Abstract
Objective
We conducted a meta‐analysis to systematic assess the diagnostic value of computed tomography (CT)‐based pulmonary artery to aorta (PA:A) ratio measurement in COPD with pulmonary hypertension (COPD‐PH).
Methods
Published studies referring to diagnostic accuracy of PA:A ratio for COPD‐PH were screened out from PubMed, Embase, Web of science, China National Knowledge databases (CNKI), Wan fang databases, and VIP databases. We used bivariate random‐effects model to estimate pooled sensitivity (SEN), specificity (SPE), positive and negative likelihood ratios (PLR and NLR, respectively), and diagnostic odds ratios (DOR). Summary receiver operating characteristic (SROC) curves and area under the curve (AUC) were also calculated to summarize the aggregate diagnostic performance.
Results
Nine eligible studies were included and the pooled SEN was 69% (95% CI: 59 ~ 78), SPE was 85% (95% CI: 77 ~ 90), PLR was 4.5 (95% CI: 2.8 ~ 7.5), and NLR was 0.36 (95% CI: 0.26 ~ 0.51), respectively. DOR reached 13.00 (95% CI: 6.00 ~ 28.00), and value of AUC was 0.84 (95% CI: 0.81 ~ 0.87). Subgroup analysis indicated that when the value of PA:A ratio was equal or greater than one (PA/A ≥ 1), the combined SEN, SPE, AUC, and DOR was 69%, 89%, 0.90, and 19.65, respectively.
Conclusions
PA:A ratio is helpful for appraisal of COPD‐PH, and PA/A ≥ 1 possessed prominent diagnostic accuracy.
Keywords: COPD, diagnostic accuracy, pulmonary artery to aorta ratio, pulmonary hypertension
We conducted a systematic review and meta‐analysis of available evidence on the accuracy of PA: A ratio for the diagnosis of pulmonary hypertension with COPD(COPD‐PH) and proved that CT‐based PA:A ratio measurement was a distinctively non‐invasive biomarker to complement diagnosis of COPD‐PH in the aspect of accuracy and specificity. Meanwhile, PA/A ≥ 1 may be an appropriate select.

1. INTRODUCTION
As a common chronic respiratory disease, chronic obstructive pulmonary disease (COPD) presents a condition with sophisticated clinical manifestations and pathophysiological features, which is featured with persistent respiratory symptoms and irreversible airflow limitation. 1
In addition to causing noteworthy economic and social burden, it was estimated that COPD would become the third leading cause of deaths globally in 2030. 2
The histological abnormality of COPD is the result of the combined action of many factors, such as small airway lesion, pulmonary parenchymal destruction, and pulmonary vascular reconsitution. 3 Cardiovascular comorbidities have a greater prevalence in COPD and associates with increased acute exacerbation and mortality, 4 which usually cannot be detected or estimated using conventional pulmonary function tests. Pulmonary hypertension (PH) occurs frequently across different stages of COPD, 5 especially in patients with advanced stage, and the prevalence rate of PH with COPD (COPD‐PH) has been reported varying from 20% to 90%. 6 PH is defined a mean pulmonary arterial pressure (mPAP) equal or higher than 25 mmHg at rest and measured by right heart catheterization (RHC). 7 , 8 However, as an invasive assessment method with numerous adverse complications, in fact, RHC cannot be widely popularized in clinical application. In contrast, comprehensive echocardiography is essential for screening and initial noninvasive assessment of PH. 9
Computed tomography (CT), a routine noninvasive check inspection device, has become a valuable technique for the assessment of morphological characteristics in COPD, such as emphysema, bronchial lesions, and pulmonary vessels, respectively. 10 , 11 , 12 A large prospective study showed that CT‐based pulmonary artery to aorta (PA:A) ratio on CT scan would be a remarkable parameter to predict the risk of COPD exacerbation and hospitalization. 13 Furthermore, the PA:A ratio has also been shown to outperform echocardiogram at predicting PH in patients with severe COPD. 14
To better accurately identify and select a distinctively characteristic sign of COPD‐PH, we undertook this systematic review and meta‐analysis to summarize the subsistent evidence on the accuracy of PA:A ratio for diagnosis of COPD‐PH.
