Abstract
Pulmonary hypertension (PH) is a common complication of chronic obstructive pulmonary disease (COPD) and is associated with increased morbidity and mortality. Reference standard method to diagnose PH is right heart catheterization. Several non-invasive imaging techniques have been employed in the detection of PH. Among them, computed tomography (CT) is the most commonly used for phenotyping and detecting complications of COPD. Several CT findings have also been described in patients with severe PH. Nevertheless, CT analysis is currently based on visual findings which can lead to reproducibility failure. Therefore, there is a need for quantification in order to assess objective criteria. In this review, progresses in automated analyses of CT parameters and their values in predicting PH and COPD outcomes are presented.
Keywords: computed tomography, pulmonary hypertension, COPD, prediction
Introduction
Chronic obstructive pulmonary disease (COPD) is a common, preventable and treatable disease that is characterized by persistent respiratory symptoms (ie, dyspnea, cough and/or sputum production) and airflow limitation that is due to airway and/or alveolar abnormalities usually caused by significant exposure to noxious particles or gases.1 COPD has an increasing prevalence worldwide and is mainly caused by tobacco smoke exposure. Diagnosis is based on spirometry with a post-bronchodilator FEV1/FVC ratio lower than 0.70.2 The level of COPD severity is now assessed using both functional (ie, FEV1 in percentage of predicted values) and clinical data (ie, symptoms scores (CAT and/or mMRC) and the number of exacerbations within the previous 12 months).2
COPD is frequently associated with comorbidities. Among them, pulmonary hypertension (PH) is causally related to COPD. PH is defined by a mean pulmonary arterial pressure (mPAP) equal or higher than 25 mmHg at rest, measured using the reference method right heart catheterization (RHC).3–6 The prevalence of PH and the underlying pathophysiologic processes in patients suffering from COPD remain unclear. Indeed, prevalence increases with COPD severity, and its rate has been reported varying from 20% to 90%.7–11 An increase of mPAP is associated with an increased number of hospitalizations, morbidity and mortality in COPD.12–15 The few patients with severe PH secondary to COPD, defined at RHC as a mPAP ≥35 mmHg or mPAP ≥25 with cardiac index (CI) <2 l/min/m2, are considered as a subgroup with potentially serious and high complication rate.5 So far, only a few studies have evaluated the effects of vasodilator in patients with severe PH secondary to COPD, meaning that this subpopulation might benefit from a specific care.16–18
There are no specific clinical symptoms of PH, and this complication starts insidiously, the most common symptom being dyspnea.8 PH in COPD patients has been shown to be associated with an increased exacerbation rate,8 worsen exercise capacity8 and a poorer prognosis.8,13,15 For instance in a study from Andersen et al,19 the survival rate was 63% for COPD patients without PH vs 37% in those with PH. The most reliable index of PH is the mPAP, a parameter so far measured only by RHC, an invasive technique which remains the reference method for the diagnosis of PH.3,4 This unique test enables a direct assessment of various pulmonary arterial pressure indices, systolic, diastolic, mean and capillary pressures, as well as resistance, cardiac output and therefore enables to differentiate pre- and post-capillary PH,20,21 a major way for assessing PH etiology. However, RHC can be responsible for the occurrence of adverse events, related to complication to venous access (such as hematoma, pneumothorax), but also those due to arrhythmias, hypotensive episodes due to vagal reaction or pulmonary vasoreactivity testing. Whereas RHC serious adverse events remain rare in experienced centers (ie, 1.1% and mortality is extremely rare),22 RHC is not totally safe, especially in unstable patients. Thus, noninvasive diagnosis techniques able to reduce the delay in diagnosing PH and to avoid side effects of RHC are suitable. Echocardiography has been proposed to evaluate systolic pulmonary arterial pressure (sPAP), which is correlated with mPAP, but its specificity is low.23 However, echocardiography remains the primary tool for patients screening, especially in others PH’s etiologies.4 Nevertheless, echocardiography may be technically difficult to perform, especially in patients with an inflated thorax and/or emphysema. Computed tomography (CT) is a common tool to investigate COPD and its role is crucial in the diagnosis and characterization of emphysema, airway disease, and advocated in various clinical situations such as follow-up, exacerbations, pre-operative surgery and lung transplantation.2,24–27 CT is a useful tool to assess in vivo observation; nevertheless, radiation exposure risk is not null;28 in addition, large inappropriate indications of this examination might lead to overrun radiology departments. Moreover, iodine contrast injection and repetitive CT acquisitions are needed to assess hemodynamic alterations related to PH which could increase risk of radiation and adverse reactions to contrast injection. Other interesting technics could be used to study PH, such as Dual energy CT,29 or magnetic resonance imaging (MRI). MRI is much less employed in lung diseases due to the low signal intensity of the lung but recent improvements have been published30–34 and MRI is currently the best tool for evaluating heart morphology and function,35 or estimating pulmonary arterial pressure using phase contrast MRI.36
CT is currently performed for screening PH etiology, notably in the assessment of chronic thromboembolic PH, lung disease, pulmonary arterial hypertension and pulmonary veno-occlusive disease.37–40 CT is also used as a prognostic marker in patients with PH.41
This review is focused on the role of CT in detecting PH in COPD patients. We will first describe the technical characteristics of CT and then we will discuss the morphological assessment of the parenchymal, bronchial and vascular compartments in COPD and their relationships with PH with a special interest in quantitative characterization.
