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Tracking Alzheimer's disease.

Tracking Alzheimer's disease. Research Abstract Details 

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  • Tracking Alzheimer's disease. Abstract Text:

    paul m thompsonPaul M Thompson,kiralee m hayashiKiralee M Hayashi,rebecca a duttonRebecca A Dutton,ming-chang chiangMing-Chang Chiang,alex d leowAlex D Leow,elizabeth r sowellElizabeth R Sowell,greig de zubicarayGreig De Zubicaray,james t beckerJames T Becker,oscar l lopezOscar L Lopez,howard j aizensteinHoward J Aizenstein,arthur w togaArthur W Toga,

    Population-based brain mapping provides great insight into the trajectory of aging and dementia, as well as brain changes that normally occur over the human life span. We describe three novel brain mapping techniques, cortical thickness mapping, tensor-based morphometry (TBM), and hippocampal surface modeling, which offer enormous power for measuring disease progression in drug trials, and shed light on the neuroscience of brain degeneration in Alzheimer's disease (AD) and mild cognitive impairment (MCI). We report the first time-lapse maps of cortical atrophy spreading dynamically in the living brain, based on averaging data from populations of subjects with Alzheimer's disease and normal subjects imaged longitudinally with MRI. These dynamic sequences show a rapidly advancing wave of cortical atrophy sweeping from limbic and temporal cortices into higher-order association and ultimately primary sensorimotor areas, in a pattern that correlates with cognitive decline. A complementary technique, TBM, reveals the 3D profile of atrophic rates, at each point in the brain. A third technique, hippocampal surface modeling, plots the profile of shape alterations across the hippocampal surface. The three techniques provide moderate to highly automated analyses of images, have been validated on hundreds of scans, and are sensitive to clinically relevant changes in individual patients and groups undergoing different drug treatments. We compare time-lapse maps of AD, MCI, and other dementias, correlate these changes with cognition, and relate them to similar time-lapse maps of childhood development, schizophrenia, and HIV-associated brain degeneration. Strengths and weaknesses of these different imaging measures for basic neuroscience and drug trials are discussed.

    Tracking Alzheimer's disease. Publishing Authors By Initials

    pm thompsonPM Thompson,km hayashiKM Hayashi,ra duttonRA Dutton,mc chiangMC Chiang,ad leowAD Leow,er sowellER Sowell,g de zubicarayG De Zubicaray,jt beckerJT Becker,ol lopezOL Lopez,hj aizensteinHJ Aizenstein,aw togaAW Toga,

    For similar tomography, emission-computed: positron-emission tomography research abstracts see: tomography, emission-computed: positron-emission tomography research

    PUBMED ID PMID:

    MEDLINE DATE:

    Tracking Alzheimer's disease. Journal Published:

    PUBLICATION TYPE: Review

    Journal: Annals of the New York Academy of Sciences

    VOLUME: 1097

    Page Numbers: 183-214

    Journal Abbreviation:

    ISSN: 0077-8923

    DAY: 3

    MONTH: Feb

    YEAR: 2007

    Tracking Alzheimer's disease. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7506858

    Tracking Alzheimer's disease. Keywords Mesh Terms:

    KEYWORDS: Positron-Emission Tomography

    MESH TERMS: therapeutic use

    Chemical & Substance for Abstract: Tracking Alzheimer's disease. Information

    Substance Name: Nootropic Agents

    Registry Number: 0

    Grant and Affiliation Information for Tracking Alzheimer's disease.

    AFFILIATION: Department of Neurology, Laboratory of Neuro Imaging, UCLA School of Medicine, 635 Charles E. Young Drive South, Suite 225E, Los Angeles, CA 90095-7332, USA. thompson@loni.ucla.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCRR

    GRANT: RR13642

    ACRONYM: RR

    MEDLINETA: Ann N Y Acad Sci

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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