2. METHODS
2.1. Publications selection
We searched PubMed, Embase, and Web of science with the search strategy of medical subject heading (MeSH) terms together with Entry Terms, which included “Chronic obstructive pulmonary disease,” “COPD,” “Computed Tomography,” “CT,” “pulmonary hypertension,” and “PH.” In the same way, databases of China National Knowledge Internet (CNKI), VIP, and Wan fang databases were searched as well. There were no restrictions in the date of publication and language.
The qualified study must involve in diagnostic accuracy of PA:A ratio for COPD‐PH, and all patients conformed to the diagnostic criteria of Global Initiative for Chronic Obstructive Lung Disease (GOLD) guideline, and the PH was diagnosed by RHC or echocardiography. The sensitivity (SEN) and specificity (SPE), meanwhile, were reported in the original research, or true negative (TN), true positive (TP), false negative (FN) and false positive (FP) can be calculated from the reported information. We excluded repetitive studies, animal research, reviews, case reporting, and literature with insufficient data. Two investigators (WXG and SYJ) independently retrieved eligible literature to preliminary analysis and reached an agreement.
2.2. Data extraction and quality assessment
The contents of the extraction information include first author, publication year, country, sample size, diagnostic apparatus, cut‐off value of PA:A ratio, and area under the receiver operating characteristic curve (AUC), SEN, and SPE of diagnostic accuracy. All eligible research was assessed with Quality Assessment of Diagnostic Accuracy Studies‐2 (QUADAS‐2) 15 criteria, which contained patient selection, index test, reference standard, flow, and timing. The included articles were evaluated as “low,” “high,” or “unclear” independently by two researchists and crosschecked.
2.3. Statistical analysis and data synthesis
The pooled estimates of SEN, SPE, and diagnostic odds ratio (DOR) were used to evaluate diagnostic value of PA:A ratio, and rational summary receiver operator characteristic (SROC) curve, AUC was assessed for diagnostic accuracy. Heterogeneity was quantified using Cochran's Q test, and P < 0.1 indicated as conspicuous heterogeneity. Commonly, the primary source of heterogeneity in test accuracy study is threshold effect. We therefore computed spearman correlation coefficient to reveal the threshold effect, if the coefficient showed strong negative correlation and P < 0.05, indicating the existence of threshold effect. 16 Deek's funnel plot asymmetry tests were conducted to assess publication bias. All data analyses were performed using STATA version 14 and Meta‐Disc version 1.4 statistical software.
3. RESULTS
3.1. Characteristics of included studies and quality assessment
A total of 1584 manuscripts were retrieved from published research. After eliminating of duplicates and reading of the titles/abstracts, we agreed on 36 articles meeting inclusive criteria to further browse the full text. Ultimately, nine retrospective studies 14 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 were taken into our review for further meta‐analysis (Figure 1), including 1238 COPD participants, of whom 548 patients were diagnosed as COPD‐PH. The patients with COPD‐PH in five studies were definite diagnosed according to RHC and the cut‐off value of CT‐based PA: A ratio was greater than or equal to one in six research (Table 1). Most of the studies had relatively low bias; however, there were problems in case selection and methodologic limitations, mainly due to unclear information, and the overall quality assessment results were shown in Figure 2.
FIGURE 1.

Following diagram illustrating study selection
TABLE 1.
