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Article

Serum Biomarkers in Differential Diagnosis of Idiopathic Pulmonary Fibrosis and Connective Tissue Disease-Associated Interstitial Lung Disease

1
Respiratory Service, Universitary Virgen de la Victoria Hospital, 29010 Málaga, Spain
2
Department of Physiology and Human Histology, Faculty of Medicine, University of Málaga, Biomedical Research Institute of Málaga, 29010 Málaga, Spain
3
Department of Biochemistry, Biomedical Research Institute of Málaga, Faculty of Medicine, University of Málaga, 29010 Málaga, Spain
4
Department of Pharmacology and Paediatrics, Faculty of Medicine, University of Málaga, Biomedical Research Institute of Málaga, 29010 Málaga, Spain
*
Author to whom correspondence should be addressed.
These authors have contributed equally to the present work.
Academic Editor: Yan Sanders
J. Clin. Med. 2021, 10(14), 3167; https://doi.org/10.3390/jcm10143167
Received: 27 June 2021 / Revised: 13 July 2021 / Accepted: 15 July 2021 / Published: 18 July 2021
(This article belongs to the Section Pulmonology)
Introduction: The goal of this study is to determine whether Advanced glycosylated end-products (AGE), Advanced oxidation protein products (AOPP) and Matrix metalloproteinase 7 (MMP7) could be used as differential biomarkers for idiopathic pulmonary fibrosis (IPF) and connective tissue disease-associated interstitial lung disease (CTD-ILD). Method: Seventy-three patients were enrolled: 29 with IPF, 14 with CTD-ILD, and 30 healthy controls. The study included a single visit by participants. A blood sample was drawn and serum was analysed for AGE using spectrofluorimetry, AOPP by spectrophotometry, and MMP7 using sandwich-type enzyme-linked immunosorbent assay. Results: AGE, AOPP and MMP7 serum levels were significantly higher in both IPF and CTD-ILD patients versus healthy controls; and AGE was also significantly elevated in CTD-ILD compared to the IPF group. AGE plasma levels clearly distinguished CTD-ILD patients from healthy participants (AUC = 0.95; 95% IC 0.86–1), whereas in IPF patients, the distinction was moderate (AUC = 0.78; 95% IC 0.60–0.97). Conclusion: In summary, our results provide support for the potential value of serum AGE, AOPP and MMP7 concentrations as diagnostic biomarkers in IPF and CTD-ILD to differentiate between ILD patients and healthy controls. Furthermore, this study provides evidence, for the first time, for the possible use of AGE as a differential diagnostic biomarker to distinguish between IPF and CTD-ILD. The value of these biomarkers as additional tools in a multidisciplinary approach to IPF and CTD-ILD diagnosis needs to be considered and further explored. Multicentre studies are necessary to understand the role of AGE in differential diagnosis. View Full-Text
Keywords: IPF; progressive pulmonary fibrosis; biomarkers IPF; progressive pulmonary fibrosis; biomarkers
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MDPI and ACS Style

Cabrera Cesar, E.; Lopez-Lopez, L.; Lara, E.; Hidalgo-San Juan, M.V.; Parrado Romero, C.; Palencia, J.L.R.S.; Martín-Montañez, E.; Garcia-Fernandez, M. Serum Biomarkers in Differential Diagnosis of Idiopathic Pulmonary Fibrosis and Connective Tissue Disease-Associated Interstitial Lung Disease. J. Clin. Med. 2021, 10, 3167. https://doi.org/10.3390/jcm10143167

AMA Style

Cabrera Cesar E, Lopez-Lopez L, Lara E, Hidalgo-San Juan MV, Parrado Romero C, Palencia JLRS, Martín-Montañez E, Garcia-Fernandez M. Serum Biomarkers in Differential Diagnosis of Idiopathic Pulmonary Fibrosis and Connective Tissue Disease-Associated Interstitial Lung Disease. Journal of Clinical Medicine. 2021; 10(14):3167. https://doi.org/10.3390/jcm10143167

Chicago/Turabian Style

Cabrera Cesar, Eva, Lidia Lopez-Lopez, Estrella Lara, M. V. Hidalgo-San Juan, Concepcion Parrado Romero, Jose L.R.S. Palencia, Elisa Martín-Montañez, and Maria Garcia-Fernandez. 2021. "Serum Biomarkers in Differential Diagnosis of Idiopathic Pulmonary Fibrosis and Connective Tissue Disease-Associated Interstitial Lung Disease" Journal of Clinical Medicine 10, no. 14: 3167. https://doi.org/10.3390/jcm10143167

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