4.5 Article

Robust arterial input function surrogate measurement from the superior sagittal sinus complex signal for fast dynamic contrast-enhanced MRI in the brain

期刊

MAGNETIC RESONANCE IN MEDICINE
卷 86, 期 6, 页码 3052-3066

出版社

WILEY
DOI: 10.1002/mrm.28922

关键词

arterial input function; brain perfusion; complex signal; dynamic contrast-enhanced MRI; inflow; superior sagittal sinus

资金

  1. Fonds de recherche du Quebec (FRQ)-Nature et technologies [2018-PR-206157]

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Accurately estimating the arterial input function for dynamic contrast-enhanced MRI is challenging due to signal magnitude changes often leading to underestimation of peak concentrations. A state-of-the-art complex-based method proposed in this study shows promising results in accurately determining the peak concentration by directly compensating for blood inflow and correcting signal phase. This method outperforms traditional magnitude- and phase-based methods in both simulated biases and patient data, providing a high-quality and robust estimation of the venous output function.
Purpose: Accurately estimating the arterial input function for dynamic contrast-enhanced MRI is challenging. An arterial input function is typically determined from signal magnitude changes related to a contrast agent, often leading to underestimation of peak concentrations. Alternatively, signal phase recovers the accurate peak concentration for straight vessels but suffers from high noise. A recent method proposed to fit the signal in the complex plane by combining the advantages of the previous 2 methods. The purpose of this work is to refine this complex-based method to determine the venous output function (VOF), an arterial input function surrogate, from the superior sagittal sinus. Methods: We propose a state-of-the-art complex-based method that includes direct compensation for blood inflow and signal phase correction accounting for the curvature of the superior sagittal sinus, generally assumed collinear with B-0. We compared the magnitude-, phase-, and complex-based VOF determination methods against various simulated biases as well as for 29 brain metastases patients. Results: Angulation of the superior sagittal sinus relative to B-0 varied widely within patients, and its effect on the signal phase caused an underestimation of peak concentrations of up to 65%. Correction significantly increased the VOF peak concentration for the phase-and complex-based VOFs in the cohort. The phase-based method recovered accurate peak concentrations but lacked precision in the tail of the VOF. Our complex-based VOF completely recovered the effect of inflow and resulted in a high-peak concentration with limited noise. Conclusion: The new complex-based method resulted in high-quality VOF robust against superior sagittal sinus curvature and variations in patient positioning.

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