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早期多发性硬化症中心血管自主神经调节异常与视网膜的神经退行性相互作用

Neurodegenerative Interplay of Cardiovascular Autonomic Dysregulation and the Retina in Early Multiple Sclerosis.

作者信息

de Rodez Benavent Sigrid A, Nygaard Gro O, Nilsen Kristian B, Etholm Lars, Sowa Piotr, Wendel-Haga Marte, Harbo Hanne F, Drolsum Liv, Laeng Bruno, Kerty Emilia, Celius Elisabeth G

机构信息

Department of Ophthalmology, Oslo University Hospital, Oslo, Norway.

Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

出版信息

Front Neurol. 2019 May 15;10:507. doi: 10.3389/fneur.2019.00507. eCollection 2019.

Abstract

Autonomic nervous system (ANS) symptoms are prevalent in multiple sclerosis (MS) as is neurodegeneration. Our aim was to explore the occurrence of ANS symptoms and retinal neurodegeneration in a newly diagnosed MS population with tools available in a clinical setting. Forty-three MS patients and 44 healthy controls took part in the study. We employed a bedside cardiovascular ANS test battery together with classical pupillometry, optical coherence tomography (OCT) evaluation of retinal neurodegeneration in eyes without previous optic neuritis (MSNON) and patients' self-report forms on fatigue, orthostatic and ANS symptoms. Half of the patients presented with ANS symptoms and a high level of fatigue. There was a significant difference in ganglion cell layer thickness (mean GCIPL) evaluated by OCT in MSNON compared to healthy control eyes. We found a negative linearity of mean GCIPL on group level with increasing disease duration. Three patients fulfilled the criteria of postural orthostatic tachycardia syndrome (POTS). Our results demonstrate retinal neurodegeneration in MSNON, a high frequency of fatigue and a high prevalence of ANS symptoms in newly diagnosed patients. Whether neurodegeneration precedes ANS dysfunction or vice versa is still open to debate, but as unveiled by the presence of POTS in this MS population, differences in stress-response regulation add to the understanding of variation in onset-time of ANS dysfunction in early MS.

摘要

自主神经系统(ANS)症状在多发性硬化症(MS)中普遍存在,神经退行性变也是如此。我们的目的是利用临床环境中可用的工具,探讨新诊断的MS患者群体中ANS症状和视网膜神经退行性变的发生情况。43例MS患者和44例健康对照参与了该研究。我们采用了床边心血管ANS测试组合,以及经典的瞳孔测量法、对既往无视神经炎的眼睛(MSNON)进行视网膜神经退行性变的光学相干断层扫描(OCT)评估,还有患者关于疲劳、体位性和ANS症状的自我报告表格。一半的患者出现了ANS症状和高水平的疲劳。与健康对照眼睛相比,OCT评估的MSNON患者的神经节细胞层厚度(平均GCIPL)存在显著差异。我们发现,在群体水平上,随着疾病持续时间的增加,平均GCIPL呈负线性关系。3例患者符合体位性直立性心动过速综合征(POTS)的标准。我们的结果表明,MSNON患者存在视网膜神经退行性变、高频率的疲劳以及新诊断患者中ANS症状的高患病率。神经退行性变是先于ANS功能障碍还是反之亦然仍有待讨论,但正如该MS群体中POTS的存在所揭示的那样,应激反应调节的差异有助于理解早期MS中ANS功能障碍发病时间的变化。

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