4.6 Article

Postural instability/gait disturbance in Parkinson's disease has distinct subtypes: an exploratory analysis

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出版社

B M J PUBLISHING GROUP
DOI: 10.1136/jnnp.2010.222042

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资金

  1. Michael J Fox Foundation
  2. Close to a Cure Foundation
  3. NIH, Washington, DC USA [R01-NS36960]
  4. Department of Veterans Affairs
  5. New York State Department of Health Wadsworth Center, Albany, NY, USA
  6. Sartain Lanier Family Foundation, Atlanta, GA, USA
  7. TEVA Neurosciences
  8. Ipsen
  9. Schering Plough
  10. TEVA-speakers bureau
  11. Allergan
  12. Merz
  13. Boehringer-Ingelheim-speakers bureau

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Objective To test the hypothesis that postural instability with falling (PIF) and freezing of gait (FOG) are distinct subtypes of the postural instability/gait disturbance (PIGD) form of Parkinson's disease (PD). Methods 499 PD subjects from the NeuroGenetics Research Consortium were studied using logistic regression to examine, in a cross sectional analysis, predictors of FOG and PIF. Potential predictors were from four spheres; demographic, clinical motor, clinical non-motor and genetic. Results FOG and PIF were both associated with greater gait subscores and lower tremor subscores on the Unified Parkinson's Disease Rating Scale (p <= 0.02). However, they differed with regard to demographic, non-motor and genetic predictors. FOG was associated with greater duration of disease, with ORs of 3.01 (95% CI 1.35 to 6.72) and 4.91 (95% CI 2.29 to 10.54) for third and fourth quartiles of duration, respectively, versus the lowest half of duration. The risk of having psychotic symptoms was also significantly increased (OR 3.02, 95% CI 1.41 to 6.49; p=0.004). FOG was inversely associated with the presence of the CYP2D6*4 allele (OR 0.41, 95% CI 0.21 to 0.80; p=0.009) suggesting a protective effect. PIF was associated with depression (OR 1.08, 95% CI 1.01 to 1.15; p<0.02) and was inversely associated with APOE 34 (OR 0.21, 95% CI 0.05 to 0.87; p=0.03), again suggesting a protective effect. Conclusion FOG and PIF have different demographic, non-motor and genetic predictors suggesting that they may be pathophysiologically distinct subtypes of PIGD. These findings have implications in the discovery of therapeutic targets for these disabling features as well as for predicting outcomes of PD.

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