Haptoglobin and Iron in Parkinson's Disease

NCT ID: NCT02422992

Last Updated: 2016-11-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

342 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-02-28

Study Completion Date

2016-06-30

Brief Summary

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This is a case/control epidemiology study to identify what are the iron-metabolism abnormalities in Parkinson's disease (PD) patients, and risk factors relevant to PD predisposition.

Detailed Description

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A total of 342 participants, 100 PD patients and 242 age- and gender matched controls, were included in the study. All study participants were seen for one study visit in the morning at one of two Bastyr University Clinics in the Seattle area. Study participants were fasting at the time of the visit. During the study visit, participants donated a blood sample for the blood tests and complete an epidemiology questionnaire.

A subset of 51 of the study participant who were seen for the visit at Bastyr University, underwent brain scan and Magnetic Resonance Imaging (MRI), at the University of Washington Department of Radiology. The MRI part of the study aims at estimating brain iron levels.

Conditions

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Parkinson's Disease

Keywords

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Iron metabolism MRI risk factors haptoglobin phenotype

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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PD

100 PD patients were patients diagnosed with Parkinson's disease

No interventions assigned to this group

Controls

242 Controls were subjects free of neurodegenerative diseases, matched by age and gender to the PD patients

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Volunteers should be of age between 52 and 82 years of age, males of females.


Diagnosis of Parkinson's disease (UKBB clinical criteria).

Exclusion Criteria

* presence of a neurodegenerative disease,
* presence of active cancer under treatment,
* HIV sero-positivity, Hepatitis B, C, of A sero-positivity
* rheumatoid arthritis
* recent blood donation (less than three months before the visit).
* fever at the time of the visit


* Presence of other neurodegenerative diseases, apart for Parkinson's disease
* two or more family members with Parkinson's disease
* presence of active cancer under treatment
* HIV sero-positivity, Hepatitis B, C, of A sero-positivity
* rheumatoid arthritis
* recent blood donation (less than three months before the visit).
* fever at the time of the visit


* presence in the body of a ferro-magnetic metallic foreign object such as, but not limited to:
* a cardiac pacemaker
* aneurism clip
* neuro-stimulator
* surgical clip
* artificial limb or joint
* orthopedic items, such as screws, nails, pins, rods,
* any metallic foreign body from a previous injury, bullets, shrapnels, metal slivers.
Minimum Eligible Age

35 Years

Maximum Eligible Age

92 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Washington

OTHER

Sponsor Role collaborator

Bastyr University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Paola Costa-Mallen, PhD

Role: PRINCIPAL_INVESTIGATOR

Bastyr University

Locations

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University of California

San Diego, California, United States

Site Status

Bastyr University Research Institute

Kenmore, Washington, United States

Site Status

University of Washington

Seattle, Washington, United States

Site Status

Countries

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United States

References

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Costa-Mallen P, Checkoway H, Zabeti A, Edenfield MJ, Swanson PD, Longstreth WT Jr, Franklin GM, Smith-Weller T, Sadrzadeh SM. The functional polymorphism of the hemoglobin-binding protein haptoglobin influences susceptibility to idiopathic Parkinson's disease. Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):216-22. doi: 10.1002/ajmg.b.30593.

Reference Type BACKGROUND
PMID: 17918239 (View on PubMed)

Other Identifiers

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12A-1330

Identifier Type: -

Identifier Source: org_study_id