Literature DB >> 12020270

Familial aggregation of Parkinson disease: a comparative study of early-onset and late-onset disease.

Haydeh Payami1, Sepideh Zareparsi, Dora James, John Nutt.   

Abstract

CONTEXT: It is unclear whether late-onset Parkinson disease (PD), which is the most typical and most common form of the disease, has a familial component. Evidence for familial aggregation is key to whether research should focus on gene discovery or search for environmental factors.
OBJECTIVE: To investigate familial aggregation of early-onset and late-onset PD separately.
METHODS: Using survival methods, age-specific risk of PD was calculated and compared for 525 parents and siblings of 117 patients with early-onset PD, 1642 parents and siblings of 343 patients with late-onset PD, and 522 parents and siblings of 114 controls. The index patients were ascertained from a movement disorder clinic. Spouses and friends served as controls.
RESULTS: Compared with the relatives of controls, age-specific risk of PD was increased 7.76-fold in the relatives of patients with early-onset disease (P<.001) and 2.95-fold in the relatives of those with late-onset disease (P =.02).
CONCLUSIONS: Late-onset PD has a significant familial component. The magnitude of recurrence risk to relatives suggests a genetic etiology, without ruling out the possibility of a coexisting environmental component.

Entities:  

Mesh:

Year:  2002        PMID: 12020270     DOI: 10.1001/archneur.59.5.848

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  20 in total

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9.  Evidence of shared risk for Alzheimer's disease and Parkinson's disease using family history.

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10.  Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.

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Journal:  Hum Mol Genet       Date:  2012-08-13       Impact factor: 6.150

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