Clinical characteristics of included studies
| Author | year | Country | Simple size | Golden standard | Technique | Cut‐off value of PA:A ratio | Grade of COPD | TP | FP | FN | TN | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| COPD‐PH | COPD | |||||||||||
| Shin et al. 18 | 2014 | America | 38 | 27 | RHC | LDCT | 1.00 | GOLD 3–4 | 19 | 2 | 19 | 25 |
| Iyer et al. 14 | 2014 | America | 22 | 38 | RHC | LDCT | 1.00 | GOLD 3–4 | 16 | 6 | 6 | 32 |
| Chen et al. 19 | 2015 | China | 56 | 165 | ECG | HRCT | 0.86 | NR | 32 | 51 | 24 | 114 |
| Mohamed et al. 20 | 2016 | Netherland | 30 | 62 | RHC | HRCT | 1.00 | GOLD 3–4 | 15 | 9 | 15 | 53 |
| Wang et al. 21 | 2018 | China | 37 | 56 | RHC | LDCT | 1.06 | NR | 24 | 9 | 13 | 47 |
| Tian and Wang 24 | 2016 | China | 55 | 55 | ECG | HRCT | 1.00 | NR | 51 | 2 | 4 | 53 |
| He et al. 22 | 2018 | China | 43 | 49 | ECG | LDCT | 1.00 | GOLD 1–2 | 30 | 3 | 13 | 46 |
| Lan 23 | 2019 | China | 174 | 195 | ECG | LDCT | 0.95 | GOLD 1–2 | 127 | 47 | 47 | 148 |
| Ratanawatkul et al. 17 | 2020 | America | 93 | 43 | RHC | HRCT | 0.90 | NR | 70 | 12 | 23 | 31 |
Abbreviations: COPD, chronic obstructive pulmonary disease; ECG, echocardiography; FN, false negative; FP, false positive; GOLD, Global Initiative for Chronic Obstructive Lung Disease; HRCT, high‐resolution computed tomography; LDCT, low‐dose computed tomography; NR, none report; PA:A, pulmonary artery/aorta ratio; PH, pulmonary hypertension; RCH, right heart catheterization; TN, true negative; TP, true positive.
FIGURE 2.

Methodological quality summary of individual studies
3.2. Diagnostic accuracy of PA/A for COPD‐PH
There was no threshold effect (r = −0.02, P = 0.95) according to spearman correlation coefficient but significant heterogeneity between different studies (Figure 3). Race, severity of COPD, inspection equipment of CT, golden standard, and the cut‐off value of PA/A were taken into account, and our meta‐regression analysis indicated that heterogeneity existed in the various cut‐off value of PA/A (PA/A ≥ 1 or <1) or other indeterminate covariates. The SEN was 69% (95% CI: 59 ~ 78), and SPE reached 85% (95% CI: 77 ~ 90). The pooled positive likelihood ratio (PLR) was 4.5 (95% CI: 2.8 ~ 7.5), and negative likelihood ratio (NLR) was 0.36 (95% CI: 0.26 ~ 0.51). The pooled DOR was estimated to 13.00 (95% CI: 6.00 ~ 28.00), and the AUC reached 0.84 (95% CI: 0.81 ~ 0.87) (Figure 4A). At the same time, the summary of subgroup analysis was reported in Table 2, and when the value of PA:A ratio was more than or equal to one (PA/A ≥ 1), the combined SEN, SPE, AUC, and DOR was 69%, 89%, 0.90, and 19.65, respectively (Figure 4B).
FIGURE 3.

Summary estimates of sensitivity and specificity with corresponding 95% CI for all of the studies (A) and subgroup analysis of PA/A ≥ 1 (B)
FIGURE 4.

Summary receiver operating characteristic curve (sROC) for all of the studies (A) and subgroup analysis of PA/A ≥ 1 (B)
TABLE 2.
