Evaluation of a Biomarker Related to the GI Tract for the Diagnosis of Parkinson's Disease
| Status: | Completed |
|---|---|
| Conditions: | Parkinsons Disease |
| Therapuetic Areas: | Neurology |
| Healthy: | No |
| Age Range: | 30 - 90 |
| Updated: | 2/7/2015 |
| Start Date: | July 2013 |
| End Date: | June 2014 |
| Contact: | Gian D Pal, MD |
| Email: | gian_d_pal@rush.edu |
| Phone: | 312-563-4772 |
Lipopolysaccharide Binding Protein as a Potential Biomarker of Parkinson's Disease
The cause of Parkinson's disease (PD) is currently unknown. Both environmental and genetic
factors have been found to contribute to PD pathogenesis. The pathology of PD is
distributed throughout the entire nervous system including the central, peripheral, and
enteric nervous system. There is evidence that inflammation plays a major role in
neurodegeneration in PD. In both the striatum and substantia nigra of PD patients activated
microglia were found and proinflammatory cytokines (TNF, IL-1B, IL-6, iNOS) are increased in
the CSF. An inflammation-driven animal model has emerged and has been widely accepted as a
model of the disease based on lipopolysaccharide (LPS) induced neurotoxicity. LPS is an
endotoxin found on the outer membrane of gram negative bacteria and humans are exposed to
LPS through the intestinal tract. The intestinal tract and thus the enteric nervous system
serve as a conduit to the central nervous system. It has been posited that the inflammatory
process could gain access to the lower brainstem via the vagal nerve and then ascend through
the basal mid- and forebrain until it reaches the cerebral cortex, producing various
pre-motor and motor symptoms of PD along the way. LPS may be one of the inflammatory
triggers involved in this process. Systemic exposure to bacterial endotoxin can be
determined by measuring plasma LPS binding protein (LBP). A study of 9 patients with early
PD (median Hoehn and Yahr stage 2) and age matched controls found that the PD subjects had a
significantly lower mean level of plasma LBP compared to control subjects. The aim of the
research plan is to establish LBP as a potential biomarker for PD across a spectrum of
disease severity.
factors have been found to contribute to PD pathogenesis. The pathology of PD is
distributed throughout the entire nervous system including the central, peripheral, and
enteric nervous system. There is evidence that inflammation plays a major role in
neurodegeneration in PD. In both the striatum and substantia nigra of PD patients activated
microglia were found and proinflammatory cytokines (TNF, IL-1B, IL-6, iNOS) are increased in
the CSF. An inflammation-driven animal model has emerged and has been widely accepted as a
model of the disease based on lipopolysaccharide (LPS) induced neurotoxicity. LPS is an
endotoxin found on the outer membrane of gram negative bacteria and humans are exposed to
LPS through the intestinal tract. The intestinal tract and thus the enteric nervous system
serve as a conduit to the central nervous system. It has been posited that the inflammatory
process could gain access to the lower brainstem via the vagal nerve and then ascend through
the basal mid- and forebrain until it reaches the cerebral cortex, producing various
pre-motor and motor symptoms of PD along the way. LPS may be one of the inflammatory
triggers involved in this process. Systemic exposure to bacterial endotoxin can be
determined by measuring plasma LPS binding protein (LBP). A study of 9 patients with early
PD (median Hoehn and Yahr stage 2) and age matched controls found that the PD subjects had a
significantly lower mean level of plasma LBP compared to control subjects. The aim of the
research plan is to establish LBP as a potential biomarker for PD across a spectrum of
disease severity.
Inclusion Criteria for Parkinson's disease subjects:
- Patients with a clinical diagnosis of Parkinson's disease by United Kingdom Parkinson
Disease Society Brain Bank criteria will be recruited.
- Hoehn and Yahr stage 1-5
- Parkinson's disease symptomatic treatment will be allowed.
Exclusion Criteria for Parkinson's disease subjects:
- Treatment with medications that may induce parkinsonism (metoclopramide, typical, or
atypical antipsychotic agents)
- Known diagnosis of inflammatory bowel disease.
- Symptomatic functional GI disease that significantly impairs intestinal mobility such
as scleroderma or use of GI motility drugs.
- Acute illness requiring immediate hospitalization.
- Presence of short bowel syndrome or severe malnutrition with ideal body weight < or =
90%
Inclusion Criteria for control subjects:
- No evidence of GI symptoms other than minor hematochezia attributable to hemorrhoids.
- No evidence of symptoms of Parkinson's disease.
- Matching in age and gender to the Parkinson's disease patients.
Exclusion Criteria for control subjects:
- Presence of Parkinson's disease or its symptoms.
- Treatment with medications that may induce parkinsonism (metoclopramide, typical, or
atypical antipsychotic agents)
- Known diagnosis of inflammatory bowel disease.
- Symptomatic functional GI disease that significantly impairs intestinal mobility such
as scleroderma or use of GI motility drugs.
- Acute illness requiring immediate hospitalization.
- Presence of short bowel syndrome or severe malnutrition with ideal body weight < or =
90%
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