COPD a multi-compartment disease
COPD is defined by functional irreversible airflow limitation but characteristic morphological changes are present in lung parenchyma, airways and pulmonary vasculature.1,42 Airflow limitation can be, at least partially, explained by parenchymal destruction due to emphysema.1 Emphysema is defined histologically by alveolar wall destruction and can be assessed visually using CT.43–45 The severity of emphysema can also be measured by quantitative CT indices reflecting the low attenuation area due to lung destruction. These quantitative indices have been shown to correlate with macroscopic and microscopic changes histologically.46,47
Proximal bronchial wall thickening is a common feature in COPD.48,49 Histological characteristics of proximal airways include increased infiltration of CD8(+) T lymphocytes, CD3+ T lymphocytes, macrophages.48–50 This thickening appeared to be more important in a particular COPD-phenotype characterized by less severe respiratory disease, older subjects and higher rates of obesity and cardiovascular comorbidities.51 Such a proximal thickening can be directly assessed by CT using 2D52,53 and 3D reconstruction.54–60
Bronchial wall thickening is however predominant in distal airways.61–65 At histological level, it associates luminal exudates, inflammatory cell infiltration and airway remodeling including peribronchial fibrosis, epithelial metaplasia, mucous gland hypertrophy and increased bronchial smooth muscle mass of the small airways.62,66 The higher the severity of COPD based on decreased FEV1, the higher the histological abnormalities.66 Moreover, inflammatory cell infiltration is related with tobacco smoking.67 A loss of small airways has been observed using microCT, a high-resolution imaging technique dedicated to small samples or animal models, contributing to airflow limitation.62 In humans, the small airway disease can be assessed two-folds morphologically: directly by showing centrilobular opacities and indirectly by using air trapping.67–69 Such an air trapping has been shown to correlate with the number of inflammatory cells (ie, neutrophils and mast cells) infiltrating the bronchial smooth muscle layer.67
It has been shown that the toxicity of tobacco smoke affects bronchi and parenchyma, but can also directly alter pulmonary vessels both in animals70 and humans.6,71 At histological level, pulmonary arterial remodeling appeared to be more important in COPD than in control subjects, and is particularly important in upper lobe and in small muscular pulmonary arteries.72 Those vessel alterations are multiples and can happen at initial stage of COPD71 with endothelial dysfunction, inflammation, suggesting that the history of PH in COPD might be related with cigarette-smoke-induced endothelial alterations.73,74 The quantitative amount of emphysema in COPD was often negatively correlated to pulmonary microvasculature abnormalities measured using CT,75–79 except for Wrobel et al,72 which did not find any significant correlation.
CT technical considerations
CT scan is the most reliable imaging modality for imaging pulmonary diseases, and it is available and commonly used in routine practice. The new generation of multidetector CT scanners allows acquisition of the whole lung in one breath hold with a submillimetric slice thickness and isotropic voxels using adequate matrix.
