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排序方式: 共有461条查询结果,搜索用时 15 毫秒
51.
《COPD》2013,10(1):17-25
We have previously reported diminished immunohistochemical staining of decorin in lung tissue from patients with severe emphysema. The aim of this study is to investigate whether this diminished staining is due to a quantitative abnormal production of decorin by pulmonary fibroblasts in vitro. Therefore, we measured decorin (Western blot), collagen type I (ELISA), and fibronectin (ELISA) production by fibroblasts obtained from lung tissue of patients with severe and mild emphysema at basal culture conditions and after modulation with transforming growth factor-β1, basic fibroblast growth factor, and interferon-γ. Decorin production at basal culture conditions was significantly higher in fibroblast cultures from patients with severe emphysema compared to fibroblasts from mild emphysema. After stimulation with transforming growth factor-β1 and basic fibroblast growth factor, decorin production was significantly more reduced in fibroblast cultures from patients with severe emphysema whereas collagen type I and fibronectin production were not affected. We conclude that decorin production by lung fibroblasts of patients with severe emphysema is dysregulated after modulation with cytokines known to be important in smoking associated inflammation. This dysregulation of decorin production may contribute to the impaired lung tissue repair, present in patients with emphysema, since these alterations in the extracellular matrix may cause diminished cytokine binding and neutralization. 相似文献
52.
《COPD》2013,10(5):329-333
Desmosine and isodesmosine are products of elastin breakdown which are candidate biomarkers to measure lung destruction in COPD. Data exist on the burden of desmosines in urine and plasma in COPD but long-term changes have never been investigated. We determined the changes of desmosine levels over 14 months in urine and plasma of patients with type ZZ alpha-1-antitryspsin deficiency-related COPD. Urines and plasma for determination of desmosines were collected from 11 ex-smokers with moderate/severe emphysema at monthly intervals for 14 months. Spirometry and gas transfer were assessed at baseline and 6-month intervals. At baseline and month 14, eleven healthy partners of patients volunteered to give a blood sample for detection of desmosines. Desmosines were determined by capillary electrophoresis combined with laser-induced fluorescence. Urine and plasma desmosines were significantly increased after 14 months in patients (p = 0.027 and p = 0.0005, respectively). Plasma desmosines of healthy partners at baseline were 4-fold lower than from patients and not significantly different from values at month 14. Only a significant decline in lung gas transfer occurred in patients (p = 0.015). The variability of desmosines was higher in urine than in plasma (coefficient of variation 0.17 and 0.087, respectively). As longitudinal desmosine changes likely reflect the elevated elastic fiber turnover associated with the progression of lung damage and destruction in COPD, they appear to be a suitable marker for application in long-term studies. Plasma desmosines were more stable long-term biomarkers than desmosines in urine. 相似文献
53.
《COPD》2013,10(3):182-188
Background: Sleep quality is poor in severe emphysema. We hypothesized that in addition to nocturnal oxygen desaturation, the severity of airflow obstruction and degree of thoracic hyperinflation are responsible. Methods: Twenty-five patients (14 males, 64 ± 6 [ ± SD] yrs, BMI 24.7 ± 4.2 kg/m2) with severe emphysema (FEV1 = 28 ± 8% predicted, TLC = 125 ± 14% predicted) were studied. Measurements included spirometry, lung volumes, arterial blood gas, length of the diaphragm's zone of apposition (LZAP) and a polysomnogram. Results: Total sleep time (TST) was 227 ± 93 minutes with a sleep efficiency (SE) of 56 ± 21%. The mean SaO2, lowest SaO2, and% TST with a SaO2 < 90% were 90 ± 5%, 83 ± 8% and 29 ± 40%, respectively. TST correlated with FEV1% (r = 0.5, p = 0.02), FVC% (r = 0.4, p = 0.03) and LZAP (r = 0.5, p = 0.01). SE correlated with FEV1% (r = 0.5, p = 0.02) and LZAP (r = 0.5, p = 0.01), but not with FVC% (r = 0.4, p = 0.07). Additionally, TST and SE correlated negatively with residual volume% (r = -0.4, p = 0.046, and r = -0.4, p = 0.03, respectively). There was no correlation between TST and SE and measures of nocturnal oxygenation. Multiple linear regression was used to predict TST, with 50% (r2 = 0.49) explained by a combination of LZAP (27%), mean SaO2 (23%), and the lowest SaO2 (< 1%). To predict SE, 44% (r2 = 0.43) was explained by a combination of LZAP (29%), mean SaO2 (14%), and the lowest SaO2 (1%). Conclusion: Although parameters of respiratory function and mechanics correlate with sleep quality, both nocturnal oxygenation and measurements of respiratory function/mechanics predict sleep quality in severe emphysema. 相似文献
54.
