LRRK2 and Other Novel Exosome Proteins in Parkinson's Disease
Status: | Completed |
---|---|
Conditions: | Parkinsons Disease |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 21 - Any |
Updated: | 5/13/2018 |
Start Date: | January 2013 |
End Date: | June 21, 2016 |
This proposal seeks to 1) determine whether there are biomarkers associated with Parkinson's
disease (PD) susceptibility and/or progression in exosome-proteomes derived from PD patients
versus controls, and 2) to determine if LRRK2 expression and/or phosphorylation are
significantly lowered in the exosomes of individuals treated with the potent LRRK2 kinase
inhibitor sunitinib (a multi-kinase inhibitor compound), to establish an assay for on-target
effects for future LRRK2 inhibitor clinical trials.
disease (PD) susceptibility and/or progression in exosome-proteomes derived from PD patients
versus controls, and 2) to determine if LRRK2 expression and/or phosphorylation are
significantly lowered in the exosomes of individuals treated with the potent LRRK2 kinase
inhibitor sunitinib (a multi-kinase inhibitor compound), to establish an assay for on-target
effects for future LRRK2 inhibitor clinical trials.
Inclusion Criteria:
Parkinson's disease inclusion criteria:
Inclusion criteria will be based on UK Brain Bank criteria for the clinical diagnosis of
PD. These require 1) the presence of bradykinesia and either rest tremor or rigidity; 2)
asymmetric onset; 3) progressive motor symptoms 4) age at onset 21-99 years.
Control inclusion criteria: ages of between 21-99 years, a lack of PD in first-degree blood
relatives, and a lack of positive responses on more than 3 items on the PD Screening
Questionnaire.
Exclusion Criteria:
For all subjects:
include atypical features indicative of a Parkinson-Plus disorder (Progressive Supranuclear
Palsy (PSP), Multiple System Atrophy (MSA), Corticobasal Degeneration (CBD)) including
cerebellar signs, supranuclear gaze palsy, apraxia and other cortical signs, or prominent
autonomic failure, neuroleptic treatment at time of onset of parkinsonism, active treatment
with a neuroleptic at time of study entry, History of repeated strokes with stepwise
progression of parkinsonism, history of repeated head injury, history of definite
encephalitis, prominent gait imbalance early in the course (< 5 years), dementia, known
severe anemia (hematocrit <30), history of kidney disease and/or current or past glomerular
filtration rate (GFR) <60 possibly indicative of kidney disease, or a serious comorbidity
that may interfere with participation in the study.
We found this trial at
1
site
Birmingham, Alabama 35294
Principal Investigator: Andrew West, PhD
Phone: 205-996-7697
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