Literature DB >> 1635663

Quantitative differences in the deposition of beta A4 protein in the sulci and gyri of frontal and temporal isocortex in Alzheimer's disease.

S M Gentleman1, D Allsop, C J Bruton, R Jagoe, J M Polak, G W Roberts.   

Abstract

The distribution of beta-amyloid protein (beta A4) in the frontal and temporal isocortex of 14 Alzheimer's disease brains was examined using a combination of immunohistochemistry and computer image analysis. The area of cortex covered by beta A4 deposits was determined and expressed as a percentage of the total cortical grey matter area in each field of interest. Significantly more beta A4 was found in the grey matter of the sulci as compared to that of the gyral crests in both the frontal and the temporal lobes (P less than 0.05). Furthermore, in each case, greater quantities of beta A4 were observed in the frontal rather than the temporal lobes. This apparent differential vulnerability is likely to reflect underlying anatomical connections or perhaps differences in cell packing density and appears to strengthen the case for an anatomical basis for the spread of the disease pathology.

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Year:  1992        PMID: 1635663     DOI: 10.1016/0304-3940(92)90639-o

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  5 in total

1.  Quantitative neuropathology: an update on automated methodologies and implications for large scale cohorts.

Authors:  Lauren Walker; Kirsty E McAleese; Mary Johnson; Ahmad A Khundakar; Daniel Erskine; Alan J Thomas; Ian G McKeith; Johannes Attems
Journal:  J Neural Transm (Vienna)       Date:  2017-03-06       Impact factor: 3.575

2.  Astroglial tau pathology alone preferentially concentrates at sulcal depths in chronic traumatic encephalopathy neuropathologic change.

Authors:  John D Arena; Victoria E Johnson; Edward B Lee; Garrett S Gibbons; Douglas H Smith; John Q Trojanowski; William Stewart
Journal:  Brain Commun       Date:  2020-12-03

3.  A common brain network links development, aging, and vulnerability to disease.

Authors:  Gwenaëlle Douaud; Adrian R Groves; Christian K Tamnes; Lars Tjelta Westlye; Eugene P Duff; Andreas Engvig; Kristine B Walhovd; Anthony James; Achim Gass; Andreas U Monsch; Paul M Matthews; Anders M Fjell; Stephen M Smith; Heidi Johansen-Berg
Journal:  Proc Natl Acad Sci U S A       Date:  2014-11-24       Impact factor: 11.205

4.  Cortical tau load is associated with white matter hyperintensities.

Authors:  Kirsty E McAleese; Michael Firbank; Madhurima Dey; Sean J Colloby; Lauren Walker; Mary Johnson; Joshua R Beverley; John Paul Taylor; Alan J Thomas; John T O'Brien; Johannes Attems
Journal:  Acta Neuropathol Commun       Date:  2015-09-30       Impact factor: 7.801

5.  Parietal white matter lesions in Alzheimer's disease are associated with cortical neurodegenerative pathology, but not with small vessel disease.

Authors:  Kirsty E McAleese; Lauren Walker; Sophie Graham; Elisa L J Moya; Mary Johnson; Daniel Erskine; Sean J Colloby; Madhurima Dey; Carmen Martin-Ruiz; John-Paul Taylor; Alan J Thomas; Ian G McKeith; Charles De Carli; Johannes Attems
Journal:  Acta Neuropathol       Date:  2017-06-21       Impact factor: 17.088

  5 in total

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