The COPD Gene study provides recommendations to standardize CT acquisition parameters in order to obtain high signal-to-noise ratio and accordingly accurate assessment of the images.80 Thin sections with non-contrast-enhanced volumetric acquisition is a standard technique for COPD imaging.81 However, intravenous iodinated contrast material is necessary in case of exacerbations or suspected pulmonary embolism. Standard reconstruction algorithm (smooth filter) is required for quantitative automatic analysis.82 Spirometric gated acquisition have been proposed to improve quantitative assessment, but is only used in dedicated research programs due to its complexity and low availability.83 Although COPD patients are older and radiation risks are thus minimized, balance between radiation dose and image quality should be considered. Misevaluation of quantitative parameters because of noisy images leads to standard tube parameters (kVp and mAs).84 However, low-dose CT acquisition with new iterative reconstruction algorithms allows noise reduction with acceptable quantitative measurements.83,85
Lung parenchyma
Historically, parenchymal alteration, and more precisely, emphysema, has been the first lung component investigated in order to explain PH in COPD. Indeed, emphysema is a major characteristic of COPD that could be quantified in patients when CT is performed. At CT, emphysema can be quantitatively evaluated, using low attenuation area percent (LAA%) derived from the voxel frequency distribution histogram. Several thresholds have been proposed but the most commonly employed is the value of –950 Hounsfield units (HU)45,46,86–89 (see Figure 1). It has been initially hypothesized that emphysema was correlated with mPAP. However, surprisingly, no relationship between PH and emphysema has been demonstrated neither in human nor in animal models.7,44,45,90,91 In addition, no significant difference in LAA% between COPD patients with or without PH was observed.45,92,93 Nonetheless, one single study observed that among COPD patients with PH, the LAA% measured using automated CT was correlated with right ventricular (RV) dysfunction.94 Emphysema can also be reflected using CT scan with the threshold of −960 HU, the evaluation of the first percentile,95 or in longitudinal studies, the 15th percentile is preferred to follow-up emphysema changes.96
Proximal bronchi
Bronchi can be studied using CT with 2D52,53 or 3D54–60 acquisitions. Various methods of bronchial segmentation and various parameters have been proposed, with so far no consensus (see Figure 2). Lumen area, wall area, wall area %, wall thickness and -Pi10, that reflects the normalized wall area of a theoretical 10-mm bronchi section area, have been proposed as indices for quantitating the severity of bronchial wall changes.45,52,86,89,97–101 We have demonstrated that bronchial thickness assessed by CT was increased in COPD patients with PH as compared to that of COPD patients without PH, whereas demographic, clinical and functional data (except PaO2 and 6 mins walk test distance, not surprisingly) remain unchanged.45 Moreover, a correlation between bronchial wall thickness and mPAP has been reported both in PH45 and in severe PH secondary to COPD.86,102 In addition, bronchial wall thickness measured using CT was correlated to histological measurements of airway remodeling,52 to exacerbation frequency,103 respiratory symptoms89 and to FEV1%.104
Small airways
Since obstruction of small airways, defined as airways with a diameter under 2 mm, has been shown to be the main determinant of obstruction in COPD,62–65 some imaging technics have intended to characterize small airway disease in COPD. Mosaic attenuation at inspiratory and air trapping at expiratory CT reflect small airway disease. Both are related to a decreased lung attenuation and therefore cannot be easily distinguished from emphysema.105 However, we have found that air trapping was correlated with inflammatory cell infiltration and might reflect peripheral airway obstruction in patients exposed to cigarette smoking.67 Galbán et al have assessed both expiratory and inspiratory CT using parametric response map in order to estimate functional small airway disease in COPD patients.106 Parametric response map was able to differentiate COPD phenotypes. In addition, Matsuoka et al calculated relative volume change (expiratory minus inspiratory relative volume) using CT with the threshold of −860 HU that was correlated with airway dysfunction (ie, assessed at PFTs) in COPD regardless of the degree of emphysema.68 To the best of our knowledge, there is no study dedicated to the small airways of COPD patients with PH using CT.
