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特发性肺纤维化患者气管直径与呼吸功能及纤维化严重程度的相关性

Association of tracheal diameter with respiratory function and fibrosis severity in idiopathic pulmonary fibrosis patients.

作者信息

Fazlıoğlu Nevin, Sasani Hadi, Fazlıoğlu Mithat, Çiftçi Ezgi Pınar, Mutlu Levent Cem

机构信息

Department of Pulmonology, Faculty of Medicine, Tekirdag Namik Kemal University, Tekirdag, 59030, Turkey.

Department of Radiology, Faculty of Medicine, Tekirdag Namik Kemal University, Tekirdag, Turkey.

出版信息

BMC Pulm Med. 2025 Apr 5;25(1):157. doi: 10.1186/s12890-025-03624-x.

DOI:10.1186/s12890-025-03624-x
PMID:40188355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11972493/
Abstract

BACKGROUND

In this research project, we examined the relationship between tracheal size and respiratory function in individuals with Idiopathic Pulmonary Fibrosis (IPF). IPF is a long-term condition that affects the functioning of the lungs.

METHODS

This retrospective study included 86 patients diagnosed with IPF. Tracheal and bronchial diameters were measured using high-resolution computed tomography (HRCT) and pulmonary function tests (PFTs); Force vital capacity (FVC), diffusion capacity for carbon monoxide (DLCO) and the gender, age, physiology (GAP) index was calculated. Patients were grouped according to demographic characteristics such as age, gender and smoking.

RESULTS

There was a significant positive correlation between the anteroposterior (AP) and transverse diameters of the trachea in the subcricoid region and the GAP index (r = 0.318, p = 0.003 and r = 0.312, p = 0.004, respectively). Similarly, subcricoid and carina areas were significantly correlated with both GAP index (r = 0.307, p = 0.006 and r = 0.334, p = 0.003, respectively) and FVC/DLCO ratio (r = 0.218, p = 0.049 and r = 0.245, p = 0.027, respectively). The main bronchial areas were also positively correlated with the GAP index, but no significant correlation was found between FVC and DLCO values and airway measurements. Each unit increase in GAP index was associated with a 1.69-fold increase in mortality risk (p = 0.0016, 95% confidence interval: 1.22-2.34).

CONCLUSION

Tracheal and main bronchial areas can be used as potential biomarkers in the assessment of disease severity and prognosis in IPF patients. In particular, the significant correlation of subcricoid and carina areas with both GAP index and FVC/DLCO ratio suggests that these measurements may be useful in the evaluation of disease progression.

摘要

背景

在本研究项目中,我们研究了特发性肺纤维化(IPF)患者气管大小与呼吸功能之间的关系。IPF是一种影响肺部功能的长期病症。

方法

这项回顾性研究纳入了86例确诊为IPF的患者。使用高分辨率计算机断层扫描(HRCT)和肺功能测试(PFT)测量气管和支气管直径;计算用力肺活量(FVC)、一氧化碳弥散量(DLCO)以及性别、年龄、生理学(GAP)指数。根据年龄、性别和吸烟等人口统计学特征对患者进行分组。

结果

环状软骨下区域气管的前后径和横径与GAP指数之间存在显著正相关(分别为r = 0.318,p = 0.003和r = 0.312,p = 0.004)。同样,环状软骨下区域和隆突区域与GAP指数(分别为r = 0.307,p = 0.006和r = 0.334,p = 0.003)以及FVC/DLCO比值(分别为r = 0.218,p = 0.049和r = 0.245,p = 0.027)均显著相关。主支气管区域也与GAP指数呈正相关,但未发现FVC和DLCO值与气道测量值之间存在显著相关性。GAP指数每增加一个单位,死亡风险增加1.69倍(p = 0.0016,95%置信区间:1.22 - 2.34)。

结论

气管和主支气管区域可作为评估IPF患者疾病严重程度和预后的潜在生物标志物。特别是,环状软骨下区域和隆突区域与GAP指数以及FVC/DLCO比值显著相关,表明这些测量值可能有助于评估疾病进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc20/11972493/0db94aca8c12/12890_2025_3624_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc20/11972493/0db94aca8c12/12890_2025_3624_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc20/11972493/0db94aca8c12/12890_2025_3624_Fig1_HTML.jpg

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本文引用的文献

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Respirology. 2024 Nov;29(11):962-968. doi: 10.1111/resp.14811. Epub 2024 Aug 15.
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Bronchial Asthma, Airway Remodeling and Lung Fibrosis as Successive Steps of One Process.支气管哮喘、气道重塑和肺纤维化作为一个过程的连续步骤。
Int J Mol Sci. 2023 Nov 7;24(22):16042. doi: 10.3390/ijms242216042.
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Multi-Step Extracellular Matrix Remodelling and Stiffening in the Development of Idiopathic Pulmonary Fibrosis.特发性肺纤维化发病过程中的多步骤细胞外基质重塑和僵硬。
Int J Mol Sci. 2023 Jan 15;24(2):1708. doi: 10.3390/ijms24021708.
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The Pathogenesis of Bronchiectasis.支气管扩张症的发病机制。
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Biomechanical Force and Cellular Stiffness in Lung Fibrosis.肺纤维化中的生物力学力和细胞硬度。
Am J Pathol. 2022 May;192(5):750-761. doi: 10.1016/j.ajpath.2022.02.001. Epub 2022 Feb 17.
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Circulating fibrocytes are not disease-specific prognosticators in idiopathic pulmonary fibrosis.循环成纤维细胞不是特发性肺纤维化的疾病特异性预后标志物。
Eur Respir J. 2021 Jul 22;58(1). doi: 10.1183/13993003.00172-2021. Print 2021 Jul.
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Real-World Study Analysing Progression and Survival of Patients with Idiopathic Pulmonary Fibrosis with Preserved Lung Function on Antifibrotic Treatment.真实世界研究分析接受抗纤维化治疗的肺功能保留的特发性肺纤维化患者的进展和生存情况。
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