Search bioRxiv⌕ Search

Biology subjects

Widmaier, M. S.

Publications and source records attributed to Widmaier, M. S..

2 recordsLinked to original sources

Single-shot simultaneous BOLD and velocity-encoding MRI for functional and slow-flow imaging

Cerebrospinal fluid (CSF) motion is coupled with global blood oxygenation level-dependent (BOLD) fluctuations, but the spatial relationship between regional brain activity and CSF dynamics remains poorly understood. Here, we developed a single-shot BOLD-VENC sequence that combines gradient-echo BOLD imaging with spin-echo velocity encoding following the same RF excitation, enabling simultaneous measurement of brain-wide BOLD activity and spatially resolved slow CSF velocity at 3T. The velocity measurement was validated in a slow-flow phantom and in five healthy participants using paced-breathing, breath-holding, and visual-stimulation experiments. Phantom measurements showed strong agreement with prescribed velocities over 0.1-1.0 mm/s (R2 = 0.93-0.98). In vivo measurements demonstrated respiratory- and cardiac-dependent changes in CSF velocity magnitude and direction across the ventricles and cortical subarachnoid spaces (SAS). The established coupling between the negative derivative of the global BOLD signal and fourth-ventricle CSF inflow was reproduced, with a peak lag of 0.9 s. Global BOLD fluctuations were also coupled with spatially distributed CSF velocity changes across ventricular and cortical CSF spaces, with a similar peak lag of 1.2 s. During visual checkerboard stimulation, BOLD-CSF velocity coupling was localized primarily to the SAS surrounding the activated visual cortex, demonstrating a regional relationship between local BOLD activity and nearby CSF motion. These findings establish the feasibility of simultaneous BOLD and slow CSF velocity imaging and extend BOLD-CSF coupling from a global measure toward spatially resolved assessment of hemodynamic-CSF interactions.

neuroscience↗

Time-efficient relaxation measurements by 31P MR fingerprinting in human brain at 7T

PurposeThe goal of the study is to develop 31P spectroscopic MRF at 7T to measure T1 and T2 relaxation times simultaneously and to compare time efficiency and test-retest reproducibility of MRF with conventional inversion recovery and multi-TE methods. MethodsA 31P MRF scheme was designed based on a balanced steady-state free precession type sequence. Dictionary was generated using the Bloch equations. B0 map was acquired experimentally and incorporated into the dictionary. 7 phantoms with different T1 and T2 relaxation times were prepared for MRF validation. Simulations were performed to evaluate estimation bias. 7 volunteers were scanned twice using both MRF and the conventional methods to evaluate the reproducibility. ResultsIn phantom measurements, T1 and T2 values between MRF and conventional methods demonstrated a good agreement with Pearsons correlation coefficients of 0.99 and 0.97, respectively. In in vivo experiments, estimated T1 by MRF were in good agreement with those measured by the inversion recovery and in the literature. On the other hand, estimated T2 values by MRF were shorter than those measured by the multi-TE method. 31P MRF method can reduce the acquisition time by 15 min providing less than 10% of mean CV for T1 estimations and less than 20% of mean CV for T2 estimations of metabolites. ConclusionOur results shows the feasibility of simultaneous T1 and T2 measurement of 31P metabolites in human brain using MRF at 7T. High reproducibility can be achieved especially for T1 measurement with 40% time reduction over conventional methods.

bioengineering↗