Central vessels
In COPD, a correlation has been shown between mPAP and enlargement of the main pulmonary artery truncus (MAP) diameter, and this increase is observed when MAP is normalized by ascending aorta diameter (MAP/AO).86,107–110 Usually, normalization is made on ascending aorta107,108,111,112 (see Figure 3) but it has also been done on descending aorta.21 Usually, MAP widest dimension is measured on axial CT images, on inspiratory acquisition, at bifurcation level, and, AO is measured on the same image.107,108,111,112 Descending aorta is also measured at the same level.112 Thresholds values to detect PH in COPD patients are: MAP ≥29 mm21,113,114 and MAP/AO>1.107,110,111,115,116
Increased MAP/AO ratio, a very simple index measured on a routine CT acquisition, has been shown linked to an increased risk of exacerbation in COPD108,111,117 and a lower 6-mins walk distance.118 Mortality in COPD population was also correlated to MAP/AO ratio in some reports115,119 but not in others.108,110 Interestingly, this ratio was not correlated to mortality in the general population.119 However, in healthy children, the ratio MAP/AO is higher than one, so the threshold of 1 cannot be applied in children.112
Pulmonary artery distensibility, that reflects elasticity using volume variations of the MAP between diastole and systole, is decreased in PH.3,4,120 The increase of stiffness is also observed in group 3 of PH121 and in PH related to COPD.122 Cardiac magnetic resonance (CMR) or ECG-gated CT can be also used to evaluate PA stiffness.3,4,120,121
In addition, dynamic-contrast-enhanced CT can be used to discriminate patients with or without PH from different etiology.123 A delayed flow of contrast and a reduced bolus propagation speed were observed in PH in comparison to control patients. Regions of interests were placed in the MAP and in the left and right pulmonary arteries. However, this study presented some limitations since bolus propagation also reflects the left heart function, the respiratory function and the speed of injection.123
Small vessels
The segmental pulmonary artery-to-bronchus ratio, semi-quantitatively evaluated for apical and posterior segments that run perpendicularly to the axial CT-scan, is positively correlated with mPAP.124 Ratio>1 in three or more lobes is specific of the presence of PH113,124 in group 3 of PH classification that also comprise COPD.125 In the same way, the size of the segmental arterial diameters is also positively correlated with mPAP124 in group 3 of PH.125
Regarding small pulmonary arteries, several of their characteristics have been studied, notably, number, volumes and areas. CT is an efficient tool in order to evaluate in vivo alterations of vessels, follow-up of illness or evaluating drug effects.
Some tools have been developed using 2D35,79,86,102 (see Figure 4) or 3D78,118,126 reconstructions.
Using 2D reconstruction on CT images, an automated measurement has been assessed using a free software Image J. These automated measurements allowed the visualization of small vessels alterations first on 3 CT slices44,127,128 and then on the whole lung.86,102 Software enables calculation of the percentage of cross-sectional areas (CSA%) of small pulmonary vessels under 5 mm2 (%CSA<5) and between 5 and 10 mm2 (CSA5–10), normalized by lung area, measuring subsubsegmental and subsegmental levels, respectively. Thus, in COPD patients without severe PH, the correlation between %CSA<5 and mPAP was negative44,86 whereas in COPD with severe PH correlation was positive.86,102
The 3D reconstruction technique allowed to measure volumes of small vessels.78,118,129 In both studies,78,118 index using 3D for assessment of pulmonary vessels was negatively correlated with MAP. For Ma et al,78 3D and 2D techniques were correlated. Studies using 2D and 3D are in the same line and showed a negative correlation between small pulmonary vessels and mPAP in COPD patients with most of the time moderate PH. As mentioned by others, all those vascular impairments support a vascular etiology of smoking-induced lung disease.6,130 CT metrics, such as %CSA<5, also allowed evaluation of the effect of pulmonary vasodilators in patients with PH related to COPD.79
In the automated measurements previously reported, pulmonary arteries were never separated from veins and this may affect the sensitivity of the technique. Tools have been developed in 3D in order to circumvent this limitation but not employed, to the best of our knowledge, for evaluating PH in COPD patients.126,129,131,132 A summary of vessels analyses is presented in Table 1.
Table 1.
