Background Neurologic abnormalities affecting gait occur earlyin several types of non-Alzheimer's dementias, but their valuein predicting the development of dementia is uncertain.
Methods We analyzed the relation between neurologic gait statusat base line and the development of dementia in a prospectivestudy involving 422 subjects older than 75 years of age wholived in the community and did not have dementia at base line.Cox proportional-hazards regression analysis was used to calculatehazard ratios with adjustment for potential confounding demographic,medical, and cognitive variables.
Results At enrollment, 85 subjects had neurologic gait abnormalitiesof the following types: unsteady gait (in 31 subjects), frontalgait (in 12 subjects), hemiparetic gait (in 11 subjects), neuropathicgait (in 11 subjects), ataxic gait (in 10 subjects), parkinsoniangait (in 8 subjects), and spastic gait (in 2 subjects). Duringfollow-up (median duration, 6.6 years), there were 125 newlydiagnosed cases of dementia, 70 of them cases of Alzheimer'sdisease and 55 cases of non-Alzheimer's dementia (47 of whichinvolved vascular dementia and 8 of which involved other typesof dementia). Subjects with neurologic gait abnormalities hada greater risk of development of dementia (hazard ratio, 1.96[95 percent confidence interval, 1.30 to 2.96]). These subjectshad an increased risk of non-Alzheimer's dementia (hazard ratio,3.51 [95 percent confidence interval, 1.98 to 6.24]), but notof Alzheimer's dementia (hazard ratio, 1.07 [95 percent confidenceinterval, 0.57 to 2.02]). Of non-Alzheimer's dementias, abnormalgait predicted the development of vascular dementia (hazardratio, 3.46 [95 percent confidence interval, 1.86 to 6.42]).Among the types of abnormal gait, unsteady gait predicted vasculardementia (hazard ratio, 2.61), as did frontal gait (hazard ratio,4.32) and hemiparetic gait (hazard ratio, 13.13).
Conclusions The presence of neurologic gait abnormalities inelderly persons without dementia at base line is a significantpredictor of the risk of development of dementia, especiallynon-Alzheimer's dementia.
Source Information
From the Department of Neurology (J.V., R.B.L., C.B.H., G.K., M.J.K., H.B.) and the Department of Epidemiology and Social Medicine (R.B.L., C.B.H.), Albert Einstein College of Medicine, Bronx, N.Y.; and Innovative Medical Research and the Center for Healthier Aging (Advanced PCS), Hunt Valley, Md. (R.B.L.).
Address reprint requests to Dr. Verghese at the Einstein Aging Study, Albert Einstein College of Medicine, 1165 Morris Park Ave., Bronx, NY 10461, or at jverghes{at}aecom.yu.edu.
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