Wearable sensors detect impaired gait and coordination in LBSL during remote assessments. Issue 4 (8th March 2022)

• Record Type: Journal Article
• Authors: Smith Fine, Amena; Kaufman, Miriam; Goodman, Jordan; Turk, Bela; Bastian, Amy; Lin, Doris; Fatemi, Ali; Keller, Jennifer
• Is Part Of: Annals of clinical and translational neurology. Volume 9:Issue 4(2022)
• Page Start: 468
• Page End: 477
• Publication Date: 2022-03-08
• Subjects: Nervous system -- Diseases -- Periodicals; Neurology -- Periodicals; 616.8005
• DOI: 10.1002/acn3.51509
• Languages: English
• ISSNs: 2328-9503

Abstract

Abstract: Background: Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) is a rare leukodystrophy with motor impairment due to biallelic mutations in DARS2, which encodes mitochondrial aspartyl tRNA synthetase. Progressive ataxia is the primary feature. Objective: The study objective is to determine the feasibility of remotely collecting quantitative gait and balance measures in LBSL. Methods: The study design uses wearable accelerometers and the scale for the assessment and rating of ataxia (SARA) scale to assess gait and postural sway in LBSL and control participants' homes through video conferencing. Results: Lateral step variability (LSV), which indicates stride variability, and elevation of the step at mid‐swing are increased for LBSL patients during brief walking tests. During stance with the eyes closed, LBSL participants show rapid accelerations and decelerations of body movement covering a large sway area and path. Both the LSV and sway area during stance with the feet together and eyes closed correlate strongly with the SARA. Conclusions: Wearable accelerometers are valid and sensitive for detecting ataxia in LBSL patients during remote assessments. The finding of large increases in the sway area during stance with the eyes closed is intriguing since dorsal column dysfunction is universally seen in LBSL. This approach can be applied to related rare diseases that feature ataxia.