内科微创肺减容术的研究进展 总被引:1,自引:0,他引:1
传统的外科肺减容术治疗慢性阻塞性肺疾病(COPD)有严格的适应证,并且副作用大、并发症多。于是人们研究出多种基于同样原理但是采用内科微创技术的减容方法。目前常用的内科微创肺减容术有使用单向活瓣、生物蛋白胶等封堵支气管使靶肺萎陷、不张,或采用支气管内药物灌注肺泡加封堵使靶肺组织纤维化等。此外,还有人提出人工旁路增加呼出气量的方法。尽管目前还缺少大规模的随机对照临床试验结果,但是内科微创肺减容术已展现了其巨大的临床应用前景,也将为治疗COPD提供更多的选择。 相似文献
55.
R. Lange G. Worth U. Smidt W. Stahlmann 《International archives of occupational and environmental health》1980,45(3):251-259
Summary In fifteen hundred sixty-one radiographs from 318 coal workers with different grades of pneumoconiosis, the prevalence of perinodular, perinodal, and generalized emphysema has been examined. Furthermore, the prevalence of enlarged hili was determined. These data have been correlated with age and the type, number and density of small pneumoconiotic opacities and with the size and localization of large pneumoconiotic opacities.Some form of emphysema was found in 86.7% of all radiographs, most frequently in the form of generalized emphysema (63.6%). The prevalence increases with severity of pneumoconiosis. The same holds for enlarged hili.With support of the European Communities, Luxembourg 相似文献
56.
57.
报道1例以黄疸为表现的α1-抗胰蛋白酶缺乏症病例,该例患者初始起病以黄疸为表现,病程10年,通过肝活检组织病理确诊。结合文献对α1-抗胰蛋白酶缺乏症的流行病学现状、病因机制、临床表现及治疗预后加以复习,藉此对临床遗传性肝病的诊治提供参考。 相似文献
58.
Xiangdong Wang Yaoli Wang Xia Zhao Roland Andersson Zhenju Song Dong Yang Chunxue Bai 《Pulmonary pharmacology & therapeutics》2009,22(4):318-325
Multiple factors contribute to the pathogenesis and prognosis of chronic obstructive pulmonary disease (COPD), still requiring new therapeutic strategies and medications for the disease. The aim of the present study is to investigate the model of lipopolysaccharide (LPS)-induced chronic lung injury and hyperinflation and test therapeutic effects of peroxisome proliferator-activated receptor (PPAR)-γ agonist. Wister rats were challenged with intra-tracheal instillation of LPS at concentrations of 0.006, 0.060, 0.600, and 6.000 mg/ml per kg, twice a week, for 1, 2, 4 and 6 weeks. PPAR activator, 15-deoxy-Δ12,14-prostaglandin J2 (15D-PGJ2), or vehicle (PBS) was administered orally and daily at the dose of 1 and 10 mg/ml per kg in animals challenged with LPS or PBS at the dose of 0.060 mg/ml per kg body weight twice a week for 4 weeks. We found that intra-tracheal exposure of LPS resulted in a dose-dependent pattern of chronic lung hyperinflation and hypertrophy, increased alveolar enlargement, reduced vascular endothelial growth factor (VEGF) and elevated tissue inhibitor of metalloproteinases (TIMP)-1 levels in bronchoalveolar lavage (BAL) fluid, and early changes of leukocyte influx and interferon (IFN)-γ levels in bronchoalveolar lavage (BAL) fluid. PPAR-γ agonist ameliorated these changes related with the dose used. LPS-induced lung disease model shows some similarities with human disease, and PPAR-γ agonist may be an alternative for COPD therapy. 相似文献
59.
肺减容术是治疗晚期肺气肿的选择之一,外科肺减容术由于其并发症、病死率及治疗费用等限制其发展.但促进了经支气管镜肺减容术的发展.目前包括经支气管镜旁路通气法肺减容术,经支气管镜生物学肺减容术,经支气管镜单向活瓣放置肺减容术,其微创、简便、痛苦及其并发症少等特点展现了其巨大的临床应用前景. 相似文献
60.
R. Graham Barr Bartolome R. Celli David M. Mannino Thomas Petty Stephen I. Rennard Frank C. Sciurba James K. Stoller Byron M. Thomashow Gerard M. Turino 《The American journal of medicine》2009,122(4):348-355