Literature DB >> 26578460

Effects of white matter lesions on trunk stability during dual-task walking among older adults with mild cognitive impairment.

Takehiko Doi1,2, Hiroyuki Shimada3, Hyuma Makizako4, Kota Tsutsumimoto4, Ryo Hotta4, Sho Nakakubo4, Takao Suzuki5,6.   

Abstract

The linkage between gait and cognition has been shown in cases of white matter lesion (WML) that affect gait in older adults. Dual-task walking is believed to be cognitively demanding and to alter trunk movement, and gait impairment in people with mild cognitive impairment (MCI) is highlighted under this condition. However, the association between dual-task walking and structural changes in the brain, particularly with WML, in people with MCI is still unclear. The aim of this study was to examine the association between trunk stability during dual-task walking and WML in 560 older adults with MCI. We measured magnetic resonance imaging (MRI) and gait variables. Gait variables included harmonic ratio in vertical, mediolateral, and anteroposterior directions, analyzed using a tri-axial accelerometer attached to the lower trunk. Walking conditions were normal walking and dual-task walking (counting backwards while walking) conditions. Demographical data and brain atrophy were measured as covariates. Subjects were classified into non-severe WML (n = 451, mean age = 73.2 years) and severe WML (n = 109, mean age = 75.9 years) groups. Linear mixed-effects model analysis controlled for covariates showed dual-task-related changes in all harmonic ratios associated with WML (p < 0.05). Even after adjustment for executive function, harmonic ratio in the mediolateral direction was significantly associated with WML (p < 0.05). Our findings revealed that WMLs were associated with trunk stability in dual-task walking. Further studies are required to investigate the neural basis for deficits in gait ability among MCI subjects.

Entities:  

Keywords:  Balance; Brain; Gait; MCI; MRI

Mesh:

Year:  2015        PMID: 26578460      PMCID: PMC5005854          DOI: 10.1007/s11357-015-9858-x

Source DB:  PubMed          Journal:  Age (Dordr)        ISSN: 0161-9152


  49 in total

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