Locomotion and eye behaviour under controlled environment in individuals with Alzheimer's disease

被引:0
作者
Suzuki, Tatsuto [1 ]
Yong, Keir [2 ]
Yang, Biao [1 ]
Carton, Amelia [2 ]
McCarthy, Ian [1 ]
Papadosifos, Nikolaos [1 ]
Boampong, Derrick [1 ]
Holloway, Catherine [1 ]
Tyler, Nick [1 ]
Crutch, Sebastian [2 ]
机构
[1] UCL, Dept Civil Environm & Geomat Enginnering, Gower St, London WC1E 6BT, England
[2] UCL, Inst Neurol, Dementia Res Ctr, London WC1N 3AR, England
来源
2015 37TH ANNUAL INTERNATIONAL CONFERENCE OF THE IEEE ENGINEERING IN MEDICINE AND BIOLOGY SOCIETY (EMBC) | 2015年
基金
英国工程与自然科学研究理事会; 英国医学研究理事会;
关键词
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This study aimed to examine simple locomotion and eye behaviour of individuals with Posterior Cortical Atrophy (PCA) and typical Alzheimer's disease (tAD) within a simulated real-world environment. Posterior cortical atrophy (PCA) is a neurodegenerative condition characterised by parietal, occipital and occipito-temporal tissue loss and progressive impairment of higher-order visual function in contrast to relatively spared memory and language. Targeted types of locomotion were walking in a series of corridors, up or down stairs, and across an open room with or without the presence of an obstacle. Eye tracking measures and inertial moment units (IMU) were used in this experiment, and resultant acceleration of left foot and fixation duration were extracted. Findings from three participants are presented as a case series: one control, one PCA and one tAD patient. The averaged resultant acceleration of PCA patient was the slowest in all types of locomotion, especially in stairs. The averaged resultant accelerations of PCA and tAD participants were slower than the control participant. The PCA participant had longer mean fixation durations than the tAD and control participants, however, mean fixation duration was similar between tAD and control participants. Results may help characterise locomotion and eye behaviour in PCA and tAD and may suggest ways to support effective diagnosis and assessment of disease progression.
引用
收藏
页码:6594 / 6597
页数:4
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