Quantitative assessment of oculomotor function by videonystagmography in multiple system atrophy

被引:7
|
作者
Zhou, Hong [1 ,2 ]
Sun, Yunchuang [1 ,3 ]
Wei, Luhua [1 ,3 ]
Wang, Xia [1 ,3 ]
Jiang, Yanyan [1 ]
Li, Fan [1 ,3 ]
Chen, Jing [1 ,3 ]
Sun, Wei [1 ,3 ]
Zhang, Lin [4 ]
Zhao, Guiping [1 ,3 ,5 ]
Wang, Zhaoxia [1 ,3 ,5 ]
机构
[1] Peking Univ First Hosp, Dept Neurol, Beijing 100034, Peoples R China
[2] Civil Aviat Gen Hosp, Dept Neurol, Beijing 100123, Peoples R China
[3] Beijing Key Lab Neurovasc Dis Discovery, Beijing 100034, Peoples R China
[4] Univ Calif Davis, Dept Neurol, Med Ctr, Sacramento, CA USA
[5] Peking Univ First Hosp, Dept Neurol, 8 Xishiku St, Beijing 100034, Peoples R China
关键词
Multiple system atrophy; Oculomotor deficits; Saccades; Smooth pursuit movement; Square -wave jerks; Videonystagmography; CONSENSUS STATEMENT; PARKINSONS-DISEASE; DIAGNOSIS; SACCADE;
D O I
10.1016/j.clinph.2022.05.019
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To quantitatively assess oculomotor impairments in multiple system atrophy (MSA) and to explore their correlation with clinical characteristics. Methods: We recruited 45 patients with MSA, including 21 with dominant ataxia (MSA-C), 24 with dominant parkinsonism (MSA-P), and 40 age-matched healthy controls. Detailed oculomotor performance in the horizontal direction was measured using videonystagmography (VNG). Results: We found that the proportion of abnormal eye movements in patients with MSA was 93.3% (37.7%, 51.1%, 73.3%, 71.1%, and 37.8% on fixation and gaze-holding, without fixation, saccade, smooth pursuit, and optokinetic nystagmus tests, respectively). Patients with MSA-C showed significantly lower gains in smooth pursuit test and optokinetic nystagmus test, and a higher incidence of hypermetria in the saccade test than patients with MSA-P (all P < 0.05). No oculomotor deficits were correlated with age, age of onset, sex, disease duration, or Unified Multiple System Atrophy Rating Scale (USMARS) (all r < 0.25, P > 0.1). Conclusions: An extremely high incidence of oculomotor impairments could be observed using VNG in both the MSA-C and MSA-P subtypes, although there were some differences between them. Significance: A comprehensive oculomotor examination could serve as a valuable tool in the diagnostic workup of patients with MSA. (c) 2022 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:15 / 23
页数:9
相关论文
共 50 条
  • [21] Cognition in multiple system atrophy: neuropsychological profile and interaction with mood
    Balas, Meirav
    Balash, Yacov
    Giladi, Nir
    Gurevich, Tanya
    JOURNAL OF NEURAL TRANSMISSION, 2010, 117 (03) : 369 - 375
  • [22] Nonmotor presentations of multiple system atrophy
    Colosimo, Carlo
    NATURE REVIEWS NEUROLOGY, 2011, 7 (05) : 295 - 298
  • [23] Glutathione Depletion and MicroRNA Dysregulation in Multiple System Atrophy: A Review
    Kinoshita, Chisato
    Kubota, Noriko
    Aoyama, Koji
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (23)
  • [24] Freezing of Gait in Multiple System Atrophy
    Yang, Huaguang
    Liu, Weiyin Vivian
    Wang, Shanshan
    Yang, Wenbin
    Liu, Changsheng
    Wen, Zhi
    Hu, Lanhua
    Guo, Jinxia
    Fan, Guoguang
    Luo, Xiaoguang
    Zha, Yunfei
    FRONTIERS IN AGING NEUROSCIENCE, 2022, 14
  • [25] The Cognitive Profile and Executive Function of Progressive Supranuclear Palsy and Multiple System Atrophy Patients
    Goel, Divya
    Vyas, Arvind
    INDIAN JOURNAL OF MEDICAL SPECIALITIES, 2019, 10 (02) : 84 - 88
  • [26] Prospective CERAD Neuropsychological Assessment in Patients With Multiple System Atrophy
    Maass, Fabian
    Hermann, Peter
    Varges, Daniela
    Nuhn, Sabine
    van Riesen, Christoph
    Jamous, Ala
    Focke, Niels K.
    Hewitt, Manuel
    Leha, Andreas
    Baehr, Mathias
    Zerr, Inga
    FRONTIERS IN NEUROLOGY, 2022, 13
  • [27] Anorectal function in multiple system atrophy and Parkinson's disease
    Stocchi, F
    Badiali, D
    Vacca, L
    D'Alba, L
    Bracci, F
    Ruggieri, S
    Torti, M
    Berardelli, A
    Corazziari, E
    MOVEMENT DISORDERS, 2000, 15 (01) : 71 - 76
  • [28] Epidemiology of Multiple System Atrophy in Hokkaido, the Northernmost Island of Japan
    Sakushima, Ken
    Nishimoto, Naoki
    Nojima, Masanori
    Matsushima, Masaaki
    Yabe, Ichiro
    Sato, Norihiro
    Mori, Mitsuru
    Sasaki, Hidenao
    CEREBELLUM, 2015, 14 (06) : 682 - 687
  • [29] The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy
    Wenning, Gregor K.
    Stankovic, Iva
    Vignatelli, Luca
    Fanciulli, Alessandra
    Calandra-Buonaura, Giovanna
    Seppi, Klaus
    Palma, Jose-Alberto
    Meissner, Wassilios G.
    Krismer, Florian
    Berg, Daniela
    Cortelli, Pietro
    Freeman, Roy
    Halliday, Glenda
    Hoeglinger, Gunter
    Lang, Anthony
    Ling, Helen
    Litvan, Irene
    Low, Phillip
    Miki, Yasuo
    Panicker, Jalesh
    Pellecchia, Maria Teresa
    Quinn, Niall
    Sakakibara, Ryuji
    Stamelou, Maria
    Tolosa, Eduardo
    Tsuji, Shoji
    Warner, Tom
    Poewe, Werner
    Kaufmann, Horacio
    MOVEMENT DISORDERS, 2022, 37 (06) : 1131 - 1148
  • [30] Current Treatment of Multiple System Atrophy
    Maass, Sylvia
    Levin, Johannes
    Hoeglinger, Guenter
    CURRENT TREATMENT OPTIONS IN NEUROLOGY, 2016, 18 (12)