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本文引用的文献

1
Five-year Progression of Emphysema and Air Trapping at CT in Smokers with and Those without Chronic Obstructive Pulmonary Disease: Results from the COPDGene Study.吸烟者中存在和不存在慢性阻塞性肺疾病(COPD)者的 CT 肺气肿和空气潴留的 5 年进展:来自 COPDGene 研究的结果。
Radiology. 2020 Apr;295(1):218-226. doi: 10.1148/radiol.2020191429. Epub 2020 Feb 4.
2
Relationship between diffusion capacity and small airway abnormality in COPDGene.COPDGene 中弥散能力与小气道异常的关系。
Respir Res. 2019 Dec 2;20(1):269. doi: 10.1186/s12931-019-1237-1.
3
Voxel-Wise Longitudinal Parametric Response Mapping Analysis of Chest Computed Tomography in Smokers.吸烟者胸部 CT 体素内纵向参数反应映射分析。
Acad Radiol. 2019 Feb;26(2):217-223. doi: 10.1016/j.acra.2018.05.024. Epub 2018 Jul 26.
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Clinical Significance of Symptoms in Smokers with Preserved Pulmonary Function.肺功能正常的吸烟者症状的临床意义
N Engl J Med. 2016 May 12;374(19):1811-21. doi: 10.1056/NEJMoa1505971.
5
Association between Functional Small Airway Disease and FEV1 Decline in Chronic Obstructive Pulmonary Disease.慢性阻塞性肺疾病中功能性小气道疾病与第一秒用力呼气容积下降之间的关联
Am J Respir Crit Care Med. 2016 Jul 15;194(2):178-84. doi: 10.1164/rccm.201511-2219OC.
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The Impact of Sources of Variability on Parametric Response Mapping of Lung CT Scans.变异性来源对肺部CT扫描参数响应映射的影响。
Tomography. 2015 Sep;1(1):69-77. doi: 10.18383/j.tom.2015.00148.
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Sex-specific features of emphysema among current and former smokers with COPD.慢性阻塞性肺疾病(COPD)现吸烟者和既往吸烟者中肺气肿的性别特异性特征。
Eur Respir J. 2016 Jan;47(1):104-12. doi: 10.1183/13993003.00996-2015. Epub 2015 Nov 5.
8
Clinical and Immunological Factors in Emphysema Progression. Five-Year Prospective Longitudinal Exacerbation Study of Chronic Obstructive Pulmonary Disease (LES-COPD).肺气肿进展中的临床和免疫因素。慢性阻塞性肺疾病五年前瞻性纵向加重研究(LES-COPD)。
Am J Respir Crit Care Med. 2015 Nov 15;192(10):1171-8. doi: 10.1164/rccm.201504-0736OC.
9
Effects of ageing and smoking on pulmonary computed tomography scans using parametric response mapping.使用参数反应映射研究衰老和吸烟对肺部计算机断层扫描的影响。
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Clinical and Radiologic Disease in Smokers With Normal Spirometry.肺功能正常的吸烟者的临床和放射学疾病
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吸烟者肺气肿和小气道疾病的进展

Progression of Emphysema and Small Airways Disease in Cigarette Smokers.

作者信息

Pompe Esther, Moore Camille M, Mohamed Hoesein Firdaus A A, de Jong Pim A, Charbonnier Jean-Paul, Han MeiLan K, Humphries Steven M, Hatt Charles R, Galbán Craig J, Silverman Ed K, Crapo James D, Washko George R, Regan Elisabeth A, Make Barry, Strand Matthew, Lammers Jan-Willem J, van Rikxoort Eva M, Lynch David A

机构信息

Imaging Department, University Medical Center Utrecht, Utrecht, the Netherlands.

Division of Biostatistics, Environment and Health, National Jewish Health, Denver, Colorado, United States.

出版信息

Chronic Obstr Pulm Dis. 2021 Apr 27;8(2):198-212. doi: 10.15326/jcopdf.2020.0140.

DOI:10.15326/jcopdf.2020.0140
PMID:33290645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8237975/
Abstract

BACKGROUND

Little is known about factors associated with emphysema progression in cigarette smokers. We evaluated factors associated with change in emphysema and forced expiratory volume in 1 second (FEV) in participants with and without chronic obstructive pulmonary disease (COPD).

METHODS

This retrospective study included individuals participating in the COPD Genetic Epidemiology study who completed the 5-year follow-up, including inspiratory and expiratory computed tomography (CT) and spirometry. All paired CT scans were analyzed using micro-mapping, which classifies individual voxels as emphysema or functional small airway disease (fSAD). Presence and progression of emphysema and FEV were determined based on comparison to nonsmoker values. Logistic regression analyses were used to identify clinical parameters associated with disease progression.

RESULTS

A total of 3088 participants were included with a mean ± SD age of 60.7±8.9 years, including 72 nonsmokers. In all Global initiative for chronic Obstructive Lung Disease (GOLD) stages, the presence of emphysema at baseline was associated with emphysema progression (odds ratio [OR]: GOLD 0: 4.32; preserved ratio-impaired spirometry [PRISm]; 5.73; GOLD 1: 5.16; GOLD 2: 5.69; GOLD 3/4: 5.55; all ≤0.01). If there was no emphysema at baseline, the amount of fSAD at baseline was associated with emphysema progression (OR for 1% increase: GOLD 0: 1.06; PRISm: 1.20; GOLD 1: 1.7; GOLD 3/4: 1.08; all ≤ 0.03).In 1735 participants without spirometric COPD, progression in emphysema occurred in 105 (6.1%) participants and only 21 (1.2%) had progression in both emphysema and FEV.

CONCLUSIONS

The presence of emphysema is an important predictor of emphysema progression. In patients without emphysema, fSAD is associated with the development of emphysema. In participants without spirometric COPD, emphysema progression occurred independently of FEV decline.

摘要

背景

关于吸烟者肺气肿进展的相关因素知之甚少。我们评估了慢性阻塞性肺疾病(COPD)患者和非COPD患者中与肺气肿变化及第一秒用力呼气容积(FEV)相关的因素。

方法

这项回顾性研究纳入了参与COPD遗传流行病学研究并完成5年随访的个体,包括吸气和呼气计算机断层扫描(CT)及肺功能测定。所有配对的CT扫描均使用微映射进行分析,该方法将各个体素分类为肺气肿或功能性小气道疾病(fSAD)。根据与非吸烟者值的比较确定肺气肿和FEV的存在及进展情况。采用逻辑回归分析来确定与疾病进展相关的临床参数。

结果

总共纳入了3088名参与者,平均年龄±标准差为60.7±8.9岁,其中包括72名非吸烟者。在所有慢性阻塞性肺疾病全球倡议(GOLD)阶段,基线时肺气肿的存在与肺气肿进展相关(优势比[OR]:GOLD 0期:4.32;肺功能正常-肺量计异常[PRISm]:5.73;GOLD 1期:5.16;GOLD 2期:5.69;GOLD 3/4期:5.55;均≤0.01)。如果基线时没有肺气肿,基线时fSAD的量与肺气肿进展相关(每增加1%的OR:GOLD 0期:1.06;PRISm:1.20;GOLD 1期:1.7;GOLD 3/4期:1.08;均≤0.03)。在1735名无肺功能测定COPD的参与者中,105名(6.1%)出现了肺气肿进展,只有21名(1.2%)肺气肿和FEV均有进展。

结论

肺气肿的存在是肺气肿进展的重要预测指标。在无肺气肿的患者中,fSAD与肺气肿的发生相关。在无肺功能测定COPD的参与者中,肺气肿进展独立于FEV下降而发生。