Evaluation of a Biomarker Related to the GI Tract for the Diagnosis of Parkinson's Disease

NCT01904240 | Completed

• 1 other identifier: 12102401-IRB01
• Study Type: observational
• Target: 200
• Locations: 1 country
• Sites: 1

Brief Summary

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.

Conditions

Parkinson's Disease

Keywords

Parkinson's disease; GI tract; Lipopolysaccharide binding protein

Outcome Measures

Primary Outcomes (1)

• Lipopolysaccharide binding protein (LBP) level

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

  one day

Study Arms (2)

Parkinson's disease patients

Patients with Parkinson's disease

Subjects without Parkinson's disease

Control subjects without Parkinson's disease

Eligibility Criteria

• Age: 30 Years - 90 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Rush University Movement Disorders Clinic

You may qualify if:

• 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.

You may not qualify if:

• 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%
• 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.
• 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%

Sponsors & Collaborators

• Rush University Medical Center: lead

Study Sites (1)

Rush University Medical Center

Chicago, Illinois, 60612, United States

Location

MeSH Terms

Conditions

Parkinson Disease

Condition Hierarchy (Ancestors)

Parkinsonian Disorders; Basal Ganglia Diseases; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Movement Disorders; Synucleinopathies; Neurodegenerative Diseases

Study Officials

• Gian D Pal, MD

  Rush University Medical Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: CASE CONTROL
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 9, 2013
• First Posted: July 22, 2013
• Study Start: July 1, 2013
• Primary Completion: June 1, 2014
• Study Completion: June 1, 2014
• Last Updated: November 13, 2014

Record last verified: 2014-11

Locations

US (1)