期刊论文详细信息
Journal of Nuclear Medicine
18F-FDG Uptake Rate Is a Biomarker of Eosinophilic Inflammation and Airway Response in Asthma
Josalyn Cho1  Marcos F. Vidal Melo1  Chanikarn Wongviriyawong1  José G. Venegas1  R. Scott Harris1  Roshi Afshar1  Daniel L. Hamilos1  Benjamin D. Medoff1  Tilo Winkler1  Nicolas de Prost1  Mamary Kone1  Andrew D. Luster1  Guido Musch1 
关键词: airway constriction;    ventilation–perfusion ratio;    pulmonary gas exchange;    fluorine isotopes;    emission-computed tomography;    nitrogen isotopes;   
DOI  :  10.2967/jnumed.110.086355
学科分类:医学(综合)
来源: Society of Nuclear Medicine
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【 摘 要 】

In asthma, the relationship among airway inflammation, airway hyperresponsiveness, and lung function is poorly understood. Methods to noninvasively assess these relationships in human subjects are needed. We sought to determine whether 18F-FDG uptake rate (Ki, min−1) could serve as a biomarker of eosinophilic inflammation and local lung function. Methods: We used PET/CT to assess regional pulmonary perfusion (), specific ventilation per unit volume (), fractional gas content (Fgas), airway wall thickness, and regional Ki 10 h after segmental allergen challenge to the right middle lobe in 6 asthmatic subjects with demonstrated atopy. , , and Fgas in the allergen-challenged lobe were compared with the right upper lobe, where diluent was applied as a control. The airway wall thickness aspect ratio (ω) of the allergen-challenged airway was compared with those of similarly sized airways from unaffected areas of the lung. Differences in Ki between allergen and diluent segments were compared with those in cell counts obtained 24 h after the allergen challenge by a bronchoalveolar lavage of the respective segments. Results: We found systematic reductions in regional , , and Fgas and increased ω in all subjects. The ratio of eosinophil count (allergen to diluent) was linearly related (R2 = 0.9917, P < 0.001) to the ratio of Ki. Conclusion: Regional Ki measured with PET is a noninvasive and highly predictive biomarker of eosinophilic airway inflammation and its functional effects. This method may serve to help in the understanding of allergic inflammation and test the therapeutic effectiveness of novel drugs or treatments.

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