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Discrete gait characteristics are associated with m.3243A>G and m.8344A>G variants of mitochondrial disease and its pathological consequences.
- Source :
-
Journal of neurology [J Neurol] 2014 Jan; Vol. 261 (1), pp. 73-82. Date of Electronic Publication: 2013 Oct 23. - Publication Year :
- 2014
-
Abstract
- Mitochondrial disease is complex and variable, making diagnosis and management challenging. The situation is complicated by lack of sensitive outcomes of disease severity, progression, contributing pathology and clinical efficacy. Gait is emerging as a sensitive marker of pathology; however, to date, no studies have quantified gait in mitochondrial disease. In this cross-sectional study, we quantified gait characteristics in 24 patients with genetically confirmed mitochondrial disease (m.3243A>G and m.8344A>G) and 24 controls. Gait was measured using an instrumented walkway according to a predefined model with five domains hypothesised to reflect independent features of the neural control of gait in mitochondrial disease, including: pace (step velocity and step length); rhythm (step time); variability (step length and step time variability); asymmetry (step time asymmetry); and postural stability (step width, step width variability and step length asymmetry). Gait characteristics were compared with respect to controls and genotype. Additional measures of disease severity, pathophysiology and imaging were also compared to gait to verify the validity of gait characteristics. Discrete gait characteristics differed between controls and mitochondrial disease groups, even in relatively mildly affected patients harbouring the m.3243A>G mutation. The pattern of gait impairment (increased variability and reduced postural control) was supported by significant associations with measures of disease severity, progression, pathophysiology and radiological evidence of cerebellar atrophy. Discrete gait characteristics may help describe functional deficits in mitochondrial disease, enhance measures of disease severity and pathology, and could be used to document treatment effects of novel therapies.
- Subjects :
- Adolescent
Adult
Cerebellum abnormalities
Cerebellum pathology
Cross-Sectional Studies
Female
Genotype
Humans
Male
Middle Aged
Statistics, Nonparametric
Young Adult
DNA, Mitochondrial genetics
Gait Disorders, Neurologic etiology
Mitochondrial Diseases complications
Mitochondrial Diseases genetics
Mutation genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1432-1459
- Volume :
- 261
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of neurology
- Publication Type :
- Academic Journal
- Accession number :
- 24150688
- Full Text :
- https://doi.org/10.1007/s00415-013-7129-2