18F-NaF PET/CT identifies muscular and subcutaneous calcifications in both dermatomyositis- and systemic sclerosis-related calcinosis
BackgroundCalcinosis is a morbid complication of dermatomyositis (DM) and systemic sclerosis (SSc) with no effective pharmacologic treatment or validated whole-body assessment modality. 18F-NaF PET/CT may help to quantify and characterize calcinosis.MethodsIn this pilot study, we enrolled three adul...
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| Main Authors: | , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2025-05-01
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| Series: | Frontiers in Nuclear Medicine |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fnume.2025.1593825/full |
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| Summary: | BackgroundCalcinosis is a morbid complication of dermatomyositis (DM) and systemic sclerosis (SSc) with no effective pharmacologic treatment or validated whole-body assessment modality. 18F-NaF PET/CT may help to quantify and characterize calcinosis.MethodsIn this pilot study, we enrolled three adults with DM and three with SSc, all with new calcinosis deposits. Each underwent 18F-NaF PET/CT and clinical examination with semi-quantitative scoring of calcinosis. We described the 18F-NaF PET/CT findings and compared these to CT imaging alone as well as to clinical examination.ResultsCalcinosis was noted on 18F-NaF PET/CT in the subcutaneous tissue in all patients and the muscle in three patients, including two with SSc. The average semi-quantitative score was 23.5 by 18F-NaF PET/CT and 20 by clinical exam. Wilcoxon signed rank test indicated greater scores by 18F-NaF PET/CT than by clinical exam (p = 0.0264). 18F-NaF uptake varied among calcinosis deposits and occurred without corresponding calcifications on CT.Conclusions18F-NaF PET/CT appears to be a sensitive method of detecting and characterizing calcinosis that provides both quantitative and qualitative data beyond what can be obtained by physical examination or CT alone. 18F-NaF uptake occurs in muscle in both SSc and DM, suggesting the possibility that myositis may be driving calcinosis in a subset of patients with SSc. |
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| ISSN: | 2673-8880 |