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PMID: 16116614 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.

Pankratz N, Byder L, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T, Nichols WC

Abstract

The epsilon4 allele of the apolipoprotein E gene (APOE4) has been consistently associated with a greater risk of Alzheimer's disease (AD) as well as an earlier onset of AD. It is possible that APOE4 may also play a role in the etiology of other neurodegenerative disorders, such as Parkinson's disease (PD). APOE genotype, age of onset, disease duration, smoking history, and dementia status were collected for families with PD, yielding 324 Caucasian families with complete information. Logistic regression employing one individual per family and including age of onset and disease duration as covariates demonstrated a significantly increased risk of dementia for those individuals having inherited at least one epsilon4 allele (OR=3.37; P=0.002). Survival analyses also demonstrated a significantly earlier age of onset for those subjects with at least one epsilon4 allele (59.7 years) as compared with those homozygous for the more common epsilon3 allele (62.4 years; P=0.009). Thus, consistent with previous studies, we find evidence that the presence of an epsilon4 allele results in significantly earlier onset of PD and a greater likelihood of dementia. It appears the similarities between PD and AD may be due to an overlap in the diseases' genetic etiology.

MeSH Terms
Adolescent Adult Aged Aged, 80 and over Alleles Alzheimer Disease/genetics Apolipoprotein E4 Apolipoproteins E/genetics Female Genetic Carrier Screening Genotype Homozygote Humans Lewy Body Disease/genetics Male Mental Status Schedule Middle Aged Neurologic Examination Neuropsychological Tests Parkinson Disease/genetics Risk Statistics as Topic Survival Analysis
Chemicals
Apolipoprotein E4 Apolipoproteins E
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Pankratz Nathan
Department of Medical and Molecular Genetics, Indiana University Medical Center, Indianapolis, Indiana, USA.
Byder Lisa
Halter Cheryl
Rudolph Alice
Shults Clifford W
Conneally P Michael
Foroud Tatiana
Nichols William C
Article Info
Journal
Movement disorders : official journal of the Movement Disorder Society
Abbr.
Mov Disord
ISSN
0885-3185
Published
2006-01-00
Pages
45-9
Language
English
Region
United States
NLM ID
8610688
Subset
IM
Grants
NINDS NIH HHS · R01 NS37167 · United States
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