Diagnostic accuracy summary of subgroup analysis
| Diagnostic Index | SEN (95%CI) | SPE (95%CI) | PLR (95%CI) | NLR (95%CI) | DOR (95%CI) | AUC (SE) |
|---|---|---|---|---|---|---|
| Cut‐off value | ||||||
| PA/A ≥ 1 | 0.69 (0.50–0.84) | 0.89 (0.84–0.93) | 6.06 (3.41–10.76) | 0.40 (0.23–0.56) | 19.65 (7.26–53.16) | 0.90 (0.05) |
| PA/A < 1 | 0.71 (0.66–0.76) | 0.73 (0.68–0.77) | 2.47 (1.76–3.46) | 0.42 (0.29–0.62) | 5.85 (2.93–11.68) | 0.80 (0.04) |
| Golden standard | ||||||
| RHC | 0.65 (0.59–0.72) | 0.83 (0.78–0.88) | 3.52 (2.59–4.77) | 0.45 (0.36–0.57) | 8.73 (5.46–13.95) | 0.81 (0.03) |
| ECG | 0.73 (0.68–0.78) | 0.78 (0.74–0.82) | 4.85 (2.18–10.80) | 0.31 (0.18–0.55) | 18.61 (4.63–74.74) | 0.83 (0.18) |
| Race | ||||||
| Asian | 0.72 (0.67–0.77) | 0.78 (0.75–0.82) | 4.51 (2.36–8.64) | 0.34 (0.22–0.53) | 15.55 (5.18–46.64) | 0.81 (0.16) |
| Others | 0.66 (0.58–0.72) | 0.83 (0.76–0.88) | 3.38 (2.39–4.78) | 0.46 (0.34–0.61) | 8.47 (4.97–14.46) | 0.81 (0.04) |
| Inspection equipment | ||||||
| HRCT | 0.72 (0.66–0.77) | 0.77 (0.72–0.82) | 3.69 (1.68–8.13) | 0.36 (0.19–0.66) | 11.92 (2.94–48.31) | 0.86 (0.15) |
| LDCT | 0.69 (0.63–0.74) | 0.82 (0.77–0.85) | 4.32 (2.82–6.63) | 0.40 (0.32–0.49) | 10.63 (7.08–15.96) | 0.80 (0.03) |
Abbreviations: AUC, area under the curve; DOR, diagnostic odds ratios; ECG, echocardiography; HRCT, high‐resolution computed tomography; LDCT, low‐dose computed tomography; NLR, negative likelihood ratios; PA/A, pulmonary artery/aorta ratio; PLR, positive likelihood ratios; RCH, right heart catheterization; SEN, pooled sensitivity; SPE, specificity.
3.3. Publication bias
The Deek's funnel plot asymmetry test was not statistically significant (P = 0.49) with a symmetrical funnel plot (Figure 5).
FIGURE 5.

Funnel plot for evaluation of publication bias in all studies
4. DISCUSSION
Our meta‐analysis of diagnostic accuracy to summarize related research evidence and proved that a CT‐based PA/A ≥ 1 presents a vital role in the diagnosis of COPD‐PH in the aspect of accuracy and SPE, which would be a valuable imaging marker to further assessment of COPD.
COPD possesses complex pathophysiological features, pulmonary ventilation dysfunction and hypoxia due to emphysema and airway inflammation can further trigger pulmonary vasoconstriction and remodeling, pulmonary vascular bed destruction, and increase pulmonary vascular resistance, resulting in PH. 25 , 26 In addition, certain global perspective research has revealed that about 30–70% of mild and moderate COPD patients accompanied PH, and a higher prevalence emerged in advanced COPD. 27 , 28 Therefore, early recognition of PH in patient with COPD is critical to the comprehensive management of COPD. In recent years, quite a number of studies have found that quantitative measurements of the PA:A ratio on pulmonary CT images in patients with COPD were helpful in identification of PH and closely associated with higher mortality, increased risk on exacerbations, and quality of life. 29 , 30 , 31 , 32 All these studies have also manifested a feasible noninvasive clinical tool for management of COPD‐PH.
