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Krebs von den Lungen-6 levels in untreated idiopathic pulmonary fibrosis.
Jiang, Dingyuan; Xiao, Huijuan; Dong, Run; Geng, Jing; Xie, Bingbing; Ren, Yanhong; Dai, Huaping.
Afiliación
  • Jiang D; Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Beijing, China.
  • Xiao H; Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Beijing, China.
  • Dong R; Department of Respiratory Medicine, Capital Medical University, Beijing, China.
  • Geng J; Department of Respiratory Medicine, Zhengzhou Central Hospital, Zhengzhou, China.
  • Xie B; Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Beijing, China.
  • Ren Y; Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Beijing, China.
  • Dai H; Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Beijing, China.
Clin Respir J ; 16(3): 234-243, 2022 Mar.
Article en En | MEDLINE | ID: mdl-35081277
BACKGROUND: Serum Krebs von den Lungen-6 (KL-6) has been reported to be elevated in patients with idiopathic pulmonary fibrosis (IPF). OBJECTIVE: The aim of this study was to evaluate the diagnostic value of KL-6 and whether the expression value of KL-6 could indicate the severity of the disease in IPF patients. To address this question, it is necessary to see whether the patients' physical characteristics and other clinical conditions could affect the baseline KL-6 level. DESIGN: We conducted a study of 100 patients who were diagnosed with IPF. Lung function, computed tomography (CT), and serological lab tests data were analyzed. RESULTS: The tests showed that there is a significant elevation of KL-6 in IPF patients compared with other interstitial lung disease (ILD) and healthy controls. It was noted that serum KL-6 is a stable biomarker not affected by lung infection and smoking, though IPF patients with antinuclear antibody (ANA) showed higher KL-6 levels. KL-6, in conjunction with poor pulmonary function and higher radiological fibrosis scores, indicates the severity of the disease but not poor survival. CONCLUSIONS: It is identified that serum KL-6 is a useful noninvasive biomarker to help improve the certainty of IPF diagnosis from other interstitial lung disease and assist evaluation of disease severity and prognosis.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Pulmonares Intersticiales / Fibrosis Pulmonar Idiopática Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Clin Respir J Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades Pulmonares Intersticiales / Fibrosis Pulmonar Idiopática Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Clin Respir J Año: 2022 Tipo del documento: Article País de afiliación: China