TY - JOUR
T1 - Markerless analysis of hindlimb kinematics in spinal cord-injured mice through deep learning
AU - Sato, Yuta
AU - Kondo, Takahiro
AU - Shinozaki, Munehisa
AU - Shibata, Reo
AU - Nagoshi, Narihito
AU - Ushiba, Junichi
AU - Nakamura, Masaya
AU - Okano, Hideyuki
N1 - Funding Information:
We thank Akito Kosugi and Seitaro Iwama for their technical assistance. This research was supported by AMED under grant No. JP21bm0204001h (to H.O. and M.N.), and JSPS KAKENHI Grant Nos. JP19H03983 , 19K16190 , and JP20H05480 .
Funding Information:
HO is a compensated scientific consultant of San Bio, Co., Ltd., and K Pharma, Inc., and has received research funding from Dainippon Sumitomo Pharmaceutical Co., Ltd. MN is a compensated scientific consultant at K Pharma, Inc. JU is a founder and the Representative Director of the University Startup Company, Connect Inc., for the research, development, and sale of rehabilitation devices including the brain-computer interface. He received a salary from Connect Inc. and held shares in Connect Inc. This company has no relationship with the present study. TK and YS are the founders of ALAN Inc. and held shares in ALAN Inc.
Publisher Copyright:
© 2021
PY - 2022/3
Y1 - 2022/3
N2 - Rodent models are commonly used to understand the underlying mechanisms of spinal cord injury (SCI). Kinematic analysis, an important technique to measure dysfunction of locomotion after SCI, is generally based on the capture of physical markers placed on bony landmarks. However, marker-based studies face significant experimental hurdles such as labor-intensive manual joint tracking, alteration of natural gait by markers, and skin error from soft tissue movement on the knee joint. Although the pose estimation strategy using deep neural networks can solve some of these issues, it remains unclear whether this method is adaptive to SCI mice with abnormal gait. In the present study, we developed a deep learning based markerless method of 2D kinematic analysis to automatically track joint positions. We found that a relatively small number (< 200) of manually labeled video frames was sufficient to train the network to extract trajectories. The mean test error was on average 3.43 pixels in intact mice and 3.95 pixels in SCI mice, which is comparable to the manual tracking error (3.15 pixels, less than 1 mm). Thereafter, we extracted 30 gait kinematic parameters and found that certain parameters such as step height and maximal hip joint amplitude distinguished intact and SCI locomotion.
AB - Rodent models are commonly used to understand the underlying mechanisms of spinal cord injury (SCI). Kinematic analysis, an important technique to measure dysfunction of locomotion after SCI, is generally based on the capture of physical markers placed on bony landmarks. However, marker-based studies face significant experimental hurdles such as labor-intensive manual joint tracking, alteration of natural gait by markers, and skin error from soft tissue movement on the knee joint. Although the pose estimation strategy using deep neural networks can solve some of these issues, it remains unclear whether this method is adaptive to SCI mice with abnormal gait. In the present study, we developed a deep learning based markerless method of 2D kinematic analysis to automatically track joint positions. We found that a relatively small number (< 200) of manually labeled video frames was sufficient to train the network to extract trajectories. The mean test error was on average 3.43 pixels in intact mice and 3.95 pixels in SCI mice, which is comparable to the manual tracking error (3.15 pixels, less than 1 mm). Thereafter, we extracted 30 gait kinematic parameters and found that certain parameters such as step height and maximal hip joint amplitude distinguished intact and SCI locomotion.
KW - Behavioral assessments
KW - Deep learning
KW - Kinematics
KW - Locomotion
KW - Locomotor function
KW - Spinal cord injury
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U2 - 10.1016/j.neures.2021.09.001
DO - 10.1016/j.neures.2021.09.001
M3 - Article
C2 - 34508755
AN - SCOPUS:85114986990
SN - 0168-0102
VL - 176
SP - 49
EP - 56
JO - Neuroscience Research
JF - Neuroscience Research
ER -