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Severe cerebral amyloid angiopathy in Alzheimer's disease is associated with frequent old microinfarcts
Author(s) -
Soontornniyomkij Virawudh,
Lynch Matthew D.,
Pomakian Justine,
Clare Ryan,
Vinters Harry V.
Publication year - 2008
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.22.1_supplement.707.3
Subject(s) - cerebral amyloid angiopathy , pathology , alzheimer's disease , cd68 , medicine , white matter , cerebral cortex , immunohistochemistry , magnetic resonance imaging , disease , dementia , radiology
To investigate whether the presence of severe cerebral amyloid angiopathy (CAA) in Alzheimer's disease (AD) was associated with a higher prevalence of old microinfarcts (OMIs) than in AD without significant CAA, 6 AD brains with severe CAA were selected, together with 12 age‐matched AD brains without significant CAA, from the Alzheimer's Disease Research Center Tissue Bank. Immunohistochemistry for CD68 was employed to highlight ≤5 mm foci of macrophage‐infiltrated tissue destruction (i.e. OMIs) in formalin‐fixed paraffin‐embedded tissue blocks taken from various regions of the cerebral cortex/white matter and cerebellum (range 13–21, mean 16.3 blocks per brain in the AD/CAA group; range 7–21, mean 14.7 blocks per brain in the AD group; p = 0.39, 2‐tailed Student's t‐Test). OMIs, manually counted by light microscopy, were observed in all of 6 AD/CAA brains, and in 2 out of 12 AD brains ( p = 0.0015, 2‐tailed Fisher's Exact Test). The number of OMIs per block ranged from 0.14 to 1.76 (mean 0.74) in the AD/CAA group, and from 0 to 0.12 (mean 0.02) in the AD group ( p = 0.02, 1‐tailed Student's t‐Test). Using Perl's iron staining, old microhemorrhages were occasionally seen in both groups. In conclusion, OMIs are frequent in AD with severe CAA, which may contribute to a vascular component of cognitive impairment. This work was supported by the grants P50 AG16570, P01 AG12435 and the Sarkaria Chair in Diagnostic Medicine (H.V.V.).