Your browser doesn't support javascript.
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
1.
Int J Biol Sci ; 17(6): 1565-1573, 2021.
Artículo en Inglés | MEDLINE | ID: covidwho-1206427

RESUMEN

Dysregulated immune response and abnormal repairment could cause secondary pulmonary fibrosis of varying severity in COVID-19, especially for the elders. The Krebs Von den Lungen-6 (KL-6) as a sensitive marker reflects the degree of fibrosis and this study will focus on analyzing the evaluative efficacy and predictive role of KL-6 in COVID-19 secondary pulmonary fibrosis. The study lasted more than three months and included total 289 COVID-19 patients who were divided into moderate (n=226) and severe groups (n=63) according to the severity of illness. Clinical information such as inflammation indicators, radiological results and lung function tests were collected. The time points of nucleic acid test were also recorded. Furthermore, based on Chest radiology detection, it was identified that 80 (27.7%) patients developed reversible pulmonary fibrosis and 34 (11.8%) patients developed irreversible pulmonary fibrosis. Receiver operating characteristic (ROC) curve analysis shows that KL-6 could diagnose the severity of COVID-19 (AUC=0.862) and predict the occurrence of pulmonary fibrosis (AUC = 0.741) and irreversible pulmonary fibrosis (AUC=0.872). Importantly, the cross-correlation analysis demonstrates that KL-6 rises earlier than the development of lung radiology fibrosis, thus also illuminating the predictive function of KL-6. We set specific values (505U/mL and 674U/mL) for KL-6 in order to assess the risk of pulmonary fibrosis after SARS-CoV-2 infection. The survival curves for days in hospital show that the higher the KL-6 levels, the longer the hospital stay (P<0.0001). In conclusion, KL-6 could be used as an important predictor to evaluate the secondary pulmonary fibrosis degree for COVID-19.


Asunto(s)
COVID-19/complicaciones , Mucina-1/metabolismo , Fibrosis Pulmonar/complicaciones , Adulto , Anciano , COVID-19/virología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Fibrosis Pulmonar/terapia , Factores de Riesgo , SARS-CoV-2/aislamiento & purificación
2.
J Med Virol ; 93(3): 1443-1448, 2021 03.
Artículo en Inglés | MEDLINE | ID: covidwho-1196454

RESUMEN

Our study intended to longitudinally explore the prediction effect of immunoglobulin A (IgA) on pulmonary exudation progression in COVID-19 patients. The serum IgA was tested with chemiluminescence method. Autoregressive moving average model was used to extrapolate the IgA levels before hospital admission. The positive rate of IgA and IgG in our cohort was 97% and 79.0%, respectively. In this study, the IgA levels peaks within 10-15 days after admission, while the IgG levels peaks at admission. We found that the time difference between their peaks was about 10 days. Viral RNA detection results showed that the positive rate in sputum and feces were the highest. Blood gas analysis showed that deterioration of hypoxia with the enlargement of pulmonary exudation area. And alveolar-arterial oxygen difference and oxygenation index were correlated with IgA and IgG. The results of biopsy showed that the epithelium of lung was exfoliated and the mucosa was edematous. In severe COVID-19 patients, the combination of IgA and IgG can predict the progress of pulmonary lesions and is closely related to hypoxemia and both also play an important defense role in invasion and destruction of bronchial and alveolar epithelium by SARS-CoV-2.


Asunto(s)
COVID-19/patología , COVID-19/virología , Inmunoglobulina A/sangre , Inmunoglobulina G/sangre , Esputo/virología , Anciano , Células Epiteliales Alveolares/metabolismo , Células Epiteliales Alveolares/virología , Anticuerpos Antivirales/sangre , Bronquios/metabolismo , Bronquios/virología , COVID-19/sangre , COVID-19/metabolismo , Femenino , Humanos , Hipoxia/sangre , Hipoxia/metabolismo , Masculino , Persona de Mediana Edad , Membrana Mucosa/metabolismo , Membrana Mucosa/virología , Oxígeno/metabolismo , Alveolos Pulmonares/metabolismo , Alveolos Pulmonares/virología , ARN Viral/genética , SARS-CoV-2/genética
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA