Neuroinflammation in frontotemporal lobar degeneration revealed by 11 C-PBR28 PET

Ann Clin Transl Neurol. 2019 Jul;6(7):1327-1331. doi: 10.1002/acn3.50802. Epub 2019 Jun 17.

Abstract

This study used 11 C-PBR28 positron emission tomography (PET) imaging to determine whether levels of 18-kDa translocator protein (TSPO), an inflammation-specific biomarker, are increased in frontotemporal lobar degeneration (FTLD) patients. 11 C-PBR28, 18 F-FDG, and 11 C-PIB brain PET scans, as well as magnetic resonance imaging (MRI), were conducted in four FTLD patients and 22 healthy controls. 11 C-PBR28 scans revealed that all FTLD patients showed increased TSPO binding versus controls. Significantly greater increases in TSPO were observed in the frontal, lateral temporal, parietal, and occipital cortices, topographically consistent with individual clinical phenotypes and with brain MRI and 18 F-FDG PET. Amyloid burden was not increased.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Adult
  • Aged
  • Carbon Radioisotopes
  • Female
  • Fluorodeoxyglucose F18
  • Frontotemporal Lobar Degeneration / diagnostic imaging*
  • Frontotemporal Lobar Degeneration / metabolism*
  • Frontotemporal Lobar Degeneration / pathology
  • Humans
  • Male
  • Middle Aged
  • Positron-Emission Tomography / methods*
  • Radiopharmaceuticals
  • Receptors, GABA / metabolism*

Substances

  • Carbon Radioisotopes
  • Carbon-11
  • Radiopharmaceuticals
  • Receptors, GABA
  • TSPO protein, human
  • Fluorodeoxyglucose F18