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1.
J Cardiopulm Rehabil Prev ; 43(2): 122-128, 2023 03 01.
Article in English | MEDLINE | ID: mdl-36223406

ABSTRACT

PURPOSE: The objective of this investigation was to determine whether chronic obstructive pulmonary disease (COPD) patients with high blood eosinophil (EOS) counts had better improvement in 6-min walk test (6MWT) after pulmonary rehabilitation (PR). METHODS: Fifty COPD patients were randomly assigned to either the rehabilitation group (RG) or the control group (CG). Patients in the RG (8 wk PR + routine medication) and the CG (routine medication) were followed for 32 wk. According to the blood EOS level, the RG was divided into an EOS ≥ 200 cells/µL group and EOS < 200 cells/µL group. The 6MWT distance, Borg Scale, and COPD Assessment Test (CAT) were evaluated before intervention and 8 wk and 32 wk later. RESULTS: After the 8-wk intervention, 37 patients (19 RG/18 CG) completed the study. At 8-wk and 32-wk follow-up from baseline, a statistically significant difference was found between these two groups in the 6MWT, Borg Scale, and CAT. Compared with baseline, the 6MWT in the RG increased 49.1 ± 40.2 m (95% CI, 29.7-68.5, P < .001) at 8 wk and 60.8 ± 42.1 m (95% CI, 40.5-81.6, P < .001) at 32 wk. In addition, the improvement of 6MWT in the EOS ≥ 200 cells/µL RG group was higher than that in the EOS < 200 cells/µL group (40.1 ± 17.6 m, 95% CI, 36.8-43.4; P = .036) at 32-wk follow-up from baseline. CONCLUSION: An 8-wk PR can improve the exercise capacity of COPD patients, and the benefits persistent for 24 wk. The improvement in the 6MWT was more significant in COPD patients with a high blood EOS count.


Subject(s)
Eosinophils , Pulmonary Disease, Chronic Obstructive , Humans , Walk Test
2.
Zhonghua Gan Zang Bing Za Zhi ; 14(8): 561-4, 2006 Aug.
Article in Chinese | MEDLINE | ID: mdl-16938163

ABSTRACT

OBJECTIVE: To screen and identify proteins that interact with hepatitis C virus NS3 by means of T7-phage display system. METHODS: Hepatitis C virus NS3 was expressed by prokaryotic expression and used as a selected molecule to biopan the T7 select human liver cDNA library; the selected positive clones were identified using DNA sequencing and analyzed with BLAST program in GenBank. RESULTS: After BLAST analysis in all the positive clones, the proteins which interacted with the hepatitis C virus NS3 were found to be serpin peptidase inhibitor, clade A, member 1 (SERPINA1) and cyclophilin-LC. CONCLUSION: T7-phage display system is a convenient, rapid and effective method for screening interacting proteins. The proteins thus selected will provide an important means for studying the pathogenesis and carcinogenesis of HCV.


Subject(s)
Hepacivirus/metabolism , Protein Interaction Mapping/methods , Viral Nonstructural Proteins/genetics , Cell Line , Gene Library , Humans , Peptide Library , Viral Fusion Proteins/genetics , Viral Fusion Proteins/isolation & purification , Viral Fusion Proteins/metabolism , Viral Nonstructural Proteins/metabolism
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