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Gait Variability to Phenotype Common Orthopedic Gait Impairments Using Wearable Sensors. | LitMetric

AI Article Synopsis

  • This study investigates how gait features, measured using foot-mounted sensors during a 6-minute walk test, can differentiate between mobility impairments caused by lumbar spinal stenosis (LSS) and knee osteoarthritis (KOA).
  • Eleven gait parameters across four areas (pace, rhythm, asymmetry, variability) were analyzed, revealing that while both disease groups differed from healthy controls, they showed no significant distinctions from each other.
  • Notably, increased stride length variability emerged as a key marker to differentiate the diseases, particularly in the test's middle section, suggesting that this time frame may help identify subtle gait variations linked to different underlying conditions.

Article Abstract

Mobility impairments are a common symptom of age-related degenerative diseases. Gait features can discriminate those with mobility disorders from healthy individuals, yet phenotyping specific pathologies remains challenging. This study aims to identify if gait parameters derived from two foot-mounted inertial measurement units (IMU) during the 6 min walk test (6MWT) can phenotype mobility impairment from different pathologies (Lumbar spinal stenosis (LSS)-neurogenic diseases, and knee osteoarthritis (KOA)-structural joint disease). Bilateral foot-mounted IMU data during the 6MWT were collected from patients with LSS and KOA and matched healthy controls (N = 30, 10 for each group). Eleven gait parameters representing four domains (pace, rhythm, asymmetry, variability) were derived for each minute of the 6MWT. In the entire 6MWT, gait parameters in all four domains distinguished between controls and both disease groups; however, the disease groups demonstrated no statistical differences, with a trend toward higher stride length variability in the LSS group ( = 0.057). Additional minute-by-minute comparisons identified stride length variability as a statistically significant marker between disease groups during the middle portion of 6WMT (3rd min: ≤ 0.05; 4th min: 0.06). These findings demonstrate that gait variability measures are a potential biomarker to phenotype mobility impairment from different pathologies. Increased gait variability indicates loss of gait rhythmicity, a common feature in neurologic impairment of locomotor control, thus reflecting the underlying mechanism for the gait impairment in LSS. Findings from this work also identify the middle portion of the 6MWT as a potential window to detect subtle gait differences between individuals with different origins of gait impairment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9739785PMC
http://dx.doi.org/10.3390/s22239301DOI Listing

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