In fact, a meta‐analysis had indicated that PA:A ratio suggested a moderate overall accuracy to distinguish PH in average patients, and value of AUC was 0.84. 33 However, we focused attention on the population of COPD and incorporated the existing research and proved that PA:A ratio indicated a better diagnostic effect of PH in patients with COPD in terms of the high value of AUC, especially when PA/A ≥ 1, the value reached 0.90. The random effects method, moreover, was performed to reckon the amalgamative SEN and SPE of SROC due to non‐negligible heterogeneity, and PA:A ratio was related to a high SPE, medium sensitivities in diagnosing of COPD‐PH, signifying a relative lower rate of misdiagnosis and high missed diagnosis. DOR is another indicator to evaluate the authenticity and reliability of diagnostic test, which reflects the degree of connection between the diagnostic index and the disease, and higher values mean better discriminatory test performance. The pooled DOR in our meta‐analysis was estimated as 19.65, indicating that PA:A ratio should be feasible index to the diagnosis of COPD‐PH.
The heterogeneity in these studies was explored through the meta‐regression analysis of possible influencing factors, such as Race, cut‐off value of PA:A ratio, severity of COPD, inspection equipment of CT, and golden standard; we found that the value of cut‐off may be a source of heterogeneity, especially when the PA/A value is bounded by one. At present, the optimum value of PA:A to discern COPD‐PH has not been affirmed; the cut‐off value ranges from 0.86 to 1.06 among our eligible studies. On the strength of our review, a higher SPE and diagnostic accuracy displayed when the value PA:A ratio was equal or greater than one, which highlighted a good discriminatory ability to COPD‐PH. For that matter, large prospective study should be conducted to further verification, and further research also showed a considerable screening value of PA:A ratio in patients with COPD‐PH whether using echocardiography or RHC as the gold standard. Meanwhile, in terms of diagnostic authenticity and SEN, the high‐resolution computed tomography (HRCT) examination present a more advantage from our subgroup analysis.
As a systematic review and meta‐analysis, we reviewed the previous research results and obtained valuable evidence‐based medicine testimony; however, limitations should not be neglected. First, a relatively small final included studies and existing of select bias in sectional studies that influenced the accuracy of the results. Moreover, there also was indecipherable heterogeneity among studies even though random‐effects model was used to amalgamate effect size.
5. CONCLUSIONS
In conclusion, CT‐based PA:A ratio measurement proved a noninvasive confirmatory test to complement diagnosis of COPD‐PH, and PA/A ≥ 1 may be an appropriate select.
CONFLICT OF INTEREST
The authors have no conflicts of interest to declare.
ETHICS STATEMENT
The ethical committee approval was not required at our institution because our research is a systematic review and meta‐analysis, and all analyses were based on previous published studies.
AUTHOR CONTRIBUTIONS
Xing‐gui Wu, Yu‐jia Shi, Xiao‐hua Wang, Xiao‐wei Yu performed the conceptualization. Xing‐gui Wu, Yu‐jia Shi, Xiao‐hua Wang, Ming‐xia Yang did the writing, original draft, systematic review, and meta‐analysis. Xiao‐hua Wang and Xiao‐wei Yu did the review and editing.
ACKNOWLEDGMENT
This study did not receive any funding.
Wu X, Shi Y, Wang X, Yu X, Yang M. Diagnostic value of computed tomography‐based pulmonary artery to aorta ratio measurement in chronic obstructive pulmonary disease with pulmonary hypertension: A systematic review and meta‐analysis. Clin Respir J. 2022;16(4):276-283. doi: 10.1111/crj.13485
Xing‐gui Wu and Yu‐jia Shi contributed equally to this study.
Contributor Information
Xiao‐hua Wang, Email: 3045220193@qq.com.
Xiao‐wei Yu, Email: czey1234@163.com.
DATA AVAILABILITY STATEMENT
The data that support the findings of this study are available from the corresponding author upon reasonable request.
