4.7 Article

Cerebrovascular super-resolution 4D Flow MRI - Sequential combination of resolution enhancement by deep learning and physics-informed image processing to non-invasively quantify intracranial velocity, flow, and relative pressure

Journal

MEDICAL IMAGE ANALYSIS
Volume 88, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.media.2023.102831

Keywords

Super-resolution 4D flow MRI; Deep learning; Relative pressure; Cerebrovasculature

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The development of cerebrovascular disease is closely related to changes in intracranial flow and pressure. We developed a two-step approach using a deep residual network and physics-informed image processing to non-invasively quantify cerebrovascular hemodynamics. Our method showed good accuracy in estimating velocity and flow, as well as quantifying functional relative pressures. Additionally, we successfully applied our method to in-vivo volunteers, generating high-resolution intracranial flow images and reducing low-resolution bias in pressure estimation.
The development of cerebrovascular disease is tightly coupled to regional changes in intracranial flow and relative pressure. Image-based assessment using phase contrast magnetic resonance imaging has particular promise for non-invasive full-field mapping of cerebrovascular hemodynamics. However, estimations are complicated by the narrow and tortuous intracranial vasculature, with accurate image-based quantification directly dependent on sufficient spatial resolution. Further, extended scan times are required for high-resolution acquisitions, and most clinical acquisitions are performed at comparably low resolution (>1 mm) where biases have been observed with regard to the quantification of both flow and relative pressure. The aim of our study was to develop an approach for quantitative intracranial super-resolution 4D Flow MRI, with effective resolution enhancement achieved by a dedicated deep residual network, and with accurate quantification of functional relative pressures achieved by subsequent physics-informed image processing. To achieve this, our two-step approach was trained and validated in a patient-specific in-silico cohort, showing good accuracy in estimating velocity (relative error: 15.0 +/- 0.1%, mean absolute error (MAE): 0.07 +/- 0.06 m/s, and cosine similarity: 0.99 +/- 0.06 at peak velocity) and flow (relative error: 6.6 +/- 4.7%, root mean square error (RMSE): 0.56 mL/s at peak flow), and with the coupled physics-informed image analysis allowing for maintained recovery of functional relative pressure throughout the circle of Willis (relative error: 11.0 +/- 7.3%, RMSE: 0.3 +/- 0.2 mmHg). Furthermore, the quantitative super-resolution approach is applied to an in-vivo volunteer cohort, effectively generating intracranial flow images at <0.5 mm resolution and showing reduced low-resolution bias in relative pressure estimation. Our work thus presents a promising two-step approach to non-invasively quantify cerebrovascular hemodynamics, being applicable to dedicated clinical cohorts in the future.

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