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Motor stereotypies in adult patients with Tourette syndrome 成年抽动秽语综合征患者的运动刻板印象
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2020-05-01 DOI: 10.2217/fnl-2019-0031
Maneeka Ubhi, K. Achinivu, S. Seri, A. Cavanna
Maneeka Ubhi1, Kanu Achinivu1, Stefano Seri2 & Andrea E Cavanna*,1,2,3 1Michael Trimble Neuropsychiatry Research Group, University of Birmingham & BSMHFT, Birmingham, UK 2School of Life & Health Sciences, Aston University, Birmingham, UK 3Sobell Department of Motor Neuroscience & Movement Disorders, Institute of Neurology & University College London, UK *Author for correspondence: a.e.cavanna@bham.ac.uk
Maneeka Ubhi1, Kanu Achinivu1, Stefano Seri2和Andrea E Cavanna*,1,2,3 1英国伯明翰大学和BSMHFT michael Trimble神经精神病学研究小组2英国伯明翰阿斯顿大学生命与健康科学学院3英国伦敦大学神经病学研究所sobell运动神经科学与运动障碍学系*通信作者:a.e.cavanna@bham.ac.uk
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引用次数: 6
Interferon beta-1a induces expression of brain-derived neurotrophic factor in human T lymphocytes in vitro and not in vivo 干扰素β-1a在体外和非体内诱导人T淋巴细胞表达脑源性神经营养因子
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2020-02-01 DOI: 10.2217/fnl-2019-0018
Zarlascht Karmand, H. Hartung, O. Neuhaus
Aim: To detect IFN β-1a-induced expression of brain-derived neurotrophic factor (BDNF) to undermine the hypothesis of IFN β-1a-associated neuroprotection in multiple sclerosis (MS). Methods: The influence of IFN β-1a on in vitro activated peripheral blood lymphocytes from healthy donors was tested. Proliferation analyses were made to detect T-cell growth. BDNF expression was measured by standard ELISA. To assess the influence of IFN β-1a on BDNF expression in vivo, BDNF serum levels of MS patients treated with IFN β-1a were compared with those of untreated patients. Results: IFN β-1a inhibited T-cell proliferation dose dependently. It induced BDNF expression at middle concentrations. MS patients treated with IFN β-1a exhibited significantly lower BDNF serum levels than untreated patients. Conclusion: IFN β-1a may promote neuroprotection by inducing BDNF expression, but its importance in vivo remains open.
目的:检测干扰素β1a诱导的脑源性神经营养因子(BDNF)的表达,以破坏干扰素β1a对多发性硬化症(MS)相关神经保护的假说。方法:检测干扰素β-1a对健康献血员体外活化的外周血淋巴细胞的影响。进行增殖分析以检测T细胞的生长。通过标准ELISA测定BDNF的表达。为了评估IFNβ-1a对体内BDNF表达的影响,将接受IFNβ-1 a治疗的MS患者和未接受治疗的患者的BDNF血清水平进行比较。结果:IFNβ-1a对T细胞增殖具有剂量依赖性抑制作用。它在中等浓度下诱导BDNF的表达。接受IFNβ-1a治疗的MS患者的BDNF血清水平明显低于未接受治疗的患者。结论:IFNβ-1a可能通过诱导BDNF表达来促进神经保护作用,但其在体内的重要性尚不明确。
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引用次数: 3
How does editing the genome improve targeting DNA and RNA for cerebellar ataxias? 编辑基因组如何改善小脑共济失调的靶向DNA和RNA?
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2020-02-01 DOI: 10.2217/fnl-2019-0019
J. Gandini, M. Manto
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引用次数: 0
Chronic stress, physiological adaptation and developmental programming of the neuroendocrine stress system 慢性应激、神经内分泌应激系统的生理适应与发育规划
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2020-02-01 DOI: 10.2217/fnl-2019-0014
J. Coffman
Chronic stress undermines physical and mental health, in part via dysregulation of the neuroendocrine stress system. Key to understand this dysregulation is recognizing that the problem is not stress per se, but rather its chronicity. The optimally functioning stress system is highly dynamic, and negative feedback regulation enforces transient responses to acute stressors. Chronic stress overrides this, and adaptation to the chronicity can result in persistent dysregulation by altering sensitivity thresholds critical for control of system dynamics. Such adaptation involves plasticity within the central nervous system (CNS) as well as epigenetic regulation. When it occurs during development, it can have persistent effects on neuroendocrine regulation. Understanding how chronic stress programs development of the neuroendocrine stress system requires elucidation of stress-responsive gene regulatory networks that control CNS plasticity and development.
