Generation of synthetic TSPO PET maps from structural MRI images.

IF 2.5 4区 医学 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Frontiers in Neuroinformatics Pub Date : 2025-09-08 eCollection Date: 2025-01-01 DOI:10.3389/fninf.2025.1633273
Matteo Ferrante, Marianna Inglese, Ludovica Brusaferri, Nicola Toschi, Marco L Loggia
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引用次数: 0

Abstract

Introduction: Neuroinflammation, a pathophysiological process involved in numerous disorders, is typically imaged using [11C]PBR28 (or TSPO) PET. However, this technique is limited by high costs and ionizing radiation, restricting its widespread clinical use. MRI, a more accessible alternative, is commonly used for structural or functional imaging, but when used using traditional approaches has limited sensitivity to specific molecular processes. This study aims to develop a deep learning model to generate TSPO PET images from structural MRI data collected in human subjects.

Methods: A total of 204 scans, from participants with knee osteoarthritis (n = 15 scanned once, 15 scanned twice, 14 scanned three times), back pain (n = 40 scanned twice, 3 scanned three times), and healthy controls (n = 28, scanned once), underwent simultaneous 3 T MRI and [11C]PBR28 TSPO PET scans. A 3D U-Net model was trained on 80% of these PET-MRI pairs and validated using 5-fold cross-validation. The model's accuracy in reconstructed PET from MRI only was assessed using various intensity and noise metrics.

Results: The model achieved a low voxel-wise mean squared error (0.0033 ± 0.0010) across all folds and a median contrast-to-noise ratio of 0.0640 ± 0.2500 when comparing true to reconstructed PET images. The synthesized PET images accurately replicated the spatial patterns observed in the original PET data. Additionally, the reconstruction accuracy was maintained even after spatial normalization.

Discussion: This study demonstrates that deep learning can accurately synthesize TSPO PET images from conventional, T1-weighted MRI. This approach could enable low-cost, noninvasive neuroinflammation imaging, expanding the clinical applicability of this imaging method.

Abstract Image

Abstract Image

Abstract Image

从结构MRI图像生成合成TSPO PET图。
神经炎症是一种涉及许多疾病的病理生理过程,通常使用[11C]PBR28(或TSPO) PET成像。然而,该技术受到高成本和电离辐射的限制,限制了其广泛的临床应用。MRI是一种更容易获得的替代方法,通常用于结构或功能成像,但当使用传统方法时,对特定分子过程的敏感性有限。本研究旨在开发一种深度学习模型,从人类受试者收集的结构MRI数据中生成TSPO PET图像。方法:共204例扫描,来自膝关节骨性关节炎(n = 15例扫描一次,15例扫描两次,14例扫描三次),背部疼痛(n = 40例扫描两次,3例扫描三次)和健康对照(n = 28例,扫描一次)的参与者同时进行了3次 T MRI和[11C]PBR28 TSPO PET扫描。3D U-Net模型在80%的PET-MRI对上进行训练,并使用5倍交叉验证进行验证。模型的准确性仅从MRI重建PET评估使用各种强度和噪声指标。结果:与真实重建PET图像相比,该模型在所有折叠中均方误差(0.0033 ± 0.0010)较低,中位对比噪声比为0.0640 ± 0.2500。合成的PET图像准确地复制了原始PET数据中观察到的空间模式。此外,即使在空间归一化后,重建精度仍保持不变。讨论:本研究表明,深度学习可以准确地从传统的t1加权MRI合成TSPO PET图像。该方法可以实现低成本、无创的神经炎症成像,扩大了该成像方法的临床适用性。
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来源期刊
Frontiers in Neuroinformatics
Frontiers in Neuroinformatics MATHEMATICAL & COMPUTATIONAL BIOLOGY-NEUROSCIENCES
CiteScore
4.80
自引率
5.70%
发文量
132
审稿时长
14 weeks
期刊介绍: Frontiers in Neuroinformatics publishes rigorously peer-reviewed research on the development and implementation of numerical/computational models and analytical tools used to share, integrate and analyze experimental data and advance theories of the nervous system functions. Specialty Chief Editors Jan G. Bjaalie at the University of Oslo and Sean L. Hill at the École Polytechnique Fédérale de Lausanne are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Neuroscience is being propelled into the information age as the volume of information explodes, demanding organization and synthesis. Novel synthesis approaches are opening up a new dimension for the exploration of the components of brain elements and systems and the vast number of variables that underlie their functions. Neural data is highly heterogeneous with complex inter-relations across multiple levels, driving the need for innovative organizing and synthesizing approaches from genes to cognition, and covering a range of species and disease states. Frontiers in Neuroinformatics therefore welcomes submissions on existing neuroscience databases, development of data and knowledge bases for all levels of neuroscience, applications and technologies that can facilitate data sharing (interoperability, formats, terminologies, and ontologies), and novel tools for data acquisition, analyses, visualization, and dissemination of nervous system data. Our journal welcomes submissions on new tools (software and hardware) that support brain modeling, and the merging of neuroscience databases with brain models used for simulation and visualization.
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