Evidence map›Paper›PMID 41024250›Full record

ArticleArthritis research & therapy2025

Longitudinal assessment of circulating fibroblast activation protein in systemic sclerosis-associated interstitial lung disease.

Bo Broens, Conny J van der Laken, Iris A Simons, Tamara Dekker, Jan-Willem Duitman, Alexandre E Voskuyl

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Article in Arthritis research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Bo BroensDepartment of Rheumatology and Clinical Immunology, Amsterdam UMC, Amsterdam, The Netherlands.
Conny J van der LakenDepartment of Rheumatology and Clinical Immunology, Amsterdam UMC, Amsterdam, The Netherlands.
Iris A SimonsDepartment of Pulmonary Medicine, Amsterdam UMC, Amsterdam, The Netherlands.
Tamara DekkerDepartment of Pulmonary Medicine, Amsterdam UMC, Amsterdam, The Netherlands.
Jan-Willem DuitmanDepartment of Pulmonary Medicine, Amsterdam UMC, Amsterdam, The Netherlands.
Alexandre E VoskuylDepartment of Rheumatology and Clinical Immunology, Amsterdam UMC, Amsterdam, The Netherlands. ae.voskuyl@amsterdamumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic sclerosis-associated interstitial lung disease (SSc-ILD) is difficult to manage due to the heterogeneous disease course. There is a high need for new biomarkers to identify patients at high risk for ILD progression. Fibroblast activation protein (FAP) has gained interest as a biomarker to reflect fibrotic activity. As circulating FAP (cFAP) can be measured in blood, we aimed to investigate the value of cFAP in SSc-ILD.

methodscFAP concentrations were determined in plasma samples of 210 patients with systemic sclerosis (SSc) using an enzyme-linked immunosorbent assay. We compared cFAP in baseline and repeated longitudinal samples between SSc patients with (n = 63) and without ILD (n = 147). Furthermore, we investigated the correlation between cFAP and ILD progression at follow-up. In an exploratory analysis, we also investigated if cFAP was associated with other disease-related clinical features and all-cause mortality.

resultscFAP levels were not different between SSc patients with- and without ILD, both at baseline (median 91.5 and 97.7 ng/mL respectively; p = 0.80) or during follow-up. Furthermore, we found no association between cFAP at baseline and ILD progression at 1, 2 and 5 years of follow-up. Notably, cFAP levels were elevated at baseline in patients with higher skin scores (mRSS ≥ 10 compared to mRSS < 10; p = 0.01). Finally, we did not find an association between cFAP and all-cause mortality at 5 and 10 years of follow-up.

conclusionIn conclusion, cFAP does not seem useful as a biomarker in SSc-ILD. However, the association between cFAP and skin score deserves further investigation.

Indexed as

GelatinasesLung Diseases, InterstitialMembrane ProteinsScleroderma, SystemicSerine EndopeptidasesAdultAgedBiomarkersDisease ProgressionEndopeptidasesFemaleFibroblast Activation Protein AlphaHumansLongitudinal StudiesMaleMiddle AgedBiomarkersEndopeptidasesFibroblast Activation Protein AlphaGelatinasesMembrane ProteinsSerine EndopeptidasesBiomarkerFibroblast activation proteinInterstitial lung diseaseSystemic sclerosis

Identifiers

PMID41024250
PMCPMC12482540

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