[HTML][HTML] Neural substrates of cognitive subtypes in Parkinson's disease: a 3-year longitudinal study

Y Shoji, Y Nishio, T Baba, M Uchiyama, K Yokoi… - PLoS …, 2014 - journals.plos.org
Y Shoji, Y Nishio, T Baba, M Uchiyama, K Yokoi, T Ishioka, Y Hosokai, K Hirayama…
PLoS One, 2014journals.plos.org
Background The neuropsychological features and neuropathological progression patterns
associated with rapidly evolving cognitive decline or dementia in Parkinson's disease (PD)
remain to be elucidated. Methods Fifty-three PD patients without dementia were recruited to
participate in a 3-year longitudinal cohort study. The patients were grouped according to the
Clinical Dementia Rating (CDR). Group-wise comparisons were made with regard to
demographic characteristics, motor symptoms, neuropsychological performances and 18F …
Background
The neuropsychological features and neuropathological progression patterns associated with rapidly evolving cognitive decline or dementia in Parkinson's disease (PD) remain to be elucidated.
Methods
Fifty-three PD patients without dementia were recruited to participate in a 3-year longitudinal cohort study. The patients were grouped according to the Clinical Dementia Rating (CDR). Group-wise comparisons were made with regard to demographic characteristics, motor symptoms, neuropsychological performances and 18F-fluorodeoxyglucose positron emission tomography.
Results
Patients who had memory-plus cognitive impairment (patients whose CDR was 0 at baseline and 0.5 in memory and other domains at follow-up, and those whose baseline CDR was 0.5 in memory and other domains) exhibited higher age at onset, visuoperceptual impairment, non-tremor-dominant motor disturbance, rapid symptomatic progression and posterior neocortical hypometabolism. In patients who were cognitively unimpaired and those who had memory-dominant cognitive impairment (patients whose CDR was 0 at baseline and 0.5 only in memory domain at follow-up, and those whose baseline CDR was 0.5 only in memory domain), the posterior neocortex was relatively unaffected until a later stage of the disease.
Conclusions
These results suggest that visuoperceptual impairment and the early involvement of the posterior neocortex may be risk factors for rapid symptomatic progression and dementia in PD.
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