Imaging pulmonary inflammation with positron emission tomography: A biomarker for drug development

Delphine L. Chen, Daniel P. Schuster

Research output: Contribution to journalReview article

38 Scopus citations

Abstract

Methods currently used to assess lung and airway inflammation are often poorly quantitative, invasive, nonspecific, or insensitive. Positron emission tomography (PET) with [18F]-fluorodeoxyglucose ([18F]FDG), on the other hand, is a noninvasive, highly sensitive imaging technique that can be used to quantify pulmonary inflammation. [18F]FDG, an analogue of glucose, is taken up by the same transporters that take up glucose into the cell; therefore, [18F]-FDG uptake tracks cellular glucose transport, which is highly correlated to the rate of cellular glucose metabolism. Recent studies in animal models of neutrophilic lung inflammation, as well as in patients with inflammatory lung disease, indicate that increased [ 18F]FDG uptake by the lungs correlates with the number of activated neutrophils recovered from the lungs. Therefore, the in vivo measurement of pulmonary glucose metabolism is a measure of neutrophil burden within the lungs. We propose that FDG-PET imaging can be used as a measurable biomarker in the development of drug therapies targeting lung inflammation.

Original languageEnglish
Pages (from-to)488-495
Number of pages8
JournalMolecular Pharmaceutics
Volume3
Issue number5
DOIs
StatePublished - Sep 1 2006

Keywords

  • Drug evaluation
  • Fluorodeoxyglucose
  • Lung inflammation
  • Positron emission tomography
  • Preclinical drug evaluation

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