Abstract

This review is on the fast Padé transform (FPT) for magnetic resonance spectroscopy (MRS). It is structured into two portions. Firstly, we give an introductory overview, emphasizing the conceptual framework. Secondly, we cover the specific, concrete accomplishments with detailed analysis and selected illustrations. Key advances have been achieved by the FPT for MRS in the most recent period. These consist of direct applications of the FPT to time signals encoded by in vivo MRS from tumorous tissues. We focus on the robust and comprehensive Padé-based solutions for the thorniest problems (overlapping resonances, resolution, noise) that have hampered progress of in vivo MRS for a very long time. Both parametric and non-parametric aspects of signal processing in the FPT are thoroughly covered. The FPT, as a parameter estimator, solves exactly the quantification problem by reconstructing the positions, widths, heights and phases of all the physical peaks. This gives the component lineshapes of all the true resonances. The non-parametric FPT, as a shape estimator, has thus far predicted the total lineshapes alone without separating the individual components. Finally, we discuss the most recent advances in signal processing for MRS using the derivative fast Padé transform (dFPT). This upgrade is of utmost importance, as the dFPT exactly reconstructs all the peak parameters for every physical resonance by carrying out estimation of total shape spectra alone. The derivative operator within the dFPT narrows the linewidths and concomitantly enhances the peak heights, while simultaneously suppressing noise. This leads to separation of overlapping peaks, resolution improvement and noise reduction. Far-reaching ramifications of such an achievement within MRS are highlighted with the prospects for further explorations to the benefit particularly of cancer medicine.

Highlights

  • Basic sciences and their versatile applications are like two sides of the same coin

  • Spectra averaging and extrapolation for processing in vivo magnetic resonance spectroscopy (MRS) time signals encoded from the ovary In Ref. [11], we examined the role of spectra averaging in conjunction with Padébased extrapolation

  • Examination of spectral poles and zeros as the key to stability In a recent work [53], applying the fast Padé transform (FPT) to in vivo MRS time signals encoded from the ovary, we examined the essential features of the response function, namely both the spectral poles as well as the zeros, as the key to stability of the system to external perturbations

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Summary

Introduction

Basic sciences and their versatile applications are like two sides of the same coin. As an even more striking example, discovery of nuclear magnetic resonance (NMR) from the 1940s and 1950s in physics (Rabi, Bloch, ...) changed analytical chemistry forever in decrypting the structure of proteins and other big molecules (Ernst, Wutrich, ...). It revolutionized medicine, as well, through magnetic resonance spectroscopy (MRS) beginning already in the 1950s (Odenblad, ...) and magnetic resonance imaging (MRI) from the 1970s (Lauturber, Mansfield) for diagnostics, surgery and posttherapeutic follow-up. Lauturber (chemist) and Mansfield (physicist) shared the 2003 Nobel Prize on Medicine and Physiology for their contribution to the development of MRI

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