Diagnostic and Prognostic Biomarkers in Parkinson Disease

Parkinson Disease Clinical Trial

— PROBE  

Official title:

Blood Alpha-Synuclein, Gene Expression, and Smell Testing as Diagnostic and Prognostic Biomarkers in Parkinson's Disease

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00653783
• Other study ID #: U01NS050095-02_PROBE
• Secondary ID: DOD Grant # W81X
• Status: Active, not recruiting
• Phase: N/A
• First received: April 2, 2008
• Last updated: December 30, 2008
• Start date: August 2007

Study information

• Verified date: December 2008
• Source: The Parkinson Study Group
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

The overall goal of PROBE is to evaluate the feasibility and potential utility of three markers (alpha-synuclein, transcriptomic profiles and olfactory function) to determine the risk or prognosis of PD.

Description:

PROBE will test three biomarkers in PD subjects and controls to determine their feasibility and potential utility as markers of risk and prognosis for PD. This is a case control study, in which PD subjects will be compared to neurologically healthy controls and disease controls (MSA and PSP). The blood biomarker samples will be drawn once to evaluate blood alpha-synuclein levels as well as collection of lymphocyte mass for array analysis. Olfaction will be measured using the UPSIT for all subjects. The UPSIT will be conducted as part of PostCEPT for PD subjects and will only be repeated in this study for PD subjects in not done within 6 months. Control subjects may also choose to submit a blood specimen for processing and storage at the Coriell Institute for Medical Research, a research resource supported by the NINDS Human Genetics Resource Center.

Follow-up of the PD population over a 3-year period will allow us to evaluate the prognosis for important motor aspects of PD that will occur frequently in this cohort. These complications of PD include motor complications, postural instability, and non-motor impairment such as cognitive decline.

Healthy and disease control subjects may give permission at the Baseline visit to be contacted and followed in the previously established PSG FOUND study using mail and telephone contact to assess clinical status. Participation in the FOUND study provides another mechanism to maintain contact with subjects and collect supplemental data beyond that collected at the PROBE Baseline visit.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 200
• Est. primary completion date: July 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years and older

Eligibility

Parkinson Disease Inclusion Criteria:

• Subject is participating in PostCEPT and meets UK brain bank criteria for PD

• Willing and able to provide informed consent

Healthy Control Inclusion Criteria:

• Spouse or non blood relative of the PD subject

• No known current diagnosis or history of a neurological disease

• MMSE score >27

• Age >45

• Willing and able to provide informed consent

Parkinsonism/Disease Control Inclusion Criteria (MSA and PSP)

• A diagnosis of Probable MSA based on Consensus Criteria OR Probable PSP based on NINDS-PSP Criteria

• Willing and able to provide informed consent

Exclusion Criteria for All Groups:

• Current use (within 7 days prior to Baseline Visit) of anticoagulants (e.g., warfarin or heparin)

• Known bleeding disorder (acquired or inherited)

• Known blood disorder (e.g. leukemia) or a history of anemia with a documented hematocrit <30

• Known pregnancy

• History of nasal trauma, sinusitis, or other nasal pathology that would interfere with smell testing

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

• Multiple System Atrophy
• Parkinson Disease
• Progressive Supranuclear Palsy
• Shy-Drager Syndrome
• Supranuclear Palsy, Progressive

Locations

Country	Name	City	State
United States	Parkinson Study Group	Rochester	New York

Sponsors (2)

Lead Sponsor	Collaborator
The Parkinson Study Group	United States Department of Defense

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	a-synuclein, transcriptomic profiles and olfactory function		Three years	No
Secondary	Unified Parkinson Disease Rating Scale (UPDRS)		Three Years	No
Secondary	University of Pennsylvania Smell Identification Test (UPSIT)		Three Years	No