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Review
. 2013 Mar 2:3:11-14.
doi: 10.2147/DNND.S40835. eCollection 2013.

The relationship between the apolipoprotein E e4 allele and hippocampal magnetic resonance imaging volume in community-dwelling individuals with mild Alzheimer's disease

Affiliations
Review

The relationship between the apolipoprotein E e4 allele and hippocampal magnetic resonance imaging volume in community-dwelling individuals with mild Alzheimer's disease

Bernard Walsh et al. Degener Neurol Neuromuscul Dis. .

Abstract

Background: The degree of hippocampal magnetic resonance imaging (MRI) volume loss in Alzheimer's disease (AD) is commonly accepted as a marker of disease severity, yet remains expensive, unavailable, or not tolerated by many patients.

Aim: To examine whether the presence of one or more apolipoprotein E (ApoE) e4 alleles is associated with smaller hippocampal MRI volumes in a population of early AD patients.

Methods: A total of 88 consecutive patients attending a community-based memory disorders clinic who had both mild dementia on the Clinical Dementia Rating scale and Diagnostic and Statistical Manual of Mental Disorders criteria for probable AD were recruited. We examined the relationship between ApoE e4 allele load and hippocampal atrophy on MRI volumes.

Results: There was no association between the ApoE e4 load and hippocampal volume in this cohort.

Conclusion: This study suggests that the presence of one or more ApoE e4 alleles cannot be used to estimate pathological disease load in early AD.

Keywords: Alzheimer’s disease; MRI; apolipoprotein E; hippocampus.

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Conflict of interest statement

Disclosure The authors report no conflicts of interest in this work.

Figures

Figure 1
Figure 1
Age of Alzheimer’s disease onset across apolipoprotein (ApoE) e4 status (0, 1, and 2 × e4 alleles).
Figure 2
Figure 2
Left and right hippocampal volumes across apolipoprotein E e4 load (0, 1, and 2 × e4 alleles).

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References

    1. Morris JC. The Clinical Dementia Rating (CDR): current version and scoring rules. Neurology. 1993;43:2412–2414. - PubMed
    1. Kim J, Basak J, Holtzman D. The role of apolipoprotein E in Alzheimer’s disease. Neuron. 2009;63:287–303. - PMC - PubMed
    1. Baker R, Gholkar A, Scheltens P, et al. ApoE e4 allele, temporal lobe atrophy, and white matter lesions in late life dementias. Arch Neurol. 1999;56:961–965. - PubMed
    1. Geroldi C, Pihlajamäki M, Laakso M, et al. APOE-epsilon4 is associated with less frontal and more medial lobe atrophy in AD. Neurology. 1999;53:1825–1832. - PubMed
    1. Jack CR, Jr, Petersen RC, Xu YC, et al. Hippocampal atrophy and apolipoprotein E genotype are independently associated with Alzheimer’s disease. Ann Neurol. 1998;43:303–310. - PMC - PubMed