The Role of Serum Prolidase Activity, MMP-1, MMP-7, and TGF-β Values in the Prediction of Early Fibrosis in Patients with Moderate to Severe COVID-19.

Publication date: Jul 06, 2025

This study aims to identify predictive factors for pulmonary fibrosis development in COVID-19 patients by analyzing thorax CT (computed tomography) findings, serum prolidase activity, MMP-1, MMP-7, TGF-β values, laboratory findings, and demographic characteristics. The investigation involved 68 patients, both male and female, aged 18 years and older, who were volunteers and had been diagnosed with confirmed COVID-19. The pulmonologist and the radiologist evaluated the thorax CT by consensus. Patients were evaluated in two categories, group 1 and group 2, based on the status of fibrotic changes, and 3-month fibrosis scores were calculated. Findings in both lungs were calculated and noted for the lobes, considering lobar spread. Correlations between quantitative parameters were assessed with Spearman’s rho correlation coefficient. Comparisons between independent samples were evaluated using either the independent sample t-test or the Mann-Whitney U test. We evaluated the relationship between categorical variables using the Pearson chi-square test and Fisher’s exact test. Serum prolidase activity, MMP-1, MMP-7, and TGF-β biomarkers were not statistically significant among groups. LDH was found to be significantly high in the group with fibrotic changes. Additionally, the group with fibrotic changes also had higher levels of fibrinogen. The percentage of neutrophils, the severity of the disease, muscle-joint pain and fatigue symptoms, and the length of hospitalization stay were correlated with the total scores of fibrosis at the third month. In the group with fibrotic changes, the duration of muscle-joint pain and fatigue symptoms and the length of hospitalization were longer than in the other group. The group with fibrotic changes showed an increase in biomarkers. However, this increase did not reach a statistically significant level, suggesting that the third month may be an early period for these changes. The group with fibrotic changes showed high levels of LDH, one of the most important laboratory parameters of pulmonary fibrosis risk factors, along with fibrinogen, suggesting that these parameters are valuable in predicting pulmonary fibrosis. Patients with fibrotic changes can experience specific symptoms, commonly seen in COVID-19.

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Concepts Keywords
Genes Adult
Hospitalization Aged
Pulmonary Biomarkers
Spearman Biomarkers
Tomography COVID-19
Dipeptidases
Dipeptidases
Female
Humans
LDH
Lung
Male
Matrix Metalloproteinase 1
Matrix Metalloproteinase 1
Matrix Metalloproteinase 7
Matrix Metalloproteinase 7
Middle Aged
MMP-1
MMP-7
MMP1 protein, human
MMP7 protein, human
post-COVID-19
proline dipeptidase
Pulmonary Fibrosis
SARS-CoV-2
serum prolidase activity
TGF-β
Tomography, X-Ray Computed

Semantics

Type Source Name
disease IDO role
disease MESH Fibrosis
disease MESH COVID-19
disease MESH pulmonary fibrosis
drug DRUGBANK Fibrinogen Human
disease MESH joint pain
drug DRUGBANK Coenzyme M
disease MESH Pneumonia
pathway KEGG Coronavirus disease
disease MESH Emergency
disease MESH infection
disease MESH Middle East Respiratory Syndrome
disease IDO blood
disease MESH idiopathic pulmonary fibrosis
disease MESH Lymphopenia
disease MESH lung injury
disease MESH Thrombocytopenia
disease MESH Acute Respiratory Distress Syndrome
drug DRUGBANK Iron
drug DRUGBANK Spinosad
disease MESH inflammation
disease MESH viral infection
disease MESH drug toxicity
disease IDO immune response
drug DRUGBANK Urea
disease MESH malignancy
disease MESH bronchiectasis
drug DRUGBANK Albendazole
drug DRUGBANK Oxygen
disease MESH Comorbidity
disease MESH pulmonary diseases
disease MESH Dyspnea
disease MESH Sore throat
disease MESH Chest pain
drug DRUGBANK Medical air
disease MESH Asthma
pathway KEGG Asthma
disease MESH chronic obstructive pulmonary disease
disease MESH hypertension
disease MESH diabetes mellitus
disease MESH coronary artery disease
disease MESH hyperlipidemia
disease MESH congestive heart failure

Original Article

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