Publication year | First author | Journal | CT findings | Qualitative /quantitative /Automated /manual | No. of patients | Screened population | Search for |
---|---|---|---|---|---|---|---|
2014 | Iyer et al107 | Chest | MAP/AO>1 better than echocardiography to evaluate PH in COPD patients | Quantitative manual | 60 | Severe COPD | mPAP ≥ 25 mmHg |
2017 | Iliaz S et al108 | Clin Respir J | MAP/AO correlated with PH, number of exacerbation, not with mortality | Quantitative manual | 156 | COPD exacerbation | Number of COPD exacerbation 1 year after the first one |
2017 | Cuttica MJ et al109 | Int J Chron Obstruct Pulmon Dis | MAP/AO associated with pulmonary hemodynamics and right heart structure and function changes | Semi-quantitative manual | 88 | Mil-to-moderately severe COPD | mPAP ≥ 25 mmHg |
2016 | Ortaç Ersoy E et al110 | J Crit Care | MAP/AO≥1 associated with pulmonary hypertension, but not with mortality | Quantitative manual | 106 | COPD | mPAP ≥ 25 mmHg |
2016 | Coste F et al86 | Thorax | % cross-sectional area of small pulmonary vessels <5 mm2 (%CSA<5) is negatively correlated to mPAP for moderated PH (25–35 mmHg), and positively correlated to mPAP for severe PH (>35 mmHg) | Quantitative automated | 105 | COPD | mPAP ≥ 25 mmHg 35 mmHg |
2012 | Wells JM et al111 | NEJM | MAP/AO>1 associated with severe COPD exacerbation | Quantitative manual | 3464 | Smokers with COPD | COPD exacerbation |
2015 | Compton GL et al112 | AJR | Description of technical measurements of MAP/AO in children, threshold is greater than 1, closer to 1.09 | Quantitative manual | 400 | General children population | Threshold of MAP/AO in children |
2011 | Chan AL et al21 | BMC Med Imaging | Significant predictors of PH: MAP≥ 29 mm, MAP/AO≥ 0.84, MAP/descending aorta≥ 1.29 mm | Quantitative manual | 101 | Heterogenous diagnoses | mPAP ≥ 25 mmHg |
1998 | Tan RT et al113 | Chest | MAP≥ 29 mm. Artery to bronchus ratio ≥1 in 3 or 4 lobes | Quantitative manual | 28 | Parenchymal lung disease | mPAP ≥ 20 mmHg |
2012 | Truong QA et al114 | Circ Cardiovasc Imaging | MAP≥ 29 mm in men, MAP≥ 27 mm in women, MAP/AO≥ 0.9 | Quantitative manual | 3171 | Asymptomatic community-based population | 90th percentile |
2014 | Shin S et al115 | Repir Med | MAP/AO>1 associated with PH in patients with COPD, independent predictor of mortality | Quantitative manual | 65 | Advanced COPD | mPAP ≥ 25 mmHg survival |
2016 | Mohamed Hoesein FA et al116 | Lung | MAP≥ 30 mm and MAP/AO> 1 associated with PH | Quantitative manual | 92 | COPD | mPAP ≥ 25 mmHg |
2016 | Wells JM et al117 | Chest | MAP/AO>1 predict exacerbation of COPD | Quantitative manual | 134 | Patient with acute exacerbation of COPD | Predict clinical outcome with MAP/AO |
2015 | Wells JM et al118 | Circ Cardiovasc Imaging | Intraparenchymal pulmonary blood vessel volume and the volume of distal vessels with cross-sectional area (CSA) of <5 mm2 negatively correlated with MAP/AO. MAP/AO, MAP negatively correlated with 6MWT | Quantitative automated | 24 | Non severe COPD | MAP/AO>1 |
2017 | Terzikhan N et al119 | Eur Respir J | In general population, MAP/AO >1 not associated with mortality. In COPD population, MAP/AO >1 associated with mortality | Quantitative manual | 2197 | General and COPD populations | Pronostic information of MAP/AO |
2009 | Revel MP et al120 | Radiology | Decreased pulmonary arterial distensibility in PH, ECG-gated CT | Quantitative manual | 45 | Different group 1, 2 etiology of PH | mPAP ≥ 25 mmHg |
2014 | Pienn M et al123 | Eur Radiol | Reduced bolus propagation speed and time differences between contrast material peaks in PH patients, using dynamic-contrast-enhanced CT | Quantitative semi-automated | 33 | Different potential etiology of PH, notably lung disease, and control patients | mPAP ≥ 25 mmHg |
2010 | Devaraj A et al124 | Radiology | MAP/AO and Artery to bronchus ratio correlated with mPAP | Quantitative manual | 77 | Spectrum of disease associated with PH (Groups 1, 3, 4,5) | mPAP ≥ 25 mmHg 34 mmHg |
Size of segmental arterial diameter correlated positively with mPAP | |||||||
