HyperFitS -- Hypernetwork Fitting Spectra for metabolic quantification of ${}^1$H MR spectroscopic imaging

arXiv cs.LG / 4/6/2026

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Key Points

  • The paper introduces HyperFitS, a hypernetwork-based approach for fast metabolic quantification from whole-brain 1H MRSI spectra.
  • HyperFitS is designed to flexibly adapt to different baseline correction and water suppression settings, addressing a key limitation of less configurable neural network spectral fitting methods.
  • Experiments on human data acquired at 3T and 7T with multiple isotropic resolutions show strong agreement with conventional gold-standard LCModel fitting.
  • The method substantially reduces spectral fitting time from hours to a few seconds while maintaining accurate metabolite map outputs.
  • The study finds that baseline parametrization can change quantitative results by up to 30%, underscoring the importance of adaptable modeling in MRSI workflows.

Abstract

Purpose: Proton magnetic resonance spectroscopic imaging (^1H MRSI) enables the mapping of whole-brain metabolites concentrations in-vivo. However, a long-standing problem for its clinical applicability is the metabolic quantification, which can require extensive time for spectral fitting. Recently, deep learning methods have been able to provide whole-brain metabolic quantification in only a few seconds. However, neural network implementations often lack configurability and require retraining to change predefined parameter settings. Methods: We introduce HyperFitS, a hypernetwork for spectral fitting for metabolite quantification in whole-brain ^1H MRSI that flexibly adapts to a broad range of baseline corrections and water suppression factors. Metabolite maps of human subjects acquired at 3T and 7T with isotropic resolutions of 10 mm, 3.4 mm and 2 mm by water-suppressed and water-unsuppressed MRSI were quantified with HyperFitS and compared to conventional LCModel fitting. Results: Metabolic maps show a substantial agreement between the new and gold-standard methods, with significantly faster fitting times by HyperFitS. Quantitative results further highlight the impact of baseline parametrization on metabolic quantification, which can alter results by up to 30%. Conclusion: HyperFitS shows strong agreement with state-of-the-art conventional methods, while reducing processing times from hours to a few seconds. Compared to prior deep learning based spectral fitting methods, HyperFitS enables a wide range of configurability and can adapt to data quality acquired with multiple protocols and field strengths without retraining.