慢性压力会损害身体和精神健康,部分原因是神经内分泌压力系统失调。理解这种失调的关键是认识到问题不是压力本身,而是它的长期性。最佳功能的压力系统是高度动态的,负反馈调节强制对急性压力源的短暂反应。慢性压力超越了这一点,对慢性的适应可以通过改变对系统动力学控制至关重要的敏感性阈值而导致持续的失调。这种适应涉及中枢神经系统(CNS)的可塑性以及表观遗传调节。当它发生在发育过程中,它可以对神经内分泌调节产生持久的影响。了解慢性应激如何影响神经内分泌应激系统的发展,需要阐明控制中枢神经系统可塑性和发育的应激反应基因调控网络。
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引用次数: 12
What is the role of post acute EEG in prediction of late neurological outcome in severe disorders of consciousness? 急性后脑电图在预测严重意识障碍的晚期神经系统结果中的作用是什么?
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2020-02-01 DOI: 10.2217/fnl-2019-0017
M. Scarpino, F. Lolli, G. Lanzo, A. Grippo
Causes of development of severe disorders of consciousness Hypoxic-ischemic encephalopathy, traumatic brain injury, intracerebral hemorrhage, subarachnoid hemorrhage and brain infarction are common causes of mortality and morbidity [1–8]. Many patients affected by these acquired brain injuries (ABIs) die in the acute stages during their stay in the intensive care unit; others, after a coma phase, usually develop a severe disorder of consciousness (DoC), characterized by an unresponsive wakefulness syndrome or a minimally conscious state (MCS). In some cases, consciousness level improves, transitioning to an emergence from MCS (E-MCS); however, patients with E-MCS often show a severe neurological disability [9]. In recent years, improvements both in intensive care technology and in neurosurgical procedures have reduced the mortality rate; however, as a result, many patients discharged from the acute setting exhibit severe DoCs.
严重意识障碍的发展原因缺氧缺血性脑病、创伤性脑损伤、脑出血、蛛网膜下腔出血和脑梗死是导致死亡和发病的常见原因[1-8]。许多受这些后天性脑损伤(ABI)影响的患者在重症监护室期间在急性期死亡;其他人在昏迷阶段后,通常会发展为严重的意识障碍(DoC),其特征是无反应清醒综合征或最低意识状态(MCS)。在某些情况下,意识水平提高,从MCS(E-MCS)过渡到出现;然而,E-MCS患者往往表现出严重的神经功能障碍[9]。近年来,重症监护技术和神经外科手术的改进降低了死亡率;然而,结果是,许多从急性环境中出院的患者表现出严重的DoCs。
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引用次数: 1
Welcome to the 15th volume of Future Neurology 欢迎来到《未来神经学》第15卷
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2020-02-01 DOI: 10.2217/fnl-2019-0027
Kate Lovesey
To all our readers, we are delighted to welcome you to the fifteenth volume of Future Neurology. We are also excited to welcome you to the second Open Access issue of the journal. Since the launch of this title, we have continued to publish high-quality scientific research and commentary, and the open access model will allow us to share our great content with an even bigger audience. 2019 was another exciting year for Future Neurology with the continued publication of timely, high quality manuscripts. We are proud to present some of our content highlights within this article. We would also like to take this opportunity to thank all of our valued Editorial Board members, readers and contributors for their continued support. As we move into 2020, we very much look forward to seeing the journals continuous progression and development.
对于我们所有的读者,我们很高兴欢迎你们来到《未来神经病学》第十五卷。我们也很高兴欢迎您参加该杂志的第二期开放获取。自该标题发布以来,我们一直在发布高质量的科学研究和评论,开放获取模式将使我们能够与更多的观众分享我们的精彩内容。2019年是《未来神经病学》激动人心的又一年,持续出版及时、高质量的手稿。我们很荣幸在本文中介绍我们的一些内容亮点。我们还要借此机会感谢我们所有宝贵的编委会成员、读者和撰稿人的持续支持。随着我们进入2020年,我们非常期待看到期刊的不断进步和发展。
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引用次数: 0
Strength and physical functions in people with Parkinson's disease 帕金森病患者的力量和身体功能
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2019-11-01 DOI: 10.2217/fnl-2019-0009
Sacha Clael, L. Bezerra
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引用次数: 1
Pharmacology and potential therapeutic uses of some cannabinoids 一些大麻素的药理学和潜在的治疗用途
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2019-11-01 DOI: 10.2217/fnl-2019-0010
R. Pertwee
Roger Pertwee speaks to Jennifer Straiton, Assistant Editor, at the BNA 2019 Festival of Neuroscience (14–17 April, Dublin, Ireland), where he gave a talk titled ‘Pharmacological actions and potential novel therapeutic uses of certain plant and synthetic cannabinoids’. Roger Pertwee is an Emeritus Professor at the University of Aberdeen (Scotland, UK), where he has been active in scientific research since 1974. He began his research career at the University of Oxford (UK) where he gained three postgraduate degrees: an MA in biochemistry, a DPhil in pharmacology and a DSc in physiological sciences. His research focuses on the pharmacology of cannabinoids, both on their mechanisms of action and on their potential therapeutic uses. He has held major roles in multiple major discoveries in the field including; the discovery of a cannabinoid CB1 receptor allosteric site, the pharmacological characterization of various phytocannabinoids as well as the co-discovery of endocannabinoids and the co-discovery and characterization of novel synthetic cannabinoids.