2010 | Matsuoka S et al44 | Am J Respir Crit Care Med | % cross-sectional area of small pulmonary vessels <5 mm2 (%CSA<5) is negatively correlated to mPAP for moderated PH, in severe emphysema population | Quantitative automated | 79 | COPD | Correlation with mPAP |
2015 | Ando K et al79 | Lung | %CSA<5 used to assess pulmonary vasodilators longitudinal evaluation | Quantitative automated | 42 | COPD | Effect of pulmonary vasodilators in COPD-PH patients |
2017 | Ma J et al78 | J Xray Sci Technol | 3D tool able to detect the mean lumen area that was negatively correlated with MAP, and mean number of vessels negatively correlated with emphysema (LAA%, −950 HU) | Quantitative automated | 102 | Heavy smokers | Computerized scheme to detect pulmonary vessels |
2011 | Matsuoka S et al76 | Acad. Radiol. | Negative correlation between %CSA<5 and LAA% | Quantitative automated | 191 | Smoking history | Evaluate correlation small vessels- emphysema |
2011 | Uejima I et al128 | Jpn J Radiol | Positive correlation between %CSA<5 and FEV1/FVC | Quantitative automated | 30 | Non smokers | Evaluate correlation small vessels- PFTs |
2013 | Park S et al129 | Med Phys | Assessing volumetric technic allowing pulmonary artery/vein separation | Quantitative automated | 10 | COPD | Evaluate volumetric technic allowing pulmonary artery/vein separation |
2016 | Iyer S et al130 | Am J Respir Crit Care Med | After sildenafil arterial CSA and perfused blood volume decreased only in centriacinar emphysema patients, using dual-energy CT perfused blood volume | Quantitative automated | 17 | Current smokers | Effect of sildenafil on vascular perfusion |
2016 | Payer C et al131 | Med Image Anal | Assessing 3D technic allowing pulmonary artery/vein separation | Quantitative automated | 25 | Lung vascular disease | Evaluate 3D technic allowing pulmonary artery/vein separation |
2016 | Charbonnier JP et al132 | IEEE Trans Med Imaging | Automatic separation and classification of pulmonary arteries and veins using CT with an accuracy of 0.89 | Quantitative automated | 55 | Lung cancer | Evaluate separation and classification of pulmonary arteries/veins |
2019 | Coste F et al102 | Int J Chron Obstruct Pulmon Dis | % cross-sectional area of small pulmonary vessels <5 mm2 (%CSA<5) is positively correlated to mPAP for severe PH (>35 mmHg) | Quantitative automated | 24 | COPD | mPAP ≥35 mmHg |
Abbreviations: COPD, chronic obstructive pulmonary disease; CT, computed tomography; PH, pulmonary hypertension.
Scores
As mentioned above, several parameters reflecting various components in COPD are modified in COPD patients with PH. Building a score involving these parameters can be a strategy to improve the detection and the severity assessment of PH in COPD.
Tan et al have associated MAP ≥29 mm with artery-to-bronchus ratio >1 in 3 or 4 lobes and have reached a specificity of 100% for detecting PH in patients suffering from parenchymal lung diseases.113
Another index was composed of MAP/AO and right ventricular systolic pressure (RVSP) derived from echocardiography and was correlated with mPAP (R2=0.55)124 for group 1, 3, 4 and 5 of PH.3,4
Johns et al mentioned many RV parameters manually measured that are correlated with PH evolution in COPD patients.133 They tried to identify the best combination able to predict PH. First combination “cardiac magnetic resonance-RV” (“CMR-RV”) included RV mass and septal angle,134 second “CMR PA/RV” combined RV mass, septal angle and MAP measurements, and the third “α-index” encompass RV ejection fraction (RVEF) and minimal MAP size.135 The second model was the best model able to predict mPAP ≥25 mmHg. The same team also confirmed the interest of those results in another recent study using a validation cohort.136
We have built a “paw score” in order to predict severe PH in COPD patients combining CT automated measurements of bronchial wall thickness and pulmonary small vessels areas (%CSA<5) with PaO286,102
The various scores and their sensitivity are reported in Table 2.
Table 2.
