atrophy is related to body mass index and age at onset in amyotrophic lateral sclerosis. J. Neurol. Neurosurg. Psychiatry 88: 1006–1007, https://doi.org/10.1136/jnnp-2017-316382.

5. Alruwaili, A.R., Pannek, K., Coulthard, A., Henderson, R., Kurniawan, N.D., and McCombe, P. (2018). A combined tract-based spatial statistics and voxel-based morphometry study of the first MRI scan after diagnosis of amyotrophic lateral sclerosis with subgroup analysis. J. Neuroradiol. 45: 41–48, https://doi.org/10.1016/j.neurad.2017.03.007.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3