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(18)F-FDG positron emission tomography scanning in systemic sclerosis-associated interstitial lung disease: a pilot study

BACKGROUND: Interstitial lung disease is a common complication of systemic sclerosis (SSc-ILD), and it remains difficult to accurately predict its course. Progressing ILD could be more metabolically active, suggesting that the (18)F-FDG tracer could be a tool in the managing of SSc-ILD. METHODS: In...

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Detalles Bibliográficos
Autores principales: Ledoult, Emmanuel, Morelle, Maxime, Soussan, Michael, Mékinian, Arsène, Béhal, Hélène, Sobanski, Vincent, Hachulla, Eric, Huglo, Damien, Le Gouellec, Noémie, Remy-Jardin, Martine, Baillet, Clio, Launay, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936499/
https://www.ncbi.nlm.nih.gov/pubmed/33673861
http://dx.doi.org/10.1186/s13075-021-02460-8
Descripción
Sumario:BACKGROUND: Interstitial lung disease is a common complication of systemic sclerosis (SSc-ILD), and it remains difficult to accurately predict its course. Progressing ILD could be more metabolically active, suggesting that the (18)F-FDG tracer could be a tool in the managing of SSc-ILD. METHODS: In our center, SSc patients and controls (non-Hodgkin lymphoma cured after first-line regimen) who had received a PET/CT were screened retrospectively. The FDG uptake (visual intensity, pattern, SUV(max)) was systematically recorded in > 30 regions of interest (ROIs) linked to SSc in a blind reviewing by 2 independent nuclear medicine physicians using a standardized form. RESULTS: Among the 545 SSc patients followed up in our center, 36, including 22 SSc-ILDs, had a PET/CT, whose indication was cancer screening in most cases. The mean ± SD age was 57.9 ± 13.0 years with 20/36 females. Fourteen patients had a disease duration of less than 2 years. A third had anti-centromere antibodies and 27.8% had anti-topoisomerase antibodies. Pulmonary FDG uptakes were higher in SSc patients than in controls (n = 89), especially in those with ILD compared with those without ILD. Pulmonary FDG uptakes were positively correlated with the ILD severity (fibrosis extent, %FVC, and %D(LCO)). No significant difference was found in the FDG uptakes from extrathoracic ROIs. Progressing SSc-ILDs within the 2 years after PET/CT (n = 9) had significant higher pulmonary FDG uptakes at baseline than stable SSc-ILDs (n = 13). CONCLUSION: PET/CT could be a useful tool in the assessment of the severity and the prediction of pulmonary function outcome of SSc-ILD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-021-02460-8.