Literature DB >> 19797696

Diffusion tensor imaging, white matter lesions, the corpus callosum, and gait in the elderly.

Refeeque A Bhadelia1, Lori Lyn Price, Kurtis L Tedesco, Tammy Scott, Wei Qiao Qiu, Samuel Patz, Marshal Folstein, Irwin Rosenberg, Louis R Caplan, Peter Bergethon.   

Abstract

BACKGROUND AND
PURPOSE: Gait impairment is common in the elderly, especially those with stroke and white matter hyperintensities on conventional brain MRI. Diffusion tensor imaging (DTI) is more sensitive to white matter damage than conventional MRI. The relationship between DTI measures and gait has not been previously evaluated. Our purpose was to investigate the relationship between the integrity of white matter in the corpus callosum as determined by DTI and quantitative measures of gait in the elderly.
METHODS: One hundred seventy-three participants of a community-dwelling elderly cohort had neurological and neuropsychological examinations and brain MRI. Gait function was measured by Tinetti gait (0 to 12), balance (0 to 16) and total (0 to 28) scores. DTI assessed fractional anisotropy in the genu and splenium of the corpus callosum. Conventional MRI was used to evaluate for brain infarcts and white matter hyperintensity volume.
RESULTS: Participants with abnormal gait had low fractional anisotropy in the genu of the corpus callosum but not the splenium. Multiple regressions analyses showed an independent association between these genu abnormalities and all 3 Tinetti scores (P<0.001). This association remained significant after adding MRI infarcts and white matter hyperintensity volume to the analysis.
CONCLUSIONS: The independent association between quantitative measures of gait function and DTI findings shows that white matter integrity in the genu of corpus callosum is an important marker of gait in the elderly. DTI analyses of white matter tracts in the brain and spinal cord may improve knowledge about the pathophysiology of gait impairment and help target clinical interventions.

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Year:  2009        PMID: 19797696      PMCID: PMC3401013          DOI: 10.1161/STROKEAHA.109.564765

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


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