The 2022 yearbook of Neurorestoratology

IF 3.1 4区 医学 Q2 CLINICAL NEUROLOGY
Hongyun Huang , John R. Bach , Hari Shanker Sharma , Hooshang Saberi , Sang Ryong Jeon , Xiaoling Guo , Ashok Shetty , Ziad Hawamdeh , Alok Sharma , Klaus von Wild , Dario Siniscalco , Paul R. Sanberg , Yong Hu , Mengzhou Xue , Lin Chen , Fabin Han , Ali Otom , Jianzhong Hu , Qiqing Zhang
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引用次数: 4

Abstract

There was much progress in the field of Neurorestoratology in the year of 2022. It included highlighting advances in understanding the pathogenesis of neurological diseases, neurorestorative mechanisms, and clinical treatments as compiled in the 2022 yearbook of Neurorestoratology. There is still controversy about whether amyloid β-protein and tau protein deposition are the reasons for or the results of Alzheimer's disease (AD) pathology. The fabricated images in important key articles that speculated on the reasons for AD pathogenesis were found. Cholinergic deficiency and decrease or loss in strength of glutamatergic synapse, limited or failing bidirectional cholinergic upregulation in early cognitive impairment, or progressive posterior-to-anterior cortical cholinergic denervation could result in the appearance of AD. Exploration of neurorestorative mechanisms were found in more detail ways in neuromodulation, immunomodulation, neurogenesis, neural network or circuitry reconstruction, neuroprotection, nervous structural repair, and neuroplasticity. Several kinds of cell therapies for neurological diseases showed neurorestorative effects in open-label and/or non-randomized clinical studies or trials. However, mesenchymal stromal cells and mononuclear cells did not demonstrate neurorestorative effects or improve the quality of life for patients with neurodegenerative diseases or neurotrauma including stroke, spinal cord injury (SCI), and amyotrophic lateral sclerosis in randomized, double-blind, placebo-controlled clinical trials (RDPCTs). Clinical treatments through neurostimulation/neuromodulation and the brain–computer/machine interface yielded positive results in AD, Parkinson's disease, stroke, SCI, cerebral palsy, and other diseases in RDPCTs. Neurorestorative surgery, pharmaceutical neurorestorative therapy and other interventions have demonstrated neurorestorative effects for various considered incurable neurological diseases in RDPCTs. Thus, this year, additional guidelines, assessment scales, and standards were set up or revised. These included guidelines of clinical neurorestorative treatments for brain trauma (2022 China version), clinical cell therapy guidelines for neurorestoration (IANR/CANR 2022), SCI or dysfunction quality of life rating scale (SCIDQLRS) (IANR 2022 version). Neurorestorative effects of varying therapeutic strategies with higher standards of evidence-based medicine are now benefiting patients with currently incurable neurological diseases. Hopefully some of them may become routine therapeutic interventions for patients with these diseases in the near future.

2022年神经修复学年鉴
2022年,神经修复学领域取得了很大进展。它包括强调在理解神经疾病的发病机制、神经修复机制和临床治疗方面的进展,这些进展被汇编在2022年的《神经修复学年鉴》中。关于淀粉样蛋白β和tau蛋白沉积是否是阿尔茨海默病(AD)病理的原因或结果,仍存在争议。在推测AD发病原因的重要关键文章中发现了伪造的图像。胆碱能缺乏和谷氨酸能突触强度降低或丧失,早期认知障碍中双向胆碱能上调受限或失败,或进行性后-前-前皮质胆碱能去神经可能导致AD的出现。在神经调控、免疫调节、,神经发生、神经网络或电路重建、神经保护、神经结构修复和神经可塑性。神经系统疾病的几种细胞疗法在开放标签和/或非随机临床研究或试验中显示出神经恢复作用。然而,在随机、双盲、安慰剂对照临床试验(RDPCT)中,间充质基质细胞和单核细胞并没有显示出神经修复作用,也没有改善神经退行性疾病或神经创伤患者的生活质量,包括中风、脊髓损伤(SCI)和肌萎缩侧索硬化症。通过神经刺激/神经调控和脑-机/机接口进行的临床治疗在AD、帕金森病、中风、SCI、脑瘫和其他RDPCT疾病中产生了积极的结果。神经修复手术、药物神经修复治疗和其他干预措施已证明对RDPCT中各种被认为无法治愈的神经疾病具有神经修复作用。因此,今年制定或修订了额外的指导方针、评估量表和标准。其中包括脑创伤临床神经修复治疗指南(2022中国版)、神经修复临床细胞治疗指南(IANR/CANR 2022)、SCI或功能障碍生活质量评定量表(SCIDQLRS)(IANR 2022版)。不同的治疗策略和更高标准的循证医学的神经恢复效果现在使目前无法治愈的神经疾病患者受益。希望在不久的将来,其中一些可以成为这些疾病患者的常规治疗干预措施。
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
Journal of Neurorestoratology
Journal of Neurorestoratology CLINICAL NEUROLOGY-
CiteScore
2.10
自引率
18.20%
发文量
22
审稿时长
12 weeks
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