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Neuroimaging measures as endophenotypes in Alzheimer's disease.


ABSTRACT: Late onset Alzheimer's disease (AD) is moderately to highly heritable. Apolipoprotein E allele ?4 (APOE4) has been replicated consistently as an AD risk factor over many studies, and recently confirmed variants in other genes such as CLU, CR1, and PICALM each increase the lifetime risk of AD. However, much of the heritability of AD remains unexplained. AD is a complex disease that is diagnosed largely through neuropsychological testing, though neuroimaging measures may be more sensitive for detecting the incipient disease stages. Difficulties in early diagnosis and variable environmental contributions to the disease can obscure genetic relationships in traditional case-control genetic studies. Neuroimaging measures may be used as endophenotypes for AD, offering a reliable, objective tool to search for possible genetic risk factors. Imaging measures might also clarify the specific mechanisms by which proposed risk factors influence the brain.

SUBMITTER: Braskie MN 

PROVIDER: S-EPMC3087508 | biostudies-literature | 2011 Mar

REPOSITORIES: biostudies-literature

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Neuroimaging measures as endophenotypes in Alzheimer's disease.

Braskie Meredith N MN   Ringman John M JM   Thompson Paul M PM  

International journal of Alzheimer's disease 20110331


Late onset Alzheimer's disease (AD) is moderately to highly heritable. Apolipoprotein E allele ε4 (APOE4) has been replicated consistently as an AD risk factor over many studies, and recently confirmed variants in other genes such as CLU, CR1, and PICALM each increase the lifetime risk of AD. However, much of the heritability of AD remains unexplained. AD is a complex disease that is diagnosed largely through neuropsychological testing, though neuroimaging measures may be more sensitive for dete  ...[more]

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