Evaluation of a Biomarker Related to the GI Tract for the Diagnosis 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.

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Key information

Conditions

Parkinson's Disease Basal Ganglia Diseases Brain Diseases Central Nervous System Diseases Movement Disorders Nervous System Diseases Neurodegenerative Diseases Parkinson Disease Parkinsonian Disorders Synucleinopathies

Age range

30 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Rush University Medical Center

Chicago, Illinois, 60612, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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%

Treatment and study plan

Primary outcomes

Lipopolysaccharide binding protein (LBP) level

Time frame: one day

measure serum and plasma LBP levels in PD patients and control subjects

Sponsors and collaborators

Lead sponsor

Rush University Medical Center

Other

Registry information

Official study title

Lipopolysaccharide Binding Protein as a Potential Biomarker of Parkinson's Disease

Important dates

Study start: 2013
Primary completion: 2014
Study completion: 2014
First posted: Jul 22, 2013
Registry last updated: Nov 13, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed