• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

支气管扩张症患儿呼出气冷凝液中 MMP-9 的水平。

Exhaled breath condensate MMP-9 levels in children with bronchiectasis.

机构信息

Division of Pediatric Allergy and Immunology, Faculty of Medicine, University of Cukurova, Adana, Turkey.

出版信息

Pediatr Pulmonol. 2009 Oct;44(10):1010-6. doi: 10.1002/ppul.21096.

DOI:10.1002/ppul.21096
PMID:19725099
Abstract

Bronchiectasis (BE) is still an important cause of chronic supurative respiratory diseases in developing countries. Neutrophil-derived proteases such as neutrophil elastase and matrix metalloproteases (MMPs) are implicated in causing airway damage in chronic pulmonary disease. In this study, we aimed to evaluate the MMP-9 and its natural tissue inhibitors of metalloproteinases (TIMP-1) levels utilizing the exhaled breath condensate (EBC) method and their relationship with radiological findings and pulmonary functions in children with BE.Thirty-eight children with BE and 12 healthy children were included: Group 1 (cystic fibrosis [CF] BE), Group 2 (non-CF BE), Group 3 (control group). High-resolution computerized tomography (HRCT) scores were calculated according to the anatomic extent of BE. Pulmonary function tests were performed, and MMP-9 and TIMP-1 levels in EBC were analyzed by ELISA.Exhaled breath condensate MMP-9 level was 48.9 +/- 26.8 ng/ml for Group 1, and for Group 2, 42.8 +/- 18.1 ng/ml; and for Group 3, 30 +/- 3.7 ng/ml. Although no statistically significant difference was found between the Groups 1 and 2, a significant difference was detected between these groups and controls. No statistically significant difference was found in TIMP-1 levels regarding all groups. EBC MMP-9 levels were inversely correlated with pulmonary functions test, and positively with HRCT scores and annual number of pulmonary infections.In conclusion, this study showed that EBC of children with both CF BE and non-CF BE contained higher levels of MMP-9 in comparison to controls. We suggest that EBC MMP-9 level may be a useful marker of airway injury in patients with BE however prospective studies are needed.

摘要

支气管扩张症(BE)仍然是发展中国家慢性化脓性呼吸道疾病的重要原因。中性粒细胞衍生的蛋白酶,如中性粒细胞弹性蛋白酶和基质金属蛋白酶(MMPs),与慢性肺部疾病中的气道损伤有关。在这项研究中,我们旨在利用呼出气冷凝液(EBC)方法评估 MMP-9 及其天然金属蛋白酶抑制剂(TIMP-1)水平,并评估其与 BE 患儿的放射学发现和肺功能的关系。

纳入 38 例 BE 患儿和 12 例健康儿童:第 1 组(囊性纤维化[CF] BE),第 2 组(非 CF BE),第 3 组(对照组)。根据 BE 的解剖范围计算高分辨率计算机断层扫描(HRCT)评分。进行肺功能检查,并通过 ELISA 分析 EBC 中的 MMP-9 和 TIMP-1 水平。

第 1 组 EBC MMP-9 水平为 48.9±26.8ng/ml,第 2 组为 42.8±18.1ng/ml,第 3 组为 30±3.7ng/ml。尽管第 1 组和第 2 组之间无统计学差异,但与对照组相比,差异显著。三组间 TIMP-1 水平无统计学差异。EBC MMP-9 水平与肺功能测试呈负相关,与 HRCT 评分和每年肺部感染次数呈正相关。

综上所述,本研究表明 CF BE 和非 CF BE 患儿的 EBC 中 MMP-9 水平高于对照组。我们认为 EBC MMP-9 水平可能是 BE 患者气道损伤的有用标志物,但需要进一步的前瞻性研究。

