4.7 Article

Florbetapir imaging in cerebral amyloid angiopathy-related hemorrhages

Journal

NEUROLOGY
Volume 89, Issue 7, Pages 697-704

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000004228

Keywords

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Funding

  1. Avid Radiopharmaceuticals
  2. Toulouse Teaching Hospital (CHU)
  3. Institut des Sciences et du Cerveau de Toulouse
  4. French National Agency for Research [ANR-11-LABEX-0018-01]
  5. CHU Toulouse

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Objective: To assess whether F-18-florbetapir, a PET amyloid tracer, could bind vascular amyloid in cerebral amyloid angiopathy (CAA) by comparing cortical florbetapir retention during the acute phase between patients with CAA-related lobar intracerebral hemorrhage (ICH) and patients with hypertension-related deep ICH. Methods: Patients with acute CAA-related lobar ICH were prospectively enrolled and compared with patients with deep ICH. F-18-florbetapir PET, brain MRI, and APOE genotype were obtained for all participants. Cortical florbetapir standard uptake value ratio (SUVr) was calculated with the whole cerebellum used as a reference. Patients with CAA and those with deep ICH were compared for mean cortical florbetapir SUVr values. Results: Fifteen patients with acute lobar ICH fulfilling the modified Boston criteria for probable CAA (mean age = 67 +/- 12 years) and 18 patients with acute deep ICH (mean age = 63 +/- 11 years) were enrolled. Mean global cortical florbetapir SUVr was significantly higher among patients with CAA-related ICH than among patients with deep ICH (1.27 +/- 0.12 vs 1.12 +/- 0.12, p = 0.001). Cortical florbetapir SUVr differentiated patients with CAA-ICH from those with deep ICH (area under the curve 5 0.811; 95% confidence interval [CI] 0.642-0.980) with a sensitivity of 0.733 (95% CI 0.475-0.893) and a specificity of 0.833 (95% CI 0.598-0.948). Conclusions: Cortical florbetapir uptake is increased in patients with CAA-related ICH relative to those with deep ICH. Although F-18-florbetapir PET can label vascular b-amyloid and might serve as an outcome marker in future clinical trials, its diagnostic value in acute CAA-related ICH seems limited in clinical practice.

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