Brain · 1996 · 363 citations · 14 references
Life SciencesNeurologyNeuroscienceClinical NeuroscienceNeurodegenerationNeuroradiologyDopaminergic SignalingNeurodegenerative DiseasesNeurodegenerative DisordersParkinson DiseaseParkinsonian DisordersBiomarkers Of Parkinsonian DisordersControl Group DesignDisease Progression PredictionDisease Progression StagingMatched Control GroupParkinson Disease BiomarkersParkinson Disease ImagingUnified Parkinson's Disease Rating Scale
The study examined disease progression in 10 recent‑onset and 7 established Parkinson’s disease patients using clinical assessment and [18F]dopa‑PET, comparing results with 10 normal controls. Mean putamen [18F]dopa influx (Ki) was a reliable, highly sensitive marker of progression, declining on average 12.5% per year, with recent‑onset patients showing a faster but not statistically significant rate, and a 79 % normal Ki corresponding to symptom onset, implying a ~3.1‑year preclinical phase.
We have studied disease progression in a group of 10 patients with recent onset idiopathic Parkinson's disease [mean age 53.7±12.6 years, mean duration 18.3±6.5 months, mean unified Parkinson's disease rating scale (UPDRS) 19.0±9.5], and a group of seven patients with established Parkinson's disease (mean age 60.1±15.1 years, mean duration 70.8±35.5 months, mean UPDRS 47.9±18.1), using both clinical assessment and [18F]dopa-PET. Results were compared with those of a group of 10 normal subjects (age 66±16 years). Mean putamen [18F]dopa influx constant (K1 ) was a reliable measurement (R = 0.82) and the most sensitive marker of disease progression (r = -0.85, P < 0.0001). The mean annual rate of reduction in mean putamen Ki in the Parkinson's disease patients was 12.5% per annum, whereas the control group showed no significant change in K; over a mean of 32 months follow up. The rate of progression was more rapid in the recent onset compared with the established disease group but this did not reach statistical significance. Assuming a linear progression for the entire group we estimate symptom onset at a mean putamen K1 79% of normal with a mean preclinical period of 3.1 years.
14
Co-planar stereotaxic atlas of the human brain
Lauri A. Laitinen · Clinical Neurology and Neurosurgery · 1989 · 7.6K citations
Medicine, Anatomy, Neuroscience +12
AGEING AND PARKINSON'S DISEASE: SUBSTANTIA NIGRA REGIONAL SELECTIVITY
Julian Fearnley, Andrew J. Lees · Brain · 1991 · 3.5K citations