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使用深度神经网络的无标记运动跟踪检测和量化啮齿动物的共济失调相关运动障碍。

Detecting and Quantifying Ataxia-Related Motor Impairments in Rodents Using Markerless Motion Tracking With Deep Neural Networks.

作者信息

Lang Jana, Haas Eva, Hubener-Schmid Jeannette, Anderson Collin J, Pulst Stefan M, Giese Martin A, Ilg Winfried

出版信息

Annu Int Conf IEEE Eng Med Biol Soc. 2020 Jul;2020:3642-3648. doi: 10.1109/EMBC44109.2020.9176701.

Abstract

In this study we evaluate the application of video-based markerless motion tracking based on deep neural networks for the analysis of ataxia-specific movement abnormalities in rodent models of cerebellar ataxia. Based on a small amount (<100) of manually labeled video frames, markerless motion tracking enabled the extraction of movement trajectories and parameters characterizing ataxia-specific movement abnormalities. In the first experiment, we analyzed videos of 6 shaker and 4 wildtype rats and were able to reproduce thê5 Hz tremor frequency in the shaker rat without the usage of a force plate. In the second experiment, we investigated a spinocerebellar ataxia type 3 (SCA3) mouse model (6 mice aged 3 months and 3 mice aged 9 months) in a beam-balancing task. By establishing a parameter for the assessment of rhythmicity of gait (RoG), we not only found a significantly higher RoG in wildtype mice compared to affected SCA3 mice aged 9 months, but were also able to reveal a significantly lower than typical RoG in SCA3 mice aged 3 months which exhibit no abnormalities in visual inspection. These prototypical results suggest the capability of the presented methods for the application in upcoming therapeutic intervention trials to identify subtle changes in movement behavior.

摘要

在本研究中,我们评估基于深度神经网络的无标记视频运动跟踪在小脑共济失调啮齿动物模型中分析共济失调特异性运动异常的应用。基于少量(<100)手动标记的视频帧,无标记运动跟踪能够提取表征共济失调特异性运动异常的运动轨迹和参数。在第一个实验中,我们分析了6只震颤大鼠和4只野生型大鼠的视频,并且在不使用测力板的情况下能够重现震颤大鼠5Hz的震颤频率。在第二个实验中,我们在横梁平衡任务中研究了3型脊髓小脑共济失调(SCA3)小鼠模型(6只3月龄小鼠和3只9月龄小鼠)。通过建立一个评估步态节律性(RoG)的参数,我们不仅发现野生型小鼠的RoG显著高于9月龄受影响的SCA3小鼠,而且还能够揭示3月龄SCA3小鼠的RoG显著低于正常水平,而这些小鼠在视觉检查中未表现出异常。这些典型结果表明所提出的方法有能力应用于即将进行的治疗干预试验,以识别运动行为中的细微变化。

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本文引用的文献

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An update on fluid biomarkers for neurodegenerative diseases: recent success and challenges ahead.
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3
Upcoming diagnostic biomarkers with promising prospects in neurological disorders.
Clin Exp Pharmacol Physiol. 2020 Mar;47(3):347-356. doi: 10.1111/1440-1681.13216. Epub 2019 Dec 21.
4
Using DeepLabCut for 3D markerless pose estimation across species and behaviors.
Nat Protoc. 2019 Jul;14(7):2152-2176. doi: 10.1038/s41596-019-0176-0. Epub 2019 Jun 21.
5
Deep cerebellar stimulation reduces ataxic motor symptoms in the shaker rat.
Ann Neurol. 2019 May;85(5):681-690. doi: 10.1002/ana.25464.
6
What have we learned recently from transgenic mouse models about neurodegeneration? The most promising discoveries of this millennium.
Pharmacol Rep. 2018 Dec;70(6):1105-1115. doi: 10.1016/j.pharep.2018.09.006. Epub 2018 Sep 16.
7
Spinocerebellar ataxias: prospects and challenges for therapy development.
Nat Rev Neurol. 2018 Oct;14(10):590-605. doi: 10.1038/s41582-018-0051-6.
8
DeepLabCut: markerless pose estimation of user-defined body parts with deep learning.
Nat Neurosci. 2018 Sep;21(9):1281-1289. doi: 10.1038/s41593-018-0209-y. Epub 2018 Aug 20.
9
Spontaneous shaker rat mutant - a new model for X-linked tremor/ataxia.
Dis Model Mech. 2016 May 1;9(5):553-62. doi: 10.1242/dmm.022848. Epub 2016 Mar 24.
10
Using the mouse to model human disease: increasing validity and reproducibility.
Dis Model Mech. 2016 Feb;9(2):101-3. doi: 10.1242/dmm.024547.

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