REFERENCES
- 1. Global Strategy for the Diagnosis, Management and Prevention of Chronic Obstructive Pulmonary Disease 2020 Report. Available at: https://goldcopd.org/wp-content/uploads/2019/11/GOLD-2020-REPORT-ver1.owms. Accessed February 19, 2020. [Google Scholar]
- 2. Projections of Mortality and Causes of Death, 2016 and 2060. Available at: http://www.who.int/healthinfo/global_burden_disease/projections/en/. Accessed February 19, 2020. [Google Scholar]
- 3. O'Donnell DE, Laveneziana P, Webb K, Neder JA. Chronic obstructive pulmonary disease: clinical integrative physiology. Clin Chest Med. 2014;35(1):51‐69. [DOI] [PubMed] [Google Scholar]
- 4. Chen W, Thomas J, Sadatsafavi M, FitzGerald JM. Risk of cardiovascular comorbidity in patients with chronic obstructive pulmonary disease: a systematic review and meta‐analysis. Lancet Respir Med. 2015;3(8):631‐639. [DOI] [PubMed] [Google Scholar]
- 5. Blanco I, Piccari L, Barbera JA. Pulmonary vasculature in COPD: the silent component. Respirology. 2016;21(6):984‐994. [DOI] [PubMed] [Google Scholar]
- 6. Hoeper MM, Humbert M, Souza R, et al. A global view of pulmonary hypertension. Lancet Respir Med. 2016;4(4):306‐322. [DOI] [PubMed] [Google Scholar]
- 7. Kim D, George MP. Pulmonary hypertension. Med Clin North Am. 2019;103(3):413‐423. [DOI] [PubMed] [Google Scholar]
- 8. Mandras SA, Mehta HS, Vaidya A. Pulmonary hypertension: a brief guide for clinicians. Mayo Clin Proc. 2020;95(9):1978‐1988. [DOI] [PubMed] [Google Scholar]
- 9. Yaghi S, Novikov A, Trandafirescu T. Clinical update on pulmonary hypertension. J Investig Med. 2020;68(4):821‐827. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Mashimo S, Chubachi S, Tsutsumi A, et al. Relationship between diminution of small pulmonary vessels and emphysema in chronic obstructive pulmonary disease. Clin Imaging. 2017;46:85‐90. [DOI] [PubMed] [Google Scholar]
- 11. Bhatt SP, Washko GR, Hoffman EA, et al. Imaging advances in chronic obstructive pulmonary disease. Insights from the Genetic Epidemiology of Chronic Obstructive Pulmonary Disease (COPDGene) Study. Am J Respir Crit Care Med. 2019;199(3):286‐301. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Occhipinti M, Paoletti M, Bartholmai BJ, et al. Spirometric assessment of emphysema presence and severity as measured by quantitative CT and CT‐based radiomics in COPD. Respir Res. 2019;20(1):10‐11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Wells JM, Washko GR, Han MK, et al. Pulmonary arterial enlargement and acute exacerbations of COPD. N Engl J Med. 2012;367(10):913‐921. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Iyer AS, Wells JM, Vishin S, Bhatt SP, Wille KM, Dransfield MT. CT scan‐measured pulmonary artery to aorta ratio and echocardiography for detecting pulmonary hypertension in severe COPD. Chest. 2014;145(4):824‐832. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Whiting PF, Rutjes AW, Westwood ME, et al. QUADAS‐2: a revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med. 2011;155(8):529‐536. [DOI] [PubMed] [Google Scholar]
- 16. Arends LR, Hamza TH, van Houwelingen JC, Heijenbrok‐Kal MH, Hunink MGM, Stijnen T. Bivariate random effects meta‐analysis of ROC curves. Med Decis Mak. 2008;28:621‐638. [DOI] [PubMed] [Google Scholar]
- 17. Ratanawatkul P, Oh A, Richards JC, Swigris JJ. Performance of pulmonary artery dimensions measured on high‐resolution computed tomography scan for identifying pulmonary hypertension. ERJ Open Res. 2020;6(1):00232‐2019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Shin S, King CS, Brown AW, et al. Pulmonary artery size as a predictor of pulmonary hypertension and outcomes in patients with chronic obstructive pulmonary disease. Respir Med. 2014;108(11):1626‐1632. [DOI] [PubMed] [Google Scholar]
