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December 07, 2010; 75 (23) Articles

Frontal lobe white matter hyperintensities and neurofibrillary pathology in the oldest old

T.M. Polvikoski, E.C.W. van Straaten, F. Barkhof, R. Sulkava, H.J. Aronen, L. Niinistö, M. Oinas, P. Scheltens, T. Erkinjuntti, R.N. Kalaria
First published November 3, 2010, DOI: https://doi.org/10.1212/WNL.0b013e318200d6f9
T.M. Polvikoski
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E.C.W. van Straaten
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F. Barkhof
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R. Sulkava
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H.J. Aronen
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L. Niinistö
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M. Oinas
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P. Scheltens
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T. Erkinjuntti
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Citation
Frontal lobe white matter hyperintensities and neurofibrillary pathology in the oldest old
T.M. Polvikoski, E.C.W. van Straaten, F. Barkhof, R. Sulkava, H.J. Aronen, L. Niinistö, M. Oinas, P. Scheltens, T. Erkinjuntti, R.N. Kalaria
Neurology Dec 2010, 75 (23) 2071-2078; DOI: 10.1212/WNL.0b013e318200d6f9

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Abstract

Background: Current studies suggest an interaction between vascular mechanisms and neurodegenerative processes that leads to late-onset Alzheimer disease (AD). We tested whether AD pathology was associated with white matter hyperintensities (WMH) or cerebral infarcts in the oldest old individuals.

Methods: Brains from 132 subjects over 85 years old, who came to autopsy from the Vantaa 85+ population-based cohort, were scanned by postmortem MRI and examined for neuropathologic changes. Coronal images were analyzed to determine the degree of frontal and parietal periventricular WMH (PVWMH) and deep WMH (DWMH) and cerebral infarcts. Neuropathologic variables included Consortium to Establish a Registry for Alzheimer's Disease scores for neuritic plaques and Braak staging among subjects in 5 groups: normal aging (NA), borderline with insufficient AD pathology, AD, AD plus other pathology, and other primary degenerative diseases.

Results: Frontal DWMH were detected in >50% of the sample. Both frontal PVWMH and DWMH were significantly more extensive in the AD group compared to the NA group or the NA and borderline groups combined. Frontal PVWMH and DWMH were also associated with increased Braak staging (p = 0.03) and the neuritic plaque load (p = 0.01). Further analysis revealed there were a greater number of cerebral infarcts associated with frontal DWMH (p = 0.03) but not with frontal PVWMH.

Conclusions: Our study showed an association between neurofibrillary pathology and frontal PVWMH and DWMH (rather than parietal), as a surrogate of small vessel disease, particularly in very old community-dwelling individuals.

Footnotes

  • Study funding: Work in Newcastle is supported by the Medical Research Council (UK), the Alzheimer's Research Trust (UK), and the National Institutes of Health (NINDS).

  • AD
    Alzheimer disease
    AGD
    argyrophilic grain disease
    CERAD
    Consortium to Establish a Registry for Alzheimer's Disease
    CVD
    cerebrovascular disease
    DLB
    dementia with Lewy bodies
    DTI
    diffusion tensor imaging
    DWMH
    deep white matter hyperintensities
    MR
    magnetic resonance
    NA
    normal aging
    PVWMH
    periventricular white matter hyperintensities
    VaD
    vascular dementia
    WM
    white matter
    WMH
    white matter hyperintensities

  • Supplemental data at www.neurology.org

  • Received July 19, 2009.
  • Accepted August 4, 2010.
  • Copyright © 2010 by AAN Enterprises, Inc.
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