Positron emission tomography/computerized tomography in newly diagnosed patients with giant cell arteritis who are taking glucocorticoids

Alison H. Clifford, Elana M. Murphy, Steven C. Burrell, Mathew P. Bligh, Ryan F. MacDougall, J. Godfrey Heathcote, Mathieu C. Castonguay, Min S. Lee, Kara Matheson, John G. Hanly

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30 Citations (Scopus)

Résumé

Objective. Large vessel uptake on positron emission tomography/computerized tomography (PET/CT) supports the diagnosis of giant cell arteritis (GCA). Its value, however, in patients without arteritis on temporal artery biopsy and in those receiving glucocorticoids remains unknown. We compared PET/CT results in GCA patients with positive (TAB+) and negative temporal artery biopsies (TAB.), and controls. Methods. Patients with new clinically diagnosed GCA starting treatment with glucocorticoids underwent temporal artery biopsy and PET/CT. Using a visual semiquantitative approach, 18F-fluorodeoxyglucose (FDG) uptake was scored in 8 vascular territories and summed overall to give a total score in patients and matched controls. Results. Twenty-eight patients with GCA and 28 controls were enrolled. Eighteen patients with GCA were TAB+. Mean PET/CT scores after an average of 11.9 days of prednisone were higher in patients with GCA compared to controls, for both total uptake (10.34 ± 2.72 vs 7.73 ± 2.56; p = 0.001), and in 6 of 8 specific vascular territories. PET/CT scores were similar between TAB+ and TAB. patients with GCA. The optimal cutoff for distinguishing GCA cases from controls was a total PET/CT score of ≥ 9, with an area under the receiver-operating characteristic curve of 0.75, sensitivity 71.4%, and specificity 64.3%. Among patients with GCA, these measures correlated with greater total PET/CT scores: systemic symptoms (p = 0.015), lower hemoglobin (p = 0.009), and higher platelet count (p = 0.008). Conclusion. Vascular FDG uptake scores were increased in most patients with GCA despite exposure to prednisone; however, the sensitivity and specificity of PET/CT in this setting were lower than those previously reported.

Langue d'origineEnglish
Pages (de-à)1859-1866
Nombre de pages8
JournalJournal of Rheumatology
Volume44
Numéro de publication12
DOI
Statut de publicationPublished - déc. 1 2017

Note bibliographique

Publisher Copyright:
Copyright © 2017. All rights reserved.

ASJC Scopus Subject Areas

  • Immunology and Allergy
  • Rheumatology
  • Immunology

PubMed: MeSH publication types

  • Journal Article

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