Bridging MRI and PET physiology: Untangling complementarity through orthogonal representations

arXiv cs.CV / 4/9/2026

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Key Points

  • The paper argues that multimodal MRI–PET fusion should explicitly distinguish shared information from modality-specific information, because this clarifies each modality’s irreducible clinical contribution and can guide acquisition design.
  • It proposes a subspace decomposition framework that treats fusion as orthogonal subspace separation (via representation geometry) rather than as simple latent translation between modalities.
  • Using multiparametric MRI to train a non-spatial implicit neural representation (INR) that predicts PSMA PET uptake, the method introduces SVD-based projection regularization to enforce orthogonality between an MRI-explainable physiological “envelope” and an orthogonal residual.
  • On 13 prostate cancer patients, the model shows that MRI-spanned components are absorbed into the learned envelope, while the orthogonal residual is strongest in tumor regions, implying PET contains signal aspects not recoverable from MRI-derived physiological descriptors.
  • The approach yields a structured, mathematically grounded characterization of complementarity between PSMA PET and MRI, focused on what each modality can or cannot represent.

Abstract

Multimodal imaging analysis often relies on joint latent representations, yet these approaches rarely define what information is shared versus modality-specific. Clarifying this distinction is clinically relevant, as it delineates the irreducible contribution of each modality and informs rational acquisition strategies. We propose a subspace decomposition framework that reframes multimodal fusion as a problem of orthogonal subspace separation rather than translation. We decompose Prostate-Specific Membrane Antigen (PSMA) PET uptake into an MRI-explainable physiological envelope and an orthogonal residual reflecting signal components not expressible within the MRI feature manifold. Using multiparametric MRI, we train an intensity-based, non-spatial implicit neural representation (INR) to map MRI feature vectors to PET uptake. We introduce a projection-based regularization using singular value decomposition to penalize residual components lying within the span of the MRI feature manifold. This enforces mathematical orthogonality between tissue-level physiological properties (structure, diffusion, perfusion) and intracellular PSMA expression. Tested on 13 prostate cancer patients, the model demonstrates that residual components spanned by MRI features are absorbed into the learned envelope, while the orthogonal residual is largest in tumour regions. This indicates that PSMA PET contains signal components not recoverable from MRI-derived physiological descriptors. The resulting decomposition provides a structured characterization of modality complementarity grounded in representation geometry rather than image translation.