Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1996-6-13
pubmed:abstractText
Apolipoprotein E type 4 allele (apoE epsilon4) is associated with Alzheimer's disease (AD) in the late-onset familial form and in sporadic cases, but the age-associated risk in a randomly sampled elderly population is not established. We examined the association of apoE epsilon4 with AD and other dementias (mainly multi-infarct or dementia following stroke) in 1,030 persons aged 71 to 100 years in the population-based Framingham Study cohort. Kaplan-Meier survival analysis revealed that 55% of the apoE epsilon4/epsilon4 homozygotes developed AD by age 80, whereas 27% of apoE epsilon3/epsilon4 heterozygotes developed AD by age 85, and 9% of those without a 4 allele developed AD by age 85 years. In comparison with persons without a 4 allele, the risk ration for AD was 3.7 (95% CI = 1.9 to 7.5) for apoE epsilon3/epsilon4 heterozygotes and 30.1 (95% CI = 10.7 to 84.4) for apoE epsilon4 homozygotes. ApoE epsilon2 (2/2, 2/3, or 2/4 genotypes) was associated with an absence of AD. One-half (n=21) of the 43 AD patients were either homozygous or heterozygous for apoE epsilon4. We found evidence for an association of apoE epsilon4 with other dementia, primarily multi-infarct dementia and stroke. The risk ratio was 2.3 (95% CI = 0.9 to 6.1) for non-AD dementias among persons with apoE epsilon3/epsilon4. Although the apoE epsilon4 allele is a potent risk factor for AD and may be associated with other forms of dementia, most apoE epsilon4 carriers do not develop dementia, and about one-half of AD is not apoE epsilon4 associated. The low positive predictive value of this marker (0.10) suggest that use of apoE genotyping as a screening test for AD is not supported.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0028-3878
pubmed:author
pubmed:issnType
Print
pubmed:volume
46
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
673-7
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:8618665-Adult, pubmed-meshheading:8618665-Aged, pubmed-meshheading:8618665-Aged, 80 and over, pubmed-meshheading:8618665-Alleles, pubmed-meshheading:8618665-Alzheimer Disease, pubmed-meshheading:8618665-Apolipoprotein E4, pubmed-meshheading:8618665-Apolipoproteins E, pubmed-meshheading:8618665-Base Sequence, pubmed-meshheading:8618665-Cohort Studies, pubmed-meshheading:8618665-Dementia, pubmed-meshheading:8618665-Female, pubmed-meshheading:8618665-Humans, pubmed-meshheading:8618665-Incidence, pubmed-meshheading:8618665-Longitudinal Studies, pubmed-meshheading:8618665-Male, pubmed-meshheading:8618665-Middle Aged, pubmed-meshheading:8618665-Molecular Probes, pubmed-meshheading:8618665-Molecular Sequence Data, pubmed-meshheading:8618665-Odds Ratio, pubmed-meshheading:8618665-Sensitivity and Specificity
pubmed:year
1996
pubmed:articleTitle
Apolipoprotein E epsilon4 association with dementia in a population-based study: The Framingham study.
pubmed:affiliation
Department of Neurology, Boston University School of Medicine, Boston, MA 02118, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.