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  • Open Access

Pulmonary arterial distensibility - 2D phase contrast vs 2D bSSFP

  • 1,
  • 1, 2,
  • 1,
  • 3 and
  • 1
Journal of Cardiovascular Magnetic Resonance201214 (Suppl 1) :P85

https://doi.org/10.1186/1532-429X-14-S1-P85

  • Published:

Keywords

  • Pulmonary Arterial Hypertension
  • Phase Contrast
  • Main Pulmonary Artery
  • Right Heart Catheterization
  • Arterial Distensibility

Summary

Main pulmonary artery distensibility is a strong predictor of mortality in patients with pulmonary arterial hypertension. This study shows that either 2D PC or 2D bSSFP can be used to reliably non-invasively assess it by measuring MPA relative area change.

Background

The pulmonary circulation is a highly compliant system that generates little resistance to blood flow. However, in the presence of pulmonary arterial hypertension (PAH), blood pressure and vascular resistance in the pulmonary circulation are elevated. This leads to distension and stiffening of the main pulmonary artery (MPA) and vessel wall remodeling, which in itself may influence stiffness [1]. Proximal arterial distensibility is a parameter that depends mainly on the anatomy (geometry) of the vessel and can be estimated noninvasively with cross-sectional imaging techniques. In particular, the relative area change (RAC) of the MPA, which is inversely proportional to arterial stiffness, is a strong predictor of mortality in patients with PAH [2]. The purpose of this study was to compare two non-invasive magnetic resonance imaging (MRI) methods for quantification of MPA distensibility using an acute PAH dog model.

Methods

Six adult female beagles were anesthetized with isoflurane. MRI was performed prior to and following injection of micro-beads into the right atrium and ventricle to induce PAH, resulting 12 comparison studies. The presence of PAH was confirmed by right heart catheterization (RHC). All MR images were acquired on a 3T scanner (MR750, GE Healthcare, Waukesha, WI). Double-oblique images perpendicular to the direction of the flow in the MPA were obtained using ECG-triggered 2D CINE balanced steady-state free precession (bSSFP) and through-plane velocity-encoded 2D phase contrast (PC) at the same level [3]. PC and bSSFP images were segmented using dedicated cardiovascular analysis software (CV-Flow and and MASS-Analysis, respectively, Medis, Leiden, NL). Maximum and minimum MPA areas (Amax and Amin, respectively) were used to calculate RAC = (Amax-Amin)/Amax. Bland-Altman analysis was used to study the differences between PC and bSSFP to calculate Amax, Amin, and RAC. Student t-test was used to evaluate statistical significance of the differences between techniques in all three paramenters.

Results

The mean values for RAC, Amax and Amin were 36.38±7.86%, 241.98±71.62cm2, and 157.06±58.51cm2 for PC, respectively and 31.14±6.95%, 220.88±62.76cm2, and 155.34±58.38cm2 for bSSFP, respectively (p=0.10, 0.45, and 0.94, respectively). The mean differences for RAC, Amax and Amin were -5.23±8.44%, -21.10±40.67cm2, -1.72±40.89cm2, respectively.

Conclusions

No statistically significant difference is present between PC and bSSFP for measuring RAC, Amax or Amin. The differences between the two methods for measuring these parameters are small suggesting that either technique (PC or bSSFP) can be used to reliably non-invasively measure MPA distensibility. A benefit of using PC for measuring RAC is that it can also be used to quantify blood flow.

Funding

University of Wisconsin - Madison, Department of Radiology, Research and Development fund.
Figure 1
Figure 1

2D bSSFP images (a. Amax and b. Amin) and 2DPC images (c.Amax and d. Amin).

Figure 2
Figure 2

Bland-Altman plot for comparison of MPA RAC measured with 2D PC and 2D bSSFP.

Authors’ Affiliations

(1)
Radiology, University of Wisconsin, Madison, WI, USA
(2)
Medical Physics, University of Wisconsin, Madison, WI, USA
(3)
Biomedical Engineering, University of Wisconsin, Madison, WI, USA

References

  1. Boerrigter B: Chest. 2010Google Scholar
  2. Gan C: Chest. 2007Google Scholar
  3. Herment A: MRM. 2011Google Scholar

Copyright

© Roldán-Alzate et al; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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