Blume Josefine, Beniaminov Stanislav, Kämpe Björkvall Cecilia, Machaczka Maciej, Svenningsson Per
Section of Neurology, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.
Hematology Center Karolinska, Department of Medicine at Huddinge, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Front Neurol. 2017 Jun 22;8:295. doi: 10.3389/fneur.2017.00295. eCollection 2017.
Chronic neuronopathic Gaucher's disease type 3 (GD3) is relatively frequent in northern Sweden. Besides multiple other neurological symptoms, horizontal gaze palsy or oculomotor apraxia is common in GD3.
To characterize the saccades in patients with Norrbottnian GD3 with respect to their neurological and cognitive status using a computer-based eye-tracking technique.
Horizontal and vertical reflexive saccades as well as antisaccades of nine GD3 patients [4M/5F; 41.1 ± 11.0 years; modified severity scoring tool (mSST): 9.3 ± 5.4; Montreal Cognitive Assessment (MoCA): 24.0 ± 4.2] and age-matched controls were analyzed using EyeBrain T2, a head-mounted binocular eye tracker. Systematic clinical assessment included the mSST, a valid tool for monitoring the neurological progression in GD3 and MoCA.
In Norrbottnian GD3 patients, gain, peak, and average velocity (107.5°/s ± 41.8 vs. 283.9°/s ± 17.0; = 0.0009) of horizontal saccades were reduced compared to healthy controls (HCs). Regarding vertical saccades, only the average velocity of downward saccades was decreased (128.6°/s ± 63.4 vs. 244.1°/s ± 50.8; = 0.004). Vertical and horizontal saccadic latencies were increased (294.3 ms ± 37.0 vs. 236.5 ms ± 22.4; = 0.005) and the latency of horizontal reflexive saccades was correlated with the mSST score ( = 0.80; = 0.003). The latency of antisaccades showed association to MoCA score ( = 0.70; = 0.009). GD3 patients made more errors in the antisaccade task (41.5 ± 27.6% vs. 5.2 ± 5.8%; = 0.005), and the error rate tended to correlate with the cognitive function measured in MoCA score ( = 0.06).
The mean age of 41 years of our GD3 cohort reflects the increased life expectancy of patients in the Norrbottnian area compared to other GD3 cohorts. Marked impairment of horizontal saccades was evident in all patients, whereas vertical saccades showed distinct impairment of downward velocity. Latency of reflexive saccades was associated with the severity of neurological symptoms. Increased latency and error rate in the antisaccade task were linked to cognitive impairment. The assessment of saccades provides markers for neurological and neuropsychological involvement in Norrbottnian GD3.
慢性神经元型戈谢病3型(GD3)在瑞典北部相对常见。除了多种其他神经症状外,水平凝视麻痹或眼球运动失用在GD3中很常见。
使用基于计算机的眼动追踪技术,根据神经和认知状态对诺尔伯特尼亚型GD3患者的扫视运动进行特征描述。
使用头戴式双眼眼动追踪仪EyeBrain T2分析9例GD3患者[4例男性/5例女性;41.1±11.0岁;改良严重程度评分工具(mSST):9.3±5.4;蒙特利尔认知评估量表(MoCA):24.0±4.2]和年龄匹配对照的水平和垂直反射性扫视以及反扫视。系统的临床评估包括mSST,这是一种监测GD3神经进展的有效工具和MoCA。
与健康对照(HCs)相比,诺尔伯特尼亚型GD3患者水平扫视的增益、峰值和平均速度(107.5°/秒±41.8 vs. 283.9°/秒±17.0;P = 0.0009)降低。关于垂直扫视,仅向下扫视的平均速度降低(128.6°/秒±63.4 vs. 244.1°/秒±50.8;P = 0.004)。垂直和水平扫视潜伏期增加(294.3毫秒±37.0 vs. 236.5毫秒±22.4;P = 0.005),水平反射性扫视潜伏期与mSST评分相关(r = 0.80;P = 0.003)。反扫视潜伏期与MoCA评分相关(r = 0.70;P = 0.009)。GD3患者在反扫视任务中犯的错误更多(41.5±27.6% vs. 5.2±5.8%;P = 0.005),错误率倾向于与MoCA评分中测量的认知功能相关(r = 0.06)。
我们的GD3队列的平均年龄为41岁,反映了与其他GD3队列相比,诺尔伯特尼亚地区患者预期寿命的增加。所有患者均明显存在水平扫视功能障碍,而垂直扫视则表现为向下速度明显受损。反射性扫视潜伏期与神经症状的严重程度相关。反扫视任务中潜伏期增加和错误率增加与认知障碍有关。扫视运动评估为诺尔伯特尼亚型GD3的神经和神经心理受累提供了标志物。