• 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

[特发性肺纤维化和结节病患者血清及支气管肺泡灌洗液中基质金属蛋白酶-1和基质金属蛋白酶-7的变化]

[Change of matrix metalloproteinase-1 and matrix metalloproteinase-7 in serum and bronchoalveolar lavage fluid of patients with idiopathic pulmonary fibrosis and sarcoidosis].

作者信息

Zhou Le-fei, Jiang Li, Li Zhen-hua, Kang Jian

机构信息

Institute of Respiratory Disease, First Affiliated Hospital, China Medical University, Shenyang 110001, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2010 Jun;33(6):441-4.

PMID:20979817
Abstract

OBJECTIVE

To detect the levels of matrix metalloprotease (MMP)-1 and MMP-7 in the serum and the bronchoalveolar lavage fluid (BALF) of patients with idiopathic pulmonary fibrosis (IPF) and sarcoidosis (Stage II), and therefore to investigate the significance of these changes in the pathogenesis of IPF.

METHODS

Forty-four clinically confirmed cases of IPF were recruited, with the patients' age ranging from 46 to 70 years (58 ± 9 years). Twenty patients with sarcoidosis, aged 35 to 65 (50 ± 12) years, were also studied. Enzyme-linked immunoabsorbent assay was used to detect the levels of MMP-1 and MMP-7 in the serum and the BALF samples.

RESULTS

In the serum of patients with IPF, the level of MMP-1 [3.78 (0.14 - 13.44) µg/L] was lower than that in patients with sarcoidosis [7.79 (4.67 - 10.68) µg/L (z = -3.53, P < 0.01)], but the level of MMP-7 [7.83 (3.57 - 14.37) µg/L] was higher than that in patients with sarcoidosis [4.04 (0.06 - 9.94) µg/L (z = -3.84, P < 0.01)]. In the BALF of patients with IPF, the level of MMP-1 [1.09 (0.04 - 5.14) µg/L] was lower than that in patients with sarcoidosis [2.08 (0.05 - 4.16) µg/L (z = -1.53, P > 0.05)], but the level of MMP-7 [3.75 (1.10 - 9.87)µg/L] was higher than that in patients with sarcoidosis [1.16 (0.02 - 4.47) µg/L (z = -5.33, P < 0.01)]. The serum level of MMP-7 in patients with IPF was negatively correlated with the diffusing capacity of carbon monoxide(r = -0.56, P < 0.01) and the percentage of neutrophils (r = -0.47, P < 0.01). The level of MMP-7 in the BALF showed a negative correlation with diffusing capacity of carbon monoxide (r = -0.31, P < 0.05).

CONCLUSIONS

The results suggest that MMP-1 may be increased in the inflammatory phase as compared to the matrix remodeling phase of lung fibrosis, while MMP-7 may be increased in the matrix remodeling phase rather than in the inflammatory phase. MMP-7 may act as an important indicator for the severity of IPF.

摘要

目的

检测特发性肺纤维化(IPF)和结节病(Ⅱ期)患者血清及支气管肺泡灌洗液(BALF)中基质金属蛋白酶(MMP)-1和MMP-7的水平,从而探讨这些变化在IPF发病机制中的意义。

方法

招募44例临床确诊的IPF患者,患者年龄46至70岁(58±9岁)。还研究了20例年龄在35至65岁(50±12岁)的结节病患者。采用酶联免疫吸附测定法检测血清和BALF样本中MMP-1和MMP-7的水平。

结果

IPF患者血清中MMP-1水平[3.78(0.14 - 13.44)μg/L]低于结节病患者[7.79(4.67 - 10.68)μg/L(z = -3.53,P < 0.01)],但MMP-7水平[7.83(3.57 - 14.37)μg/L]高于结节病患者[4.04(0.06 - 9.94)μg/L(z = -3.84,P < 0.01)]。IPF患者BALF中MMP-1水平[1.09(0.04 - 5.14)μg/L]低于结节病患者[2.08(0.05 - 4.16)μg/L(z = -1.53,P > 0.05)],但MMP-7水平[3.75(1.10 - 9.87)μg/L]高于结节病患者[1.16(0.02 - 4.47)μg/L(z = -5.33,P < 0.01)]。IPF患者血清MMP-7水平与一氧化碳弥散量呈负相关(r = -0.56,P < 0.01),与中性粒细胞百分比呈负相关(r = -0.47,P < 0.01)。BALF中MMP-7水平与一氧化碳弥散量呈负相关(r = -0.31,P < 0.05)。

