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本文引用的文献

1
Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis.在成人和儿童囊性纤维化患者中,肺部恶化与随后的 FEV1 下降有关。
Pediatr Pulmonol. 2011 Apr;46(4):393-400. doi: 10.1002/ppul.21374. Epub 2010 Oct 21.
2
Exhaled nitric oxide in pulmonary diseases: a comprehensive review.呼气一氧化氮在肺部疾病中的应用:全面综述。
Chest. 2010 Sep;138(3):682-92. doi: 10.1378/chest.09-2090.
3
Revealing the dynamics of polymicrobial infections: implications for antibiotic therapy.揭示多微生物感染的动态:对抗生素治疗的影响。
Trends Microbiol. 2010 Aug;18(8):357-64. doi: 10.1016/j.tim.2010.04.005. Epub 2010 Jun 1.
4
Structural lung changes, lung function, and non-invasive inflammatory markers in cystic fibrosis.囊性纤维化中的结构性肺改变、肺功能和非侵入性炎症标志物。
Pediatr Allergy Immunol. 2010 May;21(3):493-500. doi: 10.1111/j.1399-3038.2009.00872.x.
5
Rhinovirus C and respiratory exacerbations in children with cystic fibrosis.鼻病毒 C 与囊性纤维化患儿的呼吸道恶化。
Emerg Infect Dis. 2010 Jun;16(6):996-9. doi: 10.3201/eid1606.100063.
6
Comparison of the Eragen Multi-Code Respiratory Virus Panel with conventional viral testing and real-time multiplex PCR assays for detection of respiratory viruses.比较 Eragen Multi-Code 呼吸道病毒检测试剂盒与常规病毒检测和实时多重 PCR 检测试剂盒在呼吸道病毒检测中的应用。
J Clin Microbiol. 2010 Jul;48(7):2387-95. doi: 10.1128/JCM.00220-10. Epub 2010 May 19.
7
Sputum Candida albicans presages FEV₁ decline and hospital-treated exacerbations in cystic fibrosis.白色念珠菌痰预示着囊性纤维化患者的 FEV₁ 下降和需要住院治疗的加重。
Chest. 2010 Nov;138(5):1186-95. doi: 10.1378/chest.09-2996. Epub 2010 May 14.
8
Failure to recover to baseline pulmonary function after cystic fibrosis pulmonary exacerbation.囊性纤维化肺部恶化后未能恢复到基线肺功能。
Am J Respir Crit Care Med. 2010 Sep 1;182(5):627-32. doi: 10.1164/rccm.200909-1421OC. Epub 2010 May 12.
9
Isolation of Exophiala dermatitidis from pigmented sputum in a cystic fibrosis patient.从囊性纤维化患者的色素性痰中分离出皮炎外瓶霉。
Pediatr Pulmonol. 2010 May;45(5):508-10. doi: 10.1002/ppul.21187.
10
The utility of biomarkers in sorting out the complex patient.生物标志物在理清复杂患者中的作用。
Am J Med. 2010 May;123(5):393-9. doi: 10.1016/j.amjmed.2009.07.034.

利用细菌生物标志物识别囊性纤维化肺部恶化发作的早期指标。

Using bacterial biomarkers to identify early indicators of cystic fibrosis pulmonary exacerbation onset.

机构信息

Molecular Microbiology Research Laboratory, Pharmaceutical Science Division, 150 Stamford Street, Franklin-Wilkins Building, King's College London, London, SE1 9NH, UK.

出版信息

Expert Rev Mol Diagn. 2011 Mar;11(2):197-206. doi: 10.1586/erm.10.117.

DOI:10.1586/erm.10.117
PMID:21405970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3148893/
Abstract

Acute periods of pulmonary exacerbation are the single most important cause of morbidity in cystic fibrosis patients, and may be associated with a loss of lung function. Intervening prior to the onset of a substantially increased inflammatory response may limit the associated damage to the airways. While a number of biomarker assays based on inflammatory markers have been developed, providing useful and important measures of disease during these periods, such factors are typically only elevated once the process of exacerbation has been initiated. Identifying biomarkers that can predict the onset of pulmonary exacerbation at an early stage would provide an opportunity to intervene before the establishment of a substantial immune response, with major implications for the advancement of cystic fibrosis care. The precise triggers of pulmonary exacerbation remain to be determined; however, the majority of models relate to the activity of microbes present in the patient's lower airways of cystic fibrosis. Advances in diagnostic microbiology now allow for the examination of these complex systems at a level likely to identify factors on which biomarker assays can be based. In this article, we discuss key considerations in the design and testing of assays that could predict pulmonary exacerbations.

摘要

急性肺部恶化期是囊性纤维化患者发病的最主要原因,可能导致肺功能丧失。在炎症反应显著增加之前进行干预,可能有助于限制气道的相关损伤。虽然已经开发出许多基于炎症标志物的生物标志物检测方法,为这些时期的疾病提供了有用和重要的衡量指标,但这些因素通常仅在恶化过程开始后才会升高。确定能够在早期预测肺部恶化发作的生物标志物,将为在建立实质性免疫反应之前进行干预提供机会,这对囊性纤维化护理的发展具有重大意义。肺部恶化的确切触发因素仍有待确定;然而,大多数模型都与囊性纤维化患者下呼吸道中存在的微生物的活性有关。诊断微生物学的进步现在可以在可能确定生物标志物检测方法可以依据的因素的水平上检查这些复杂的系统。在本文中,我们讨论了设计和测试能够预测肺部恶化的检测方法的关键考虑因素。