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Yongxian Qian

Publications and source records attributed to Yongxian Qian.

4 recordsLinked to original sources

Magnetic Field of Firing Neuron in Humans: Measurable by Quantum Sensing MRI?

Firing neurons generate action potentials that propagate along axons to transmit signals supporting cognitive functions. These electrical currents generate magnetic fields, yet direct detection of these neuronal magnetic fields by MRI remains elusive. This Mini Review investigates why this goal has been proven difficult to achieve and whether an emerging approach, quantum sensing MRI, can overcome the challenge.

physics.med-ph↗

Quantum Sensing MRI for Noninvasive Detection of Neuronal Electrical Activity in Human Brains

Neuronal electrical activity underlies human cognition including perception, attention, memory, language, and decision-making. Yet its direct, noninvasive measurement in the living human brain remains a fundamental challenge. Existing neuroimaging techniques, including electroencephalography (EEG), magnetoencephalography (MEG), and functional magnetic resonance imaging (fMRI), are limited by trade-offs in sensitivity and spatial or temporal resolution. Here we propose quantum sensing MRI (qsMRI), a noninvasive approach that enables direct detection of neuronal firing-induced magnetic fields using a clinical MRI system. qsMRI exploits endogenous proton (1H) nuclear spins in water molecules as intrinsic quantum sensors and decodes time-resolved phase information from the free induction decay signals to infer neuronal magnetic fields. We validate qsMRI through simulations, phantom experiments, and human studies at rest and during motor tasks, and provide open experimental procedures to facilitate independent rigorous validation. We further present a case study demonstrating potential applications to neurological disorders. qsMRI represents, to our knowledge, the first-in-human application of quantum sensing on a clinical MRI platform and may lay the foundation for a non-BOLD functional imaging modality capable of probing neuronal firing dynamics in both cortical and deep brain regions.

physics.med-ph↗

Multi-TE Single-Quantum Sodium (23Na) MRI: A Clinically Translatable Technique for Separation of Mono- and Bi-T2 Sodium Signals

Sodium magnetic resonance imaging (MRI) is sensitive and specific to ionic balance of cells owing to 10 fold difference in sodium concentration across membrane actively maintained by sodium potassium (Na+ K+) pump. Disruption of the pump and membrane integrity, as seen in neurological disorders such as epilepsy, multiple sclerosis, bipolar disease, and mild traumatic brain injury, leads to a large increase in intracellular sodium. Such a cellular level alteration is however overshadowed by large signal from extracellular sodium, leaving behind a long standing pursuit to separate signals from sodium exhibiting mono vs biexponential transverse (T2) decay under the inherent constraint of low signal to noise ratio even at advanced clinical field of 3 Tesla. Here we propose a novel technique that exploits intrinsic difference in their T2 decays by simply acquiring single quantum images at multiple echo times (TEs) and performing accurate matrix inversion at voxel. This approach was then investigated using numerical models, agar phantoms and human subjects, showing high accuracy of the separation in phantoms (95.8 percent for monoT2 and 72.5 to 80.4 percent for biT2) and clinical feasibility in humans. Thus, sodium MRI at 3T can now facilitate detection of neurological disorders early at cellular level and response to treatment as well. Keywords. sodium MRI, single quantum MRI, triple quantum MRI, neuroimaging, neurodegeneration

physics.med-ph↗

Resolution enhancement, noise suppression, and joint T2* decay estimation in dual-echo sodium-23 MR imaging using anatomically-guided reconstruction

Purpose: Sodium MRI is challenging because of the low tissue concentration of the 23 Na nucleus and its extremely fast biexponential transverse relaxation rate. In this article, we present an iterative reconstruction framework using dual-echo 23Na data and exploiting anatomical prior information (AGR) from high-resolution, low-noise, 1 H MR images. This framework enables the estimation and modeling of the spatially-varying signal decay due to transverse relaxation during readout (AGRdm), which leads to images of better resolution and reduced noise resulting in improved quantification of the reconstructed 23Na images. Methods: The proposed framework was evaluated using reconstructions of 30 noise realizations of realistic simulations of dual echo twisted projection imaging (TPI) 23 Na data. Moreover, three dual echo 23 Na TPI brain data sets of healthy controls acquired on a 3T Siemens Prisma system were reconstructed using conventional reconstruction, AGR and AGRdm. Results: Our simulations show that compared to conventional reconstructions, AGR and AGRdm show improved bias-noise characteristics in several regions of the brain. Moreover, AGR and AGRdm images show more anatomical detail and less noise in the reconstructions of the experimental data sets. Compared to AGR and the conventional reconstruction, AGRdm shows higher contrast in the sodium concentration ratio between gray and white matter and between gray matter and the brain stem. Conclusion: AGR and AGRdm generate 23 Na images with high resolution, high levels of anatomical detail, and low levels of noise, potentially enabling high-quality 23 Na MR imaging at 3T.

physics.med-ph↗