- 19. Chen XS, Liu K, Wang Z, et al. Computed tomography measurement of pulmonary artery for diagnosis of COPD and its comorbidity pulmonary hypertension. Int J Chron Obstruct Pulmon Dis. 2015;18(10):2525‐2533. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Mohamed FA, Besselink T, Pompe E, et al. Accuracy of CT pulmonary artery diameter for pulmonary hypertension in end‐stage COPD. Lung. 2016;194(5):813‐819. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. Wang Y, Wang HM, Gao YF, et al. Prediction value of plasma BNP and PA/A for pulmonary hypertension combined with COPD. Pract Pharm Clin Remedies. 2018;21(08):912‐916. [Google Scholar]
- 22. He JB, Wu HL, Zhou YJ. Diagnosis value of CT pulmonary artery diameter for pulmonary hypertension in COPD. Prevent Treat Cardio‐Cerebral‐Vascular Dis. 2018;18(6):452‐454. [Google Scholar]
- 23. Lan YX. Evaluation of pulmonary arterial hypertension in chronic obstructive pulmonary disease by chest CT. Ningxia: Medical University; 2019. [Google Scholar]
- 24. Tian HZ, Wang D. Diagnosis value of thoraco‐CT for the relevant pulmonary artery hypertension of COPD. Prac J Med Pharm. 2016;33(12):1081‐1084. [Google Scholar]
- 25. Ambatiello LG, Chazova IE. Cardiovascular and chronic obstructive pulmonary diseases: pathophysiological processes and treatment tactics. Ter Arkh. 2020;92(3):78‐83. [DOI] [PubMed] [Google Scholar]
- 26. Lindberg A, Linder R, Backman H, et al. From COPD epidemiology to studies of pathophysiological disease mechanisms: challenges with regard to study design and recruitment process: Respiratory and Cardiovascular Effects in COPD (KOLIN). Eur Clin Respir J. 2017;4(1):1415‐1095. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. Singh VK, George PM, Gries C. Pulmonary hypertension is associated with increased post‐lung transplant mortality risk in patients with chronic obstructive pulmonary disease. J Heart Lung Transplant. 2015;34(3):424‐429. [DOI] [PubMed] [Google Scholar]
- 28. Minai OA, Chaouat A, Adnot S. Pulmonary hypertension in COPD: epidemiology, significance, and management: pulmonary vascular disease: the global perspective. Chest. 2010;137(6):39S‐51S. [DOI] [PubMed] [Google Scholar]
- 29. Iliaz S, Tanriverdio E, Ozturk S, et al. Importance of pulmonary artery to ascending aorta ratio in chronic obstructive pulmonary disease. Clin Respir J. 2018;12(3):961‐965. [DOI] [PubMed] [Google Scholar]
- 30. Ortaç EE, Durusu TM, Öcal S, Akpinar MG, Topeli A. Measurement of pulmonary artery to aorta ratio in computed tomography is correlated with pulmonary artery pressure in critically ill chronic obstructive pulmonary disease patients. J Crit Care. 2016;33:42‐46. [DOI] [PubMed] [Google Scholar]
- 31. LaFon DC, Bhatt SP, Labaki WW, et al. Pulmonary artery enlargement and mortality risk in moderate to severe COPD: results from COPDGene. Eur Respir J. 2020;55:1901‐1812. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32. Ghobadi H, Janbazi H, Matin S, Lari SM, Ansarin K. The pulmonary artery‐aorta ratio: is it related to quality of life in chronic obstructive pulmonary disease?. Clin Respir J. 2018;12(8):2390‐2396. [DOI] [PubMed] [Google Scholar]
- 33. Shen Y, Wan C, Tian P, et al. CT‐base pulmonary artery measurement in the detection of pulmonary hypertension: a meta‐analysis and systematic review. Medicine. 2014;93(27):e256. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author upon reasonable request.
