Immunological biomarkers predict pulmonary and nodal, but not cardiac PET-assessed sarcoidosis activity

Background Sarcoidosis is a systemic granulomatous disease with highly variable clinical manifestations and organ involvement. Symptoms are often unspecific or absent and may not reflect true inflammatory burden, increasing the risk of delayed detection of organ damage. Reliable assessment of disease activity is therefore essential for treatment guidance. We aimed to investigate the correlation and predictive performance of circulating biomarkers with systemic inflammatory activity as assessed by 18 F-FDG PET-CT, exploring whether a biomarker-based approach could substitute more resource-intensive imaging. Methods We conducted a retrospective cohort study including 180 patients with systemic sarcoidosis who underwent paired 18 F-FDG PET-CT and blood sampling (N=770). Systemic biomarkers including TNFα, sIL-2R, neopterin, ACE activity, CRP, calciuria, and lymphocytopenia were assessed for their association with PET-based inflammatory activity. Variance and correlation analyses as well as ROC curves were used to evaluate diagnostic performance. Results TNFα, sIL-2R, and neopterin consistently showed significant correlation with PET activity already for moderate inflammatory activity (activity-quartile 2–3 versus inactive: p<0.001), with TNFα showing the best predictive ability, though overall degree of correlation remained moderate (Pearson's r<0.5; AUCs: 0.63–0.68). Traditional biomarkers such as ACE activity and CRP only showed significant differences at the highest quartile of PET activity (activity-quartile 4 versus inactive: p<0.001 and p=0.005, respectively). While biomarker correlations were evident for pulmonary and nodal inflammation, weak to no association was found for PET-assessed cardiac activity. Conclusion Immunological biomarkers such as TNFα, sIL-2R and Neopterin outperform traditional markers such as CRP and ACE activity, and should be considered in the assessment of systemic sarcoidosis activity at diagnosis and follow up. Since no biomarker was able to predict cardiac inflammatory activity, imaging techniques such as MRI and 18 F-FDG PET remain central for diagnosis and exclusion of cardiac sarcoidosis.

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Journal
ERJ Open Research
Published
2026-04-16
DOI
https://doi.org/10.1183/23120541.01414-2025
Primary Topic
Sarcoidosis and Beryllium Toxicity Research
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article
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article

Immunological biomarkers predict pulmonary and nodal, but not cardiac PET-assessed sarcoidosis activity

R Colli, Lukas Frischknecht, Ronny R. Buechel, Jakob Nilsson et al.
ERJ Open Research
Sarcoidosis and Beryllium Toxicity Research
article

Immunological biomarkers predict pulmonary and nodal, but not cardiac PET-assessed sarcoidosis activity

R Colli, Lukas Frischknecht, Ronny R. Buechel, Jakob Nilsson, Sonja Katz, Melina Stuessi-Helbling, Christian Clarenbach, Yuan Tian, Anna Himmelmann-Wildschuetz
article en

Abstract

Background Sarcoidosis is a systemic granulomatous disease with highly variable clinical manifestations and organ involvement. Symptoms are often unspecific or absent and may not reflect true inflammatory burden, increasing the risk of delayed detection of organ damage. Reliable assessment of disease activity is therefore essential for treatment guidance. We aimed to investigate the correlation and predictive performance of circulating biomarkers with systemic inflammatory activity as assessed by 18 F-FDG PET-CT, exploring whether a biomarker-based approach could substitute more resource-intensive imaging. Methods We conducted a retrospective cohort study including 180 patients with systemic sarcoidosis who underwent paired 18 F-FDG PET-CT and blood sampling (N=770). Systemic biomarkers including TNFα, sIL-2R, neopterin, ACE activity, CRP, calciuria, and lymphocytopenia were assessed for their association with PET-based inflammatory activity. Variance and correlation analyses as well as ROC curves were used to evaluate diagnostic performance. Results TNFα, sIL-2R, and neopterin consistently showed significant correlation with PET activity already for moderate inflammatory activity (activity-quartile 2–3 versus inactive: p<0.001), with TNFα showing the best predictive ability, though overall degree of correlation remained moderate (Pearson's r<0.5; AUCs: 0.63–0.68). Traditional biomarkers such as ACE activity and CRP only showed significant differences at the highest quartile of PET activity (activity-quartile 4 versus inactive: p<0.001 and p=0.005, respectively). While biomarker correlations were evident for pulmonary and nodal inflammation, weak to no association was found for PET-assessed cardiac activity. Conclusion Immunological biomarkers such as TNFα, sIL-2R and Neopterin outperform traditional markers such as CRP and ACE activity, and should be considered in the assessment of systemic sarcoidosis activity at diagnosis and follow up. Since no biomarker was able to predict cardiac inflammatory activity, imaging techniques such as MRI and 18 F-FDG PET remain central for diagnosis and exclusion of cardiac sarcoidosis.

ERJ Open Research
University of Zurich (CH), University Hospital of Zurich (CH)
Openalex Percentile: Top 19%
Sarcoidosis and Beryllium Toxicity Research
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