相似文献

1
Exhaled breath condensate MMP-9 levels in children with bronchiectasis.支气管扩张症患儿呼出气冷凝液中 MMP-9 的水平。
Pediatr Pulmonol. 2009 Oct;44(10):1010-6. doi: 10.1002/ppul.21096.
2
Exhaled breath condensate MMP-9 level and its relationship wıth asthma severity and interleukin-4/10 levels in children.儿童呼出气冷凝物中 MMP-9 水平及其与哮喘严重程度和白细胞介素 4/10 水平的关系。
Ann Allergy Asthma Immunol. 2012 May;108(5):300-4. doi: 10.1016/j.anai.2012.02.019. Epub 2012 Mar 27.
3
Induced sputum matrix metalloproteinase-9 correlates with lung function and airway inflammation in children with cystic fibrosis.诱导痰基质金属蛋白酶-9与囊性纤维化患儿的肺功能及气道炎症相关。
Pediatr Pulmonol. 2005 Mar;39(3):224-32. doi: 10.1002/ppul.20165.
4
Enhanced exhalation of matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in patients with COPD exacerbation: a prospective study.COPD 加重期患者基质金属蛋白酶-9 和组织金属蛋白酶抑制剂-1 的呼出增加:一项前瞻性研究。
Respiration. 2012;84(3):231-41. doi: 10.1159/000339417. Epub 2012 Jul 24.
5
Exhaled breath condensate pH and exhaled nitric oxide in allergic asthma and in cystic fibrosis.过敏性哮喘和囊性纤维化患者的呼出气冷凝液pH值与呼出气一氧化氮水平
Thorax. 2005 Jan;60(1):22-6. doi: 10.1136/thx.2003.017327.
6
Longitudinal monitoring of pediatric cystic fibrosis lung disease using nitrite in exhaled breath condensate.利用呼出气体冷凝物中的亚硝酸盐对儿童囊性纤维化肺病进行纵向监测。
Pediatr Pulmonol. 2007 Dec;42(12):1198-206. doi: 10.1002/ppul.20719.
7
Exhaled breath condensate pH and ammonia in cystic fibrosis and response to treatment of acute pulmonary exacerbations.囊性纤维化患者呼出气冷凝液的pH值和氨含量以及对急性肺部加重期治疗的反应
Pediatr Pulmonol. 2009 Sep;44(9):866-72. doi: 10.1002/ppul.21078.
8
Inflammatory markers in exhaled breath condensate from patients with asthma.哮喘患者呼出气冷凝物中的炎症标志物。
Respirology. 2008 Sep;13(5):654-63. doi: 10.1111/j.1440-1843.2008.01315.x. Epub 2008 May 29.
9
Biomarkers in exhaled breath condensate indicate presence and severity of cystic fibrosis in children.呼出气体冷凝物中的生物标志物可表明儿童囊性纤维化的存在及严重程度。
Pediatr Allergy Immunol. 2008 Nov;19(7):652-9. doi: 10.1111/j.1399-3038.2007.00693.x. Epub 2008 Feb 27.
10
Biomarkers of neutrophilic inflammation in exhaled air of cystic fibrosis children with bacterial airway infections.患有细菌性气道感染的囊性纤维化儿童呼出气体中嗜中性粒细胞炎症的生物标志物。
Pediatr Pulmonol. 2005 Dec;40(6):494-9. doi: 10.1002/ppul.20336.

引用本文的文献

1
A cross-sectional study on the comparison of serum SIRT-1 and MMP-9 levels of patients with bronchiectasis and healthy controls.一项关于支气管扩张症患者与健康对照者血清SIRT-1和MMP-9水平比较的横断面研究。
Pak J Med Sci. 2025 Apr;41(4):1052-1057. doi: 10.12669/pjms.41.4.10877.
2
The role of volatile organic compounds for assessing characteristics and severity of non-cystic fibrosis bronchiectasis: an observational study.挥发性有机化合物在评估非囊性纤维化支气管扩张症特征和严重程度中的作用:一项观察性研究。
Front Med (Lausanne). 2024 Apr 3;11:1345165. doi: 10.3389/fmed.2024.1345165. eCollection 2024.
3
A pediatric disease to keep in mind: diagnostic tools and management of bronchiectasis in pediatric age.
需要牢记的儿科疾病:儿科支气管扩张症的诊断工具和管理。
Ital J Pediatr. 2017 Dec 29;43(1):117. doi: 10.1186/s13052-017-0434-0.
4
Neutrophil Fates in Bronchiectasis and Alpha-1 Antitrypsin Deficiency.支气管扩张症和α-1抗胰蛋白酶缺乏症中的中性粒细胞命运
Ann Am Thorac Soc. 2016 Apr;13 Suppl 2(Suppl 2):S123-9. doi: 10.1513/AnnalsATS.201512-805KV.
5
Elevated Expression of Matrix Metalloproteinase-9 not Matrix Metalloproteinase-2 Contributes to Progression of Extracranial Arteriovenous Malformation.基质金属蛋白酶-9而非基质金属蛋白酶-2的表达升高促进颅外动静脉畸形的进展。
Sci Rep. 2016 Apr 14;6:24378. doi: 10.1038/srep24378.
6
Acute exacerbations of COPD are associated with significant activation of matrix metalloproteinase 9 irrespectively of airway obstruction, emphysema and infection.慢性阻塞性肺疾病急性加重与基质金属蛋白酶9的显著激活相关,而与气道阻塞、肺气肿和感染无关。
Respir Res. 2015 Jun 28;16(1):78. doi: 10.1186/s12931-015-0240-4.
7
Gender susceptibility to mycobacterial infections in patients with non-CF bronchiectasis.非囊性纤维化支气管扩张症患者中性别对分枝杆菌感染的易感性
Int J Mycobacteriol. 2015 Jun;4(2):92-6. doi: 10.1016/j.ijmyco.2015.05.002.
8
The etiologies of non-CF bronchiectasis in childhood: a systematic review of 989 subjects.儿童非囊性纤维化支气管扩张症的病因:对989例受试者的系统评价
BMC Pediatr. 2014 Dec 10;14:4. doi: 10.1186/s12887-014-0299-y.
9
Low-dose clarithromycin therapy modulates Th17 response in non-cystic fibrosis bronchiectasis patients.小剂量克拉霉素治疗可调节非囊性纤维化支气管扩张症患者的 Th17 反应。
Lung. 2014 Dec;192(6):849-55. doi: 10.1007/s00408-014-9619-0. Epub 2014 Jul 14.
10
Airway inflammatory markers in individuals with cystic fibrosis and non-cystic fibrosis bronchiectasis.囊性纤维化和非囊性纤维化支气管扩张症患者的气道炎症标志物。
J Inflamm Res. 2013;6:1-11. doi: 10.2147/JIR.S40081. Epub 2013 Jan 23.