Motor signs predict poor outcomes in Alzheimer disease

Neurology. 2005 May 24;64(10):1696-703. doi: 10.1212/01.WNL.0000162054.15428.E9.

Abstract

Objective: To examine whether the presence of motor signs has predictive value for important outcomes in Alzheimer disease (AD).

Methods: A total of 533 patients with AD at early stages (mean Folstein Mini-Mental State Examination [MMSE] 21/30 at entry) were recruited and followed semiannually for up to 13.1 years (mean 3) in five University-based AD centers in the United States and European Union. Four outcomes, assessed every 6 months, were used in Cox models: cognitive endpoint (Columbia Mini-Mental State Examination < or = 20/57 [ approximately MMSE < or = 10/30]), functional endpoint (Blessed Dementia Rating Scale > or = 10), institutionalization equivalent index, and death. Using a standardized portion of the Unified PD Rating Scale (administered every 6 months for a total of 3,149 visit-assessments, average 5.9 per patient), the presence of motor signs, as well as of individual motor sign domains, was examined as time-dependent predictor. The models controlled for cohort, recruitment center, sex, age, education, a comorbidity index, and baseline cognitive and functional performance.

Results: A total of 39% of the patients reached the cognitive, 41% the functional, 54% the institutionalization, and 47% the mortality endpoint. Motor signs were noted for 14% of patients at baseline and for 45% at any evaluation. Their presence was associated with increased risk for cognitive decline (RR, 1.72; 95% CI, 1.24 to 2.38), functional decline (1.80 [1.33 to 2.45]), institutionalization (1.68 [1.26 to 2.25]), and death (1.38 [1.05 to 1.82]). Tremor was associated with increased risk for reaching the cognitive and bradykinesia for reaching the functional endpoints. Postural-gait abnormalities carried increased risk for institutionalization and mortality. Faster rates of motor sign accumulation were associated with increased risk for all outcomes.

Conclusions: Motor signs predict cognitive and functional decline, institutionalization, and mortality in Alzheimer disease. Different motor sign domains predict different outcomes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / diagnosis*
  • Alzheimer Disease / mortality
  • Alzheimer Disease / physiopathology*
  • Brain / pathology
  • Brain / physiopathology*
  • Cognition Disorders / diagnosis
  • Cognition Disorders / etiology
  • Cognition Disorders / physiopathology
  • Cohort Studies
  • Disease Progression
  • Dysarthria / diagnosis
  • Dysarthria / etiology
  • Dysarthria / physiopathology
  • Female
  • Follow-Up Studies
  • Gait Disorders, Neurologic / diagnosis
  • Gait Disorders, Neurologic / etiology
  • Gait Disorders, Neurologic / physiopathology
  • Humans
  • Hypokinesia / diagnosis
  • Hypokinesia / etiology
  • Hypokinesia / physiopathology
  • Male
  • Middle Aged
  • Movement Disorders / diagnosis*
  • Movement Disorders / etiology
  • Movement Disorders / physiopathology*
  • Muscle Rigidity / diagnosis
  • Muscle Rigidity / etiology
  • Muscle Rigidity / physiopathology
  • Neurologic Examination
  • Neuropsychological Tests
  • Predictive Value of Tests
  • Prognosis
  • Proportional Hazards Models