Abstract

Pulmonary hypertension (PH) can result in vascular pruning and increased tortuosity of the blood vessels. In this study we examined whether automatic extraction of lung vessels from contrast-enhanced thoracic computed tomography (CT) scans and calculation of tortuosity as well as 3D fractal dimension of the segmented lung vessels results in measures associated with PH.In this pilot study, 24 patients (18 with and 6 without PH) were examined with thorax CT following their diagnostic or follow-up right-sided heart catheterisation (RHC). Images of the whole thorax were acquired with a 128-slice dual-energy CT scanner. After lung identification, a vessel enhancement filter was used to estimate the lung vessel centerlines. From these, the vascular trees were generated. For each vessel segment the tortuosity was calculated using distance metric. Fractal dimension was computed using 3D box counting. Hemodynamic data from RHC was used for correlation analysis.Distance metric, the readout of vessel tortuosity, correlated with mean pulmonary arterial pressure (Spearman correlation coefficient: ρ = 0.60) and other relevant parameters, like pulmonary vascular resistance (ρ = 0.59), arterio-venous difference in oxygen (ρ = 0.54), arterial (ρ = −0.54) and venous oxygen saturation (ρ = −0.68). Moreover, distance metric increased with increase of WHO functional class. In contrast, 3D fractal dimension was only significantly correlated with arterial oxygen saturation (ρ = 0.47).Automatic detection of the lung vascular tree can provide clinically relevant measures of blood vessel morphology. Non-invasive quantification of pulmonary vessel tortuosity may provide a tool to evaluate the severity of pulmonary hypertension.Trial RegistrationClinicalTrials.gov NCT01607489

Highlights

  • Pulmonary hypertension (PH) is a chronic disorder of the pulmonary circulation, marked by an elevated vascular resistance and pressure

  • PH is defined as a mean pulmonary arterial pressure $25 mmHg, which is determined during invasive right heart catheterisation (RHC) [1,2]

  • The patient group consisted of 18 patients with PH (n = 4 with idiopathic pulmonary arterial hypertension (IPAH), n = 5 with associated pulmonary arterial hypertension (APAH), n = 2 with PH associated with lung disease, Table 2

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Summary

Introduction

Pulmonary hypertension (PH) is a chronic disorder of the pulmonary circulation, marked by an elevated vascular resistance and pressure This results in functional limitations, increased load on the right heart and may subsequently lead to right-heart failure [1]. Application of parallel computing algorithms on general purpose graphic processor units can lead to proper vessel segmentation through automatic processing of 3D volumetric CT data within a reasonable time [7,8]. This is a crucial step for the quantification of vascular measures in order to aid the diagnosis of vascular diseases [9,10]

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