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e4/e4 AD patients show markedly more APP
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deposition in plaques relative to non-e4 AD
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patients
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ApoE e4 binds BA4 peptide with greater avidity
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than e3 isoform.
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ApoE e4 shows significant allelic association in
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familial and sporadic late onset
AD, and in familial
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early onset AD.
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e4 heterozygote is 3X more likely to be affected than
e2/e3
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or e3/e3
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e4 homozygote is 8X more likely to be affected
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Conclusion: ApoE e4 gene dose is a major
risk factor
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for late (and possibly early) onset AD. Inheritance
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of two e4 alleles is not
necessary and probably not
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sufficient to cause AD.
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