Ignite Creation Date:
2025-12-24 @ 9:58 PM
Ignite Modification Date:
2025-12-25 @ 7:35 PM
Study NCT ID:
NCT01547832
Status:
TERMINATED
Last Update Posted:
2018-08-29
First Post:
2012-03-06
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Mutations Associated With Parkinson s Disease
Sponsor:
National Heart, Lung, and Blood Institute (NHLBI)
Organization:
Study Overview
Official Title:
Metabolic Phenotyping of Subjects With Mutations Associated With Hereditary Parkinson's Disease
Status:
TERMINATED
Status Verified Date:
2018-08-27
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Background:
\- Early-onset Parkinson's disease (EOPD) is more likely to be caused by gene mutations than Parkinson's disease that develops in older people. Studying these mutations may help find therapies for EOPD. Researchers want to study mutations on a gene called PARK2. These mutations prevent fat uptake into cells and may interfere with normal brain function. Researchers want to study fat and cholesterol in the body to look at the effects of these mutations on the body and brain.
Objectives:
\- To study connections between genetic mutations and EOPD.
Eligibility:
* Individuals between 18 and 80 years of age with EOPD.
* Individuals between 18 and 80 years of age with no family history of Parkinson s disease.
Design:
* Participants will be screened with a physical exam and medical history. Blood and urine samples will also be collected.
* Participants will have some or all of the following tests:
* Blood samples and tissue (skin and fat) biopsies
* Cell line development from these tissue samples to study the function of PARK2
* DEXA scan to measure body fat context using low dose x-rays
* Glucose and insulin tolerance testing to measure blood sugar levels.
* Treatment will not be provided as part of this protocol.
\- Early-onset Parkinson's disease (EOPD) is more likely to be caused by gene mutations than Parkinson's disease that develops in older people. Studying these mutations may help find therapies for EOPD. Researchers want to study mutations on a gene called PARK2. These mutations prevent fat uptake into cells and may interfere with normal brain function. Researchers want to study fat and cholesterol in the body to look at the effects of these mutations on the body and brain.
Objectives:
\- To study connections between genetic mutations and EOPD.
Eligibility:
* Individuals between 18 and 80 years of age with EOPD.
* Individuals between 18 and 80 years of age with no family history of Parkinson s disease.
Design:
* Participants will be screened with a physical exam and medical history. Blood and urine samples will also be collected.
* Participants will have some or all of the following tests:
* Blood samples and tissue (skin and fat) biopsies
* Cell line development from these tissue samples to study the function of PARK2
* DEXA scan to measure body fat context using low dose x-rays
* Glucose and insulin tolerance testing to measure blood sugar levels.
* Treatment will not be provided as part of this protocol.
Detailed Description:
The majority of subjects with the degenerative Parkinson s Disease present at around the age of 70 years. Other subjects develop this brain disease before the age of 40 years. This early onset presentation is more likely to have a direct genetic cause than the degenerative form of the disease. Our understanding of the genetic causes of early onset Parkinson s Disease may help us find therapies for both the genetic and more degenerative illnesses. Our laboratory has found that one of the genetic mutations associated with early onset Parkinson s Disease, in a gene called PARK2 results in impaired uptake of fat into cells. This may have detrimental effects in the brain, as the brain requires fat to make cholesterol and to send brain signals. A finding in mice lacking PARK2, is that they are resistant to diet induced diabetes and obesity and to fatty liver. These data suggests that the systemic and brain effects of low fat uptake may be opposing, with low fat uptake having a beneficial effect against risk factors such as obesity and diabetes but increasing the risk for brain diseases. To begin to test whether this is the case in subjects with PARK2 mutations we propose to test their fat uptake and glucose and insulin sensitivity.
Study Oversight
Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary ID Infos
| Secondary ID | Type | Domain | Link | View |
|---|---|---|---|---|
| 12-H-0084 | None | None | View |