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Updated: Jul 10, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Positron emission tomography in interstitial lung disease
Samir Nusair1, Rina Rubinstein, Nanette M Freedman
1The Institute of Pulmonology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel. samjack@shani.net
Positron emission tomography (PET) scans using 18FDG did not differentiate idiopathic pulmonary fibrosis (IPF) from other interstitial lung diseases (ILDs) with inflammatory components. Further research is needed to distinguish these conditions effectively.
Area of Science:
- Pulmonary Medicine
- Nuclear Medicine
- Radiology
Background:
- Glycolysis rates may indicate inflammation in interstitial lung disease (ILD).
- Idiopathic pulmonary fibrosis (IPF) is primarily fibrotic, unlike some ILDs with significant inflammation.
Purpose of the Study:
- To determine if Positron Emission Tomography (PET) can differentiate IPF from other ILDs based on inflammatory activity.
- To investigate the utility of 18FDG PET in distinguishing fibrotic ILD from inflammatory ILD.
Main Methods:
- Prospective study of 21 patients with diffuse ILD undergoing surgical lung biopsy.
- 18FDG PET scans were performed, and standardized uptake values (SUV) were calculated for lung regions of interest.
- Comparison of SUV between IPF and non-IPF patients.
Main Results:
- No statistically significant difference in SUV was found between IPF and non-IPF patients (P=0.26).
- IPF patients showed a trend towards higher SUV, but this was not statistically significant.
- No significant difference in the SUV ratio between upper and whole lungs was observed between IPF and non-IPF groups (P=0.31).
Conclusions:
- PET imaging with 18FDG does not reliably differentiate IPF from other diffuse interstitial pulmonary processes.
- The inflammatory component of ILD, as assessed by 18FDG uptake, does not distinguish IPF from non-IPF conditions.
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