结论

结果表明,与肺纤维化的基质重塑期相比,MMP-1可能在炎症期升高,而MMP-7可能在基质重塑期而非炎症期升高。MMP-7可能是IPF严重程度的重要指标。

相似文献

1
[Change of matrix metalloproteinase-1 and matrix metalloproteinase-7 in serum and bronchoalveolar lavage fluid of patients with idiopathic pulmonary fibrosis and sarcoidosis].[特发性肺纤维化和结节病患者血清及支气管肺泡灌洗液中基质金属蛋白酶-1和基质金属蛋白酶-7的变化]
Zhonghua Jie He He Hu Xi Za Zhi. 2010 Jun;33(6):441-4.
2
[Changes of matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in the bronchoalveolar lavage fluid and the serum of patients with idiopathic pulmonary fibrosis].[特发性肺纤维化患者支气管肺泡灌洗液及血清中基质金属蛋白酶-9和金属蛋白酶组织抑制剂-1的变化]
Zhonghua Jie He He Hu Xi Za Zhi. 2006 Jun;29(6):399-402.
3
[Changes of the activities of ET-1 in the serum and BALF of ILD patients and their clinical significance].[特发性间质性肺炎患者血清及支气管肺泡灌洗液中内皮素-1活性变化及其临床意义]
Zhonghua Jie He He Hu Xi Za Zhi. 1999 Jul;22(7):411-3.
4
Elevated matrilysin levels in bronchoalveolar lavage fluid do not distinguish idiopathic pulmonary fibrosis from other interstitial lung diseases.支气管肺泡灌洗液体中基质溶解素水平升高并不能区分特发性肺纤维化与其他间质性肺疾病。
APMIS. 2007 Aug;115(8):969-75. doi: 10.1111/j.1600-0463.2007.apm_697.x.
5
Can circulating interleukin-18 differentiate between sarcoidosis and idiopathic pulmonary fibrosis?循环白细胞介素-18 能否区分结节病和特发性肺纤维化?
Scand J Clin Lab Invest. 2011 Nov;71(7):593-7. doi: 10.3109/00365513.2011.597871. Epub 2011 Aug 11.
6
[Level of NCF and TNF-alpha in the BALF of ILD patients and their clinical significance].[ILD患者BALF中NCF和TNF-α水平及其临床意义]
Zhonghua Jie He He Hu Xi Za Zhi. 1998 May;21(5):297-9.
7
Matrix metalloproteinase-10: a novel biomarker for idiopathic pulmonary fibrosis.基质金属蛋白酶-10:特发性肺纤维化的一种新型生物标志物。
Respir Res. 2015 Sep 29;16:120. doi: 10.1186/s12931-015-0280-9.
8
[Detection of TNF-alpha and NCF in the serum and BALF of patients with sarcoidosis and evaluate their clinical significance].[结节病患者血清及支气管肺泡灌洗液中TNF-α和NCF的检测及其临床意义评估]
Zhonghua Jie He He Hu Xi Za Zhi. 1999 Jan;22(1):37-9.
9
[Evaluation of interleukin-13 in the serum and bronchoalveolar lavage fluid of patients with idiopathic pulmonary fibrosis].[特发性肺纤维化患者血清和支气管肺泡灌洗液中白细胞介素-13的评估]
Zhonghua Jie He He Hu Xi Za Zhi. 2003 Nov;26(11):686-8.
10
Serum metalloproteinases 1 and 7 in the diagnosis of idiopathic pulmonary fibrosis and other interstitial pneumonias.血清金属蛋白酶1和7在特发性肺纤维化及其他间质性肺炎诊断中的应用
Respir Med. 2015 Aug;109(8):1063-8. doi: 10.1016/j.rmed.2015.06.003. Epub 2015 Jun 12.

引用本文的文献

1
Emerging delivery approaches for targeted pulmonary fibrosis treatment.靶向肺纤维化治疗的新兴给药途径。
Adv Drug Deliv Rev. 2024 Jan;204:115147. doi: 10.1016/j.addr.2023.115147. Epub 2023 Dec 6.
2
Comparative Analysis of Gene Expression in Fibroblastic Foci in Patients with Idiopathic Pulmonary Fibrosis and Pulmonary Sarcoidosis.特发性肺纤维化和肺结节病患者成纤维灶中基因表达的比较分析。
Cells. 2022 Feb 14;11(4):664. doi: 10.3390/cells11040664.
3
Idiopathic pulmonary fibrosis: Epithelial-mesenchymal interactions and emerging therapeutic targets.
特发性肺纤维化:上皮-间充质相互作用和新的治疗靶点。
Matrix Biol. 2018 Oct;71-72:112-127. doi: 10.1016/j.matbio.2018.03.021. Epub 2018 Apr 3.
4
The elevation of serum napsin A in idiopathic pulmonary fibrosis, compared with KL-6, surfactant protein-A and surfactant protein-D.血清 Napsin A 在特发性肺纤维化中的水平升高,与 KL-6、表面活性蛋白-A 和表面活性蛋白-D 相比。
BMC Pulm Med. 2012 Sep 11;12:55. doi: 10.1186/1471-2466-12-55.