Purpose
The potential to use FDG PET/CT in diffuse lung diseases is becoming increasingly recognised. To understand the potential of the technique better, we investigated the correlation between [18F]FDG lung uptake with microvessel density (MVD) on lung biopsy of patients with fibrotic interstitial lung disease (fILD).
Methods
We recruited 18 patients with fILD who underwent [18F]FDG PET before lung biopsy. We derived target-to-background ratio (TBR) of maximum pulmonary uptake of FDG (SUVmax) divided by the lung background (SUVmin). Consecutive paraffin-embedded sections obtained from biopsy were immunostained for alveolar and interstitial macrophages (CD68), microvessel density (MVD; CD31 and CD105/ endoglin) and glucose transporter 1 (GLUT-1). MVD was expressed as vessel area % per high-power field (Va%/hpf); Statistical analysis was carried out using SPSS.
Results
18 patients were followed for an average of 41.36 months (range 5.69-132.46 months; median 30.07 months). In all patients, MVD assessed with either CD105 or CD31 quantification on biopsy predicted overall survival. Patients with low CD105-MVD (score of < 12 Va%/hpf) and/or low CD31-MVD (score of < 34 Va%/hpf) had a significantly better prognosis (no deaths during follow-up) than patients with higher scores of CD105-MVD (median survival < 35 months, p = 0.041, n = 13) or CD31-MVD (median survival < 30 months, p = 0.037, n = 13). However, only CD105-MVD showed a significantly positive correlation with [18F]FDG TBR (rs = 0.556, p < 0.05, n = 13). There was no correlation between [18F]FDG uptake and macrophage expression of GLUT-1.
Conclusion
Previous work has used FDG-PET as a biomarker in fILD. Here we highlight a correlation between angiogenesis and FDG TBR, both of which predict mortality in patients with fILD. These data set the scene to investigate the potential role of the vasculature and angiogenesis in fibrosis.