Alzheimer’s Research & Therapy (Feb 2022)

Amyloid PET imaging and dementias: potential applications in detecting and quantifying early white matter damage

  • Anna M. Pietroboni,
  • Annalisa Colombi,
  • Tiziana Carandini,
  • Luca Sacchi,
  • Chiara Fenoglio,
  • Giorgio Marotta,
  • Andrea Arighi,
  • Milena A. De Riz,
  • Giorgio G. Fumagalli,
  • Massimo Castellani,
  • Marco Bozzali,
  • Elio Scarpini,
  • Daniela Galimberti

DOI
https://doi.org/10.1186/s13195-021-00933-1
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 8

Abstract

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Abstract Purpose Positron emission tomography (PET) with amyloid tracers (amy-PET) allows the quantification of pathological amyloid deposition in the brain tissues, including the white matter (WM). Here, we evaluate amy-PET uptake in WM lesions (WML) and in the normal-appearing WM (NAWM) of patients with Alzheimer’s disease (AD) and non-AD type of dementia. Methods Thirty-three cognitively impaired subjects underwent brain magnetic resonance imaging (MRI), Aβ1-42 (Aβ) determination in the cerebrospinal fluid (CSF) and amy-PET. Twenty-three patients exhibiting concordant results in both CSF analysis and amy-PET for cortical amyloid deposition were recruited and divided into two groups, amyloid positive (A+) and negative (A−). WML quantification and brain volumes’ segmentation were performed. Standardized uptake values ratios (SUVR) were calculated in the grey matter (GM), NAWM and WML on amy-PET coregistered to MRI images. Results A+ compared to A− showed a higher WML load (p = 0.049) alongside higher SUVR in all brain tissues (p < 0.01). No correlations between CSF Aβ levels and WML and NAWM SUVR were found in A+, while, in A−, CSF Aβ levels were directly correlated to NAWM SUVR (p = 0.04). CSF Aβ concentration was the only predictor of NAWM SUVR (adj R 2 = 0.91; p = 0.04) in A−. In A+ but not in A− direct correlations were identified between WM and GM SUVR (p < 0.01). Conclusions Our data provide evidence on the role of amy-PET in the assessment of microstructural WM injury in non-AD dementia, whereas amy-PET seems less suitable to assess WM damage in AD patients due to a plausible amyloid accrual therein.

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