Correlation of hypointensities in susceptibility-weighted images to tissue histology in dementia patients with cerebral amyloid angiopathy: A postmortem MRI study

Matthew Schrag, Grant McAuley, Justine Pomakian, Arshad Jiffry, Spencer Tung, Claudius Mueller, Harry V. Vinters, E. Mark Haacke, Barbara Holshouser, Daniel Kido, Wolff M. Kirsch

Research output: Contribution to journalArticlepeer-review

Abstract

Neuroimaging with iron-sensitive MR sequences [gradient echo T2* and susceptibility-weighted imaging (SWI)] identifies small signal voids that are suspected brain microbleeds. Though the clinical significance of these lesions remains uncertain, their distribution and prevalence correlates with cerebral amyloid angiopathy (CAA), hypertension, smoking, and cognitive deficits. Investigation of the pathologies that produce signal voids is necessary to properly interpret these imaging findings. We conducted a systematic correlation of SWI-identified hypointensities to tissue pathology in postmortem brains with Alzheimer's disease (AD) and varying degrees of CAA. Autopsied brains from eightADpatients, six of which showed advanced CAA, were imaged at 3T; foci corresponding to hypointensities were identified and studied histologically. A variety of lesions was detected; the most common lesions were acute microhemorrhage, hemosiderin residua of old hemorrhages, and small lacunes ringed by hemosiderin. In lesions where the bleeding vessel could be identified, β-amyloid immunohistochemistry confirmed the presence of β-amyloid in the vessel wall. Significant cellular apoptosis was noted in the perifocal region of recent bleeds along with heme oxygenase 1 activity and late complement activation. Acutely extravasated blood and hemosiderin were noted to migrate through enlarged Virchow-Robin spaces propagating an inflammatory reaction along the local microvasculature; a mechanism that may contribute to the formation of lacunar infarcts. Correlation of imaging findings to tissue pathology in our cases indicates that a variety of CAA-related pathologies produce MR-identified signal voids and further supports the use of SWI as a biomarker for this disease. © Springer-Verlag 2009.
Original languageEnglish
Pages (from-to)291-302
Number of pages12
JournalActa Neuropathologica
Volume119
Issue number3
DOIs
StatePublished - Mar 2010

ASJC Scopus Subject Areas

  • Pathology and Forensic Medicine
  • Clinical Neurology
  • Cellular and Molecular Neuroscience

Keywords

  • Alzheimer's disease
  • Blooming effect
  • Cerebral amyloid angiopathy
  • Complement C6
  • Microbleeds
  • Microinfarcts
  • Susceptibility-weighted imaging
  • Immunohistochemistry
  • Coloring Agents
  • Complement C6/metabolism
  • Humans
  • Male
  • Hemosiderin/metabolism
  • Nerve Tissue Proteins/metabolism
  • Brain Ischemia/etiology
  • Female
  • Alzheimer Disease/pathology
  • Cerebral Amyloid Angiopathy/metabolism
  • Dissection
  • Dementia/pathology
  • Inflammation/pathology
  • Intracranial Hemorrhages/pathology
  • Blood Vessels/pathology
  • Disease Progression
  • Magnetic Resonance Imaging
  • Image Processing, Computer-Assisted
  • Aged
  • Fluorescent Dyes

Cite this