Role of Osteopontin as a Potential Biomarker of Pulmonary Arterial Hypertension in Patients with Systemic Sclerosis and Other Connective Tissue Diseases (CTDs)
- PMID: 33919476
- PMCID: PMC8143460
- DOI: 10.3390/ph14050394
Role of Osteopontin as a Potential Biomarker of Pulmonary Arterial Hypertension in Patients with Systemic Sclerosis and Other Connective Tissue Diseases (CTDs)
Abstract
Pulmonary arterial hypertension (PAH) is a severe complication of connective tissue diseases (CTD). Its early diagnosis is essential to start effective treatment. In the present paper, we aimed to evaluate the role of plasma osteopontin (OPN) as a candidate biomarker of PAH in a cohort of CTD patients. OPN is a pleiotropic protein involved in inflammation and fibrogenesis and, therefore, potentially promising in this specific clinical context. We performed a cross-sectional observational study on a cohort of 113 CTD patients (females N = 101, 89.4%) affected by systemic sclerosis N = 88 (77.9%), mixed connective tissue disease N = 10 (8.8%), overlap syndrome N = 10 (8.8%) or undifferentiated connective tissue disease N = 5 (4.4%). CTD-PAH patients showed significantly higher OPN plasma values than patients with CTD alone (241.0 (188.8-387.2) vs. 200.7 (133.5-281.6) ng/mL; p = 0.03). Although OPN levels were directly correlated with age and inversely with glomerular filtration rate, they remained associated with PAH at multivariate analysis. In conclusion, OPN was significantly associated with PAH among patients with CTD, suggesting it may have a role as a non-invasive disease biomarker of PAH.
Keywords: connective tissue diseases; osteopontin; pulmonary arterial hypertension; systemic sclerosis.
Conflict of interest statement
The authors declare no conflict of interest.
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References
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- Galiè N., Humbert M., Vachiery J.L., Gibbs S., Lang I., Torbicki A., Simonneau G., Peacock A., Vonk Noordegraaf A., Beghetti M., et al. ESC Scientific Document Group. 2015 ESC/ERS Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension. Eur. Heart J. 2016;37:67–119. doi: 10.1093/eurheartj/ehv317. - DOI - PubMed
-
- Ruiz-Cano M.J., Escribano P., Alonso R., Delgado J., Carreira P., Velazquez T., Sanchez M.A.G., de la Calzada C.S. Comparison of Baseline Characteristics and Survival between Patients with Idiopathic and Connective Tissue Disease–related Pulmonary Arterial Hypertension. J. Heart Lung Transplant. 2009;28:621–627. doi: 10.1016/j.healun.2009.02.016. - DOI - PubMed
-
- Coghlan J.G., Denton C.P., Grünig E., Bonderman D., Distler O., Khanna D., Müller-Ladner U., Pope J.E., Vonk M.C., Doelberg M., et al. Evidence-Based Detection of Pulmonary Arterial Hypertension in Systemic Sclerosis: The DETECT Study. Ann. Rheum. Dis. 2014;73:1340–1349. doi: 10.1136/annrheumdis-2013-203301. - DOI - PMC - PubMed
-
- Bellan M., Dimagli A., Piccinino C., Giubertoni A., Ianniello A., Grimoldi F., Sguazzotti M., Nerviani A., Barini M., Carriero A., et al. Role of Gas6 and TAM Receptors in the Identification of Cardiopulmonary Involvement in Systemic Sclerosis and Scleroderma Spectrum Disorders. Dis. Markers. 2020:2696173. doi: 10.1155/2020/2696173. - DOI - PMC - PubMed
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