Publication year | First author | Journal | Score | CT metrics | No. of patients | Screened population | Search for | Sens. Spe. | PPV NPV |
---|---|---|---|---|---|---|---|---|---|
1998 | Tan RT et al113 | Chest | MAP ≥29 mm + artery to bronchus ratio ≥1 in 3 or 4 lobes | MAP+A/B | 28 | Parenchymal lung disease | mPAP≥ 20 mmHg | NA 1.00 | NA |
2010 | Devaraj A et al124 | Radiology | MAP/AO + Right ventricular systolic pressure (echocardiography) | MAP/AO | 77 | Spectrum of disease associated with PH (Groups 1, 3, 4, 5) | mPAP≥ 25 mmHg 34 mmHg |
0.96 0.59 0.73 0.88 |
NA |
2016 | Coste F et al86 | Thorax | “Paw score”: %cross-sectional area of small pulmonary vessels <5 mm2+ bronchial wall thickening + PaO2 | %CSA<5+ WT | 105 | COPD | mPAP≥ 35 mmHg |
0.75 0.80 |
0.36 0.96 |
2019 | Coste F et al102 | Int J Chron Obstruct Pulmon Dis | “Paw score”: %cross-sectional area of small pulmonary vessels <5 mm2+ bronchial wall thickening + PaO2 | %CSA<5+ WT | 24 | COPD | mPAP≥ 35 mmHg |
0.88 NA |
NA NA |
2018 | Johns CS et al133 | Eur. Radio. | “CMR-RV”: RV mass + septal angle | 102 | COPD | mPAP≥ 25 mmHg |
0.90 0.79 |
0.96 0.58 |
|
“CMR-PA/RV”: RV mass + septal angle + MAP measurement | MAP measurement | 0.92 0.80 |
0.96 0.63 |
||||||
“α-index”: RV ejection fraction + minimal MAP size | Minimal MAP size | 1.00 0.13 |
0.87 1.00 |
||||||
Abbreviations: COPD, chronic obstructive pulmonary disease; CT, computed tomography; NA, not attributed; NPV, negative predictive value; PPV, predictive positive value; PH, pulmonary hypertension.
Conclusion
PH secondary to COPD is a serious complication that is important to predict with non-invasive tools. Integration of imaging into standard clinical practice is an asset for patient’s care. Automated measurements of markers reflecting pulmonary small vessels, bronchial wall and emphysema changes are emerging and might be used routinely in the future for predicting PH or severe PH. All these CT markers could be used in morpho-phenotyping studies. Further studies are required to assess their prognostic impact and follow-up under treatment.
Acknowledgment
This study has received funding from the Laboratory of Excellence TRAIL, ANR-10-LABX-57.
Abbreviations
AO, aorta; COPD, chronic obstructive pulmonary disease; CMR, cardiac magnetic resonance; CT, computed tomography; FEV1, forced expiratory volume in 1 second; FVC, forced volume capacity; HU, Hounsfield units; LAA%, low-attenuation area percentage; m, s, dPAP, mean, systolic, diastolic pulmonary arterial pressure; MAP, Main Pulmonary Artery truncus; MRI, magnetic resonance imaging; NA, not attributed; NPV, negative predictive value; PA, pulmonary artery; PaO2, arterial partial pressure of oxygen (mmHg); PFT: pulmonary Function test; PH, pulmonary hypertension; PPV, positive predictive value; RHC, right heart catheterization; RV, right ventricle; WA, bronchial Wall Area (mm); WT, mean bronchial Wall Thickness (mm); 6MWT, 6 mins walk tests; %CSA<5, percentage of total cross-sectional area of vessels less than 5 mm2 normalized by lung area.
Author contributions
All authors contributed to data analysis, drafting or revising the article, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.
Disclosure
Professor Laurent reports personal fees from Boehringer-Ingelheim, Roche, and Chiesi, outside the submitted work. Professor Pierre-Olivier Girodet reports personal fees, non-financial support from Novartis, personal fees, non-financial support from Chiesi, personal fees, non-financial support from Boehringer-Ingelheim, personal fees, non-financial support from AstraZeneca, personal fees, non-financial support from ALK, outside the submitted work. Professor Patrick Berger reports grants from Novartis, personal fees, non-financial support from AstraZeneca, personal fees, non-financial support from Menarini, personal fees, non-financial support from Circassia, personal fees, non-financial support from Sanofi, personal fees from Teva, outside the submitted work; in addition, Prof Berger has a patent Geometric characterization of airways using MRI. 22605-FR pending. The authors report no other conflicts of interest in this work.
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Data Citations
- From the Global Strategy for the Diagnosis, Management and Prevention of COPD, Global Initiative for Chronic Obstructive Lung Disease (GOLD); 2018. Available from: http://www.goldcopd.org/. Accessed July31, 2009.