Diagnostic Accuracy of MRI and Additional [18F]FDG-PET for Behavioral Variant Frontotemporal Dementia in Patients with Late Onset Behavioral Changes

Everard G B Vijverberg, Mike P Wattjes, Annemiek Dols, Welmoed A Krudop, Christiane Möller, Anne Peters, Cora J Kerssens, Flora Gossink, Niels D Prins, Max L Stek, Philip Scheltens, Bart N M van Berckel, Frederik Barkhof, Yolande A L Pijnenburg

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

BACKGROUND: Neuroimaging has a reasonable accuracy to differentiate behavioral variant frontotemporal dementia (bvFTD) from other neurodegenerative disorders, its value for the differentiation of bvFTD among subjects with acquired behavioral disturbances is unknown.

OBJECTIVE: To determine the diagnostic accuracy of MRI, additional [18F]FDG-PET, and their combination for bvFTD among subjects with late onset behavioral changes.

METHODS: Patients with late onset behavioral changes referred to a memory clinic or psychiatric services were included. At baseline, 111 patients had a brain MRI scan and 74 patients received an additional [18F]FDG-PET when the MRI was inconclusive. The consensus diagnosis after two-year-follow-up was used as the gold standard to calculate sensitivity and specificity for baseline neuroimaging.

RESULTS: 27 patients had probable/definite bvFTD and 84 patients had a non-bvFTD diagnosis (primary psychiatric diagnosis or other neurological disorders). MRI had a sensitivity of 70% (95% CI 52-85%) with a specificity of 93% (95% CI 86-97%). Additional [18F]FDG-PET had a sensitivity of 90% (95% CI 66-100%) with a specificity of 68% (95% CI 56-79%). The sensitivity of combined neuroimaging was 96% (95% CI 85-100%) with a specificity of 73% (95% CI 63-81%). In 66% of the genetic FTD cases, MRI lacked typical frontotemporal atrophy. 40% of cases with a false positive [18F]FDG-PET scan had a primary psychiatric diagnosis.

CONCLUSION: A good diagnostic accuracy was found for MRI and additional [18F]FDG-PET for bvFTD in patients with late onset behavioral changes. Caution with the interpretation of neuroimaging results should especially be taken in cases with a genetic background and in cases with a primary psychiatric differential diagnosis where [18F]FDG-PET is the only abnormal investigation.

Original languageEnglish
Pages (from-to)1287-97
Number of pages11
JournalJournal of Alzheimer's Disease
Volume53
Issue number4
DOIs
Publication statusPublished - 30 Jun 2016

Keywords

  • Age of Onset
  • Aged
  • Atrophy
  • Brain/diagnostic imaging
  • False Negative Reactions
  • False Positive Reactions
  • Female
  • Fluorodeoxyglucose F18
  • Follow-Up Studies
  • Frontotemporal Dementia/diagnostic imaging
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mental Disorders/diagnostic imaging
  • Middle Aged
  • Neuroimaging
  • Positron-Emission Tomography
  • Prospective Studies
  • Radiopharmaceuticals
  • Sensitivity and Specificity

Fingerprint

Dive into the research topics of 'Diagnostic Accuracy of MRI and Additional [18F]FDG-PET for Behavioral Variant Frontotemporal Dementia in Patients with Late Onset Behavioral Changes'. Together they form a unique fingerprint.

Cite this