A Longitudinal Study in 1st Degree Relatives of Parkinson's Disease (PD) Patients

NCT ID: NCT01502384

Last Updated: 2011-12-30

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

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-01-31

Brief Summary

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This is a longitudinal study in healthy 1st degree relatives of patients with Parkinson's Disease (PD) carriers of a genetic mutation in genes that are known to increase the risk for PD. The purpose of this study is to explore the association between genetic mutations in the known genes and early preclinical symptoms such as motor, sensory, autonomic, behavioral and cognitive functions.

Detailed Description

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Conditions

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Parkinson's Disease

Keywords

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healthy 1st degree relatives of pd patients

Study Design

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Observational Model Type

COHORT

Study Groups

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healthy relatives

healthy 1st degree relatives of PD patients

neurological examination

Intervention Type OTHER

motor and cognitive functions

Interventions

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neurological examination

motor and cognitive functions

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* healthy 1ST degree relatives of PD patients with known genotype that participated in an earlier genetic study at the sourasky medical center.

Exclusion Criteria

* subjects with cognitive decline by the parameters defined in DSM- IV
* subjects with psychiatric disorder
* subjects unable to sign a consent form
Minimum Eligible Age

35 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Beth Israel Medical Center

OTHER

Sponsor Role collaborator

Columbia University

OTHER

Sponsor Role collaborator

Tel-Aviv Sourasky Medical Center

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Tel Aviv Sourasky Medical Center

Tel Aviv, , Israel

Site Status

Countries

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Israel

Central Contacts

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Anat Mirelman, PhD

Role: CONTACT

Phone: 972-3-6974958

Email: [email protected]

Facility Contacts

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Anat Mirelman, PhD

Role: primary

References

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Di Monte DA. The environment and Parkinson's disease: is the nigrostriatal system preferentially targeted by neurotoxins? Lancet Neurol. 2003 Sep;2(9):531-8. doi: 10.1016/s1474-4422(03)00501-5.

Reference Type BACKGROUND
PMID: 12941575 (View on PubMed)

Di Monte DA, Lavasani M, Manning-Bog AB. Environmental factors in Parkinson's disease. Neurotoxicology. 2002 Oct;23(4-5):487-502. doi: 10.1016/s0161-813x(02)00099-2.

Reference Type BACKGROUND
PMID: 12428721 (View on PubMed)

Huang Y, Cheung L, Rowe D, Halliday G. Genetic contributions to Parkinson's disease. Brain Res Brain Res Rev. 2004 Aug;46(1):44-70. doi: 10.1016/j.brainresrev.2004.04.007.

Reference Type BACKGROUND
PMID: 15297154 (View on PubMed)

Quik M. Smoking, nicotine and Parkinson's disease. Trends Neurosci. 2004 Sep;27(9):561-8. doi: 10.1016/j.tins.2004.06.008.

Reference Type BACKGROUND
PMID: 15331239 (View on PubMed)

Vila M, Przedborski S. Genetic clues to the pathogenesis of Parkinson's disease. Nat Med. 2004 Jul;10 Suppl:S58-62. doi: 10.1038/nm1068.

Reference Type BACKGROUND
PMID: 15272270 (View on PubMed)

von Bohlen und Halbach O, Schober A, Krieglstein K. Genes, proteins, and neurotoxins involved in Parkinson's disease. Prog Neurobiol. 2004 Jun;73(3):151-77. doi: 10.1016/j.pneurobio.2004.05.002.

Reference Type BACKGROUND
PMID: 15236834 (View on PubMed)

Farrer M, Stone J, Mata IF, Lincoln S, Kachergus J, Hulihan M, Strain KJ, Maraganore DM. LRRK2 mutations in Parkinson disease. Neurology. 2005 Sep 13;65(5):738-40. doi: 10.1212/01.wnl.0000169023.51764.b0.

Reference Type BACKGROUND
PMID: 16157908 (View on PubMed)

Wilk JB, Lash TL. Risk factor studies of age-at-onset in a sample ascertained for Parkinson disease affected sibling pairs: a cautionary tale. Emerg Themes Epidemiol. 2007 Apr 4;4:1. doi: 10.1186/1742-7622-4-1.

Reference Type BACKGROUND
PMID: 17408493 (View on PubMed)

Orr-Urtreger A, Shifrin C, Rozovski U, Rosner S, Bercovich D, Gurevich T, Yagev-More H, Bar-Shira A, Giladi N. The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect? Neurology. 2007 Oct 16;69(16):1595-602. doi: 10.1212/01.wnl.0000277637.33328.d8.

Reference Type BACKGROUND
PMID: 17938369 (View on PubMed)

Clark LN, Nicolai A, Afridi S, Harris J, Mejia-Santana H, Strug L, Cote LJ, Louis ED, Andrews H, Waters C, Ford B, Frucht S, Fahn S, Mayeux R, Ottman R, Marder K. Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity. Mov Disord. 2005 Jan;20(1):100-3. doi: 10.1002/mds.20320.

Reference Type BACKGROUND
PMID: 15517591 (View on PubMed)

Thaler A, Ash E, Gan-Or Z, Orr-Urtreger A, Giladi N. The LRRK2 G2019S mutation as the cause of Parkinson's disease in Ashkenazi Jews. J Neural Transm (Vienna). 2009 Nov;116(11):1473-82. doi: 10.1007/s00702-009-0303-0.

Reference Type BACKGROUND
PMID: 19756366 (View on PubMed)

Mirelman A, Gurevich T, Giladi N, Bar-Shira A, Orr-Urtreger A, Hausdorff JM. Gait alterations in healthy carriers of the LRRK2 G2019S mutation. Ann Neurol. 2011 Jan;69(1):193-7. doi: 10.1002/ana.22165.

Reference Type BACKGROUND
PMID: 21280089 (View on PubMed)

Other Identifiers

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TASMC-11-NG-0463

Identifier Type: -

Identifier Source: org_study_id