Roger Pertwee在BNA 2019神经科学节(4月14日至17日,爱尔兰都柏林)上与助理编辑Jennifer Straiton进行了交谈,他在会上发表了题为“某些植物和合成大麻素的药理作用和潜在的新治疗用途”的演讲。Roger Pertwee是阿伯丁大学(英国苏格兰)的名誉教授,自1974年以来一直活跃于该校的科学研究。他在英国牛津大学开始了他的研究生涯,在那里他获得了三个研究生学位:生物化学硕士、药理学博士和生理科学博士。他的研究重点是大麻素的药理学,包括其作用机制和潜在的治疗用途。他在该领域的多项重大发现中发挥了重要作用,包括:;大麻素CB1受体变构位点的发现,各种植物大麻素的药理学特征,以及内源性大麻素和新型合成大麻素共同发现和表征。
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引用次数: 0
Aging and eye tracking: in the quest for objective biomarkers 衰老和眼动追踪:寻找客观的生物标志物
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2019-11-01 DOI: 10.2217/fnl-2019-0012
R. Z. Marandi, P. Gazerani
Recent applications of eye tracking for diagnosis, prognosis and follow-up of therapy in age-related neurological or psychological deficits have been reviewed. The review is focused on active aging, neurodegeneration and cognitive impairments. The potential impacts and current limitations of using characterizing features of eye movements and pupillary responses (oculometrics) as objective biomarkers in the context of aging are discussed. A closer look into the findings, especially with respect to cognitive impairments, suggests that eye tracking is an invaluable technique to study hidden aspects of aging that have not been revealed using any other noninvasive tool. Future research should involve a wider variety of oculometrics, in addition to saccadic metrics and pupillary responses, including nonlinear and combinatorial features as well as blink- and fixation-related metrics to develop biomarkers to trace age-related irregularities associated with cognitive and neural deficits.
本文综述了近年来眼动追踪在年龄相关性神经或心理缺陷的诊断、预后和随访治疗中的应用。这篇综述的重点是主动衰老、神经变性和认知障碍。本文讨论了在衰老背景下使用眼动和瞳孔反应特征(眼测)作为客观生物标志物的潜在影响和当前局限性。仔细研究一下这些发现,尤其是关于认知障碍的发现,就会发现眼动追踪是一种非常宝贵的技术,可以用来研究衰老的隐藏方面,而这些方面是其他非侵入性工具无法揭示的。未来的研究应该包括更广泛的眼视测量,除了扫视测量和瞳孔反应,包括非线性和组合特征,以及眨眼和注视相关的指标,以开发生物标志物,追踪与认知和神经缺陷相关的年龄相关的不规则性。
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引用次数: 22
Seizures in cancer patients: a vast spectrum of etiologies 癌症患者的癫痫发作:广泛的病因
IF 1.3 Q4 CLINICAL NEUROLOGY Pub Date : 2019-11-01 DOI: 10.2217/fnl-2019-0015
Jad Costa, F. Haddad, G. Costa, A. Harb, R. Eid, H. Kourie, J. Helou
Aim: This study aims to recognize the distribution of different seizures etiologies in cancer patients, the most common primary tumors responsible for brain metastases, the most epileptogenic primary tumors and the therapeutic modalities. Methods: A retrospective study was conducted at Hotel-Dieu de France Hospital targeting patients admitted to hematology–oncology department between 2005 and 2016 who presented a seizure. Results: Of the 153 included patients, mean age was 57 years (standard deviation = 16 years) and a male predominance (66%). The majority of seizures were due to a primary tumor (49%) or brain metastases (32%). Other reversible (metabolic and drug) or nonreversible causes (carcinomatous meningitis, radiation and cardiovascular complications) formed the remaining causes. Regarding antiepileptic treatments, sodium valproate was mostly used, followed by levetiracetam and phenytoin. Conclusion: Numerous reversible causes are involved in the onset of epileptic seizures, including metabolic disorders, antibiotics and chemotherapies.
目的:本研究旨在了解癌症患者不同癫痫病因的分布、最常见的脑转移原发肿瘤、最常见的致痫原发肿瘤及治疗方式。方法:回顾性研究在Hotel-Dieu de France医院对2005 - 2016年在血液肿瘤科就诊的癫痫患者进行研究。结果:153例患者的平均年龄为57岁(标准差为16岁),男性占多数(66%)。大多数癫痫发作是由于原发肿瘤(49%)或脑转移(32%)。其他可逆(代谢和药物)或不可逆转的原因(癌性脑膜炎、辐射和心血管并发症)构成了剩余的原因。抗癫痫药物以丙戊酸钠为主,左乙拉西坦次之,苯妥英次之。结论:许多可逆的原因参与癫痫发作,包括代谢紊乱,抗生素和化疗。
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引用次数: 1
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Future Neurology
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