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Role of Gas6 and TAM Receptors in the Identification of Cardiopulmonary Involvement in Systemic Sclerosis and Scleroderma Spectrum Disorders

Background. Few biomarkers are available for early identification of pulmonary arterial hypertension (PAH) and interstitial lung disease (ILD) in systemic sclerosis (SS) and scleroderma spectrum disorders (SSD). Aims. To evaluate Gas6, sAxl, and sMer as biomarkers for cardiopulmonary complications o...

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Published in:Disease markers 2020, Vol.2020, p.2696173-8
Main Authors: Bellan, Mattia, Dimagli, Arnaldo, Piccinino, Cristina, Giubertoni, Ailia, Ianniello, Aurora, Grimoldi, Federico, Sguazzotti, Maurizio, Nerviani, Alessandra, Barini, Michela, Carriero, Alessandro, Smirne, Carlo, Burlone, Michela Emma, Rigamonti, Cristina, Minisini, Rosalba, Salmi, Livia, Barbaglia, Matteo Nazzareno, Castello, Luigi Mario, Sola, Daniele, Marino, Paolo, Avanzi, Gian Carlo, Pirisi, Mario, Sainaghi, Pier Paolo
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Language:English
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Summary:Background. Few biomarkers are available for early identification of pulmonary arterial hypertension (PAH) and interstitial lung disease (ILD) in systemic sclerosis (SS) and scleroderma spectrum disorders (SSD). Aims. To evaluate Gas6, sAxl, and sMer as biomarkers for cardiopulmonary complications of SS and SSD. Methods. In a cross-sectional observational study, we recruited 125 consecutive patients, affected by SS and SSD and referred to a tertiary-level pulmonary hypertension outpatient clinic. All patients underwent a comprehensive evaluation for identification of PAH and ILD. Gas6, sMer, and sAxl concentrations were measured with ELISA protocols, and concentrations were compared according to PAH or ILD. Results. Nineteen subjects had pulmonary hypertension (PH) (14 PAH), and 39 had ILD (6 severe). Plasma sMer was increased in PAH (18.6 ng/ml IQR [11.7-20.3]) with respect to the absence (12.4 [8.0-15.8]) or other form of pulmonary hypertension (9.6 [7.4-12.5]; K–W variance p
ISSN:0278-0240
1875-8630